From 74ba4029f0160f0c4708a8c4b291c05184d3993d Mon Sep 17 00:00:00 2001 From: zsloan Date: Mon, 9 Nov 2015 17:38:50 +0000 Subject: Fixed issue that caused mapping to not work; for some reason the path to pylmm was wrong --- wqflask/base/data_set.py | 5 ++++- 1 file changed, 4 insertions(+), 1 deletion(-) (limited to 'wqflask/base') diff --git a/wqflask/base/data_set.py b/wqflask/base/data_set.py index d6a46c2e..5603fe2e 100755 --- a/wqflask/base/data_set.py +++ b/wqflask/base/data_set.py @@ -158,7 +158,10 @@ class Markers(object): """Todo: Build in cacheing so it saves us reading the same file more than once""" def __init__(self, name): json_data_fh = open(os.path.join(webqtlConfig.NEWGENODIR + name + '.json')) - markers = json.load(json_data_fh) + try: + markers = json.load(json_data_fh) + except: + markers = [] for marker in markers: if (marker['chr'] != "X") and (marker['chr'] != "Y"): -- cgit v1.2.3 From 933b90b8eba789dd89555ec31a6ff8db30808eac Mon Sep 17 00:00:00 2001 From: zsloan Date: Wed, 18 Nov 2015 17:04:54 +0000 Subject: Fixed issue where literature and tissue correlation didn't work Scatterplot matrix feature only appears if user is logged in now Committing current progress on mapping page (it can at least import the file now, but there are still errors) --- wqflask/base/mrna_assay_tissue_data.py | 10 +- .../wqflask/marker_regression/marker_regression.py | 12 +- .../marker_regression/marker_regression_gn1.py | 2745 ++++++++++++++++++++ .../wqflask/templates/marker_regression_gn1.html | 204 ++ .../templates/show_trait_statistics_new.html | 4 + wqflask/wqflask/views.py | 4 +- 6 files changed, 2969 insertions(+), 10 deletions(-) create mode 100644 wqflask/wqflask/marker_regression/marker_regression_gn1.py create mode 100644 wqflask/wqflask/templates/marker_regression_gn1.html (limited to 'wqflask/base') diff --git a/wqflask/base/mrna_assay_tissue_data.py b/wqflask/base/mrna_assay_tissue_data.py index 54a7ce8e..ba82057a 100755 --- a/wqflask/base/mrna_assay_tissue_data.py +++ b/wqflask/base/mrna_assay_tissue_data.py @@ -19,7 +19,7 @@ class MrnaAssayTissueData(object): if self.gene_symbols == None: self.gene_symbols = [] - print("self.gene_symbols:", self.gene_symbols) + #print("self.gene_symbols:", self.gene_symbols) self.data = collections.defaultdict(Bunch) @@ -57,9 +57,15 @@ class MrnaAssayTissueData(object): results = g.db.execute(query).fetchall() + lower_symbols = [] + for gene_symbol in gene_symbols: + if gene_symbol != None: + lower_symbols.append(gene_symbol.lower()) + for result in results: symbol = result[0] - if symbol.lower() in [gene_symbol.lower() for gene_symbol in gene_symbols]: + #if symbol.lower() in [gene_symbol.lower() for gene_symbol in gene_symbols]: + if symbol.lower() in lower_symbols: #gene_symbols.append(symbol) symbol = symbol.lower() diff --git a/wqflask/wqflask/marker_regression/marker_regression.py b/wqflask/wqflask/marker_regression/marker_regression.py index 553b4358..05bb5b60 100755 --- a/wqflask/wqflask/marker_regression/marker_regression.py +++ b/wqflask/wqflask/marker_regression/marker_regression.py @@ -75,6 +75,7 @@ class MarkerRegression(object): self.pair_scan = False # Initializing this since it is checked in views to determine which template to use self.score_type = "LRS" #ZS: LRS or LOD self.mapping_scale = "physic" + self.num_perm = 0 self.dataset.group.get_markers() if self.mapping_method == "gemma": @@ -94,7 +95,6 @@ class MarkerRegression(object): self.num_perm = start_vars['num_perm'] self.control = start_vars['control_marker'] self.do_control = start_vars['do_control'] - print("StartVars:", start_vars) self.method = start_vars['mapmethod_rqtl_geno'] self.model = start_vars['mapmodel_rqtl_geno'] @@ -102,7 +102,7 @@ class MarkerRegression(object): self.pair_scan = True results = self.run_rqtl_geno() - print("qtl_results:", results) + #print("qtl_results:", results) elif self.mapping_method == "plink": results = self.run_plink() #print("qtl_results:", pf(results)) @@ -163,8 +163,8 @@ class MarkerRegression(object): #Need to convert the QTL objects that qtl reaper returns into a json serializable dictionary for index, qtl in enumerate(self.qtl_results): - if index<40: - print("lod score is:", qtl['lod_score']) + #if index<40: + # print("lod score is:", qtl['lod_score']) if qtl['chr'] == highest_chr and highest_chr != "X" and highest_chr != "X/Y": print("changing to X") self.json_data['chr'].append("X") @@ -241,7 +241,7 @@ class MarkerRegression(object): included_markers.append(line.split("\t")[1]) p_values.append(float(line.split("\t")[10])) #p_values[line.split("\t")[1]] = float(line.split("\t")[10]) - print("p_values: ", p_values) + #print("p_values: ", p_values) return included_markers, p_values def gen_pheno_txt_file(self): @@ -784,7 +784,7 @@ class MarkerRegression(object): json_results = Redis.blpop("pylmm:results:" + temp_uuid, 45*60) results = json.loads(json_results[1]) p_values = [float(result) for result in results['p_values']] - print("p_values:", p_values[:10]) + #print("p_values:", p_values[:10]) #p_values = self.trim_results(p_values) t_stats = results['t_stats'] diff --git a/wqflask/wqflask/marker_regression/marker_regression_gn1.py b/wqflask/wqflask/marker_regression/marker_regression_gn1.py new file mode 100644 index 00000000..5deeb305 --- /dev/null +++ b/wqflask/wqflask/marker_regression/marker_regression_gn1.py @@ -0,0 +1,2745 @@ +# Copyright (C) University of Tennessee Health Science Center, Memphis, TN. +# +# This program is free software: you can redistribute it and/or modify it +# under the terms of the GNU Affero General Public License +# as published by the Free Software Foundation, either version 3 of the +# License, or (at your option) any later version. +# +# This program is distributed in the hope that it will be useful, +# but WITHOUT ANY WARRANTY; without even the implied warranty of +# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. +# See the GNU Affero General Public License for more details. +# +# This program is available from Source Forge: at GeneNetwork Project +# (sourceforge.net/projects/genenetwork/). +# +# Contact Drs. Robert W. Williams and Xiaodong Zhou (2010) +# at rwilliams@uthsc.edu and xzhou15@uthsc.edu +# +# +# +# This module is used by GeneNetwork project (www.genenetwork.org) +# +# Created by GeneNetwork Core Team 2010/08/10 +# +# Last updated by Zach 12/14/2010 + + +import time +import string +from math import * +import piddle as pid +import sys,os +import cPickle +import httplib, urllib + +from flask import Flask, g + +from htmlgen import HTMLgen2 as HT + +from utility import helper_functions +from utility import Plot +from base import webqtlConfig +#from intervalAnalyst import GeneUtil +#from base.webqtlTrait import webqtlTrait +#from base.templatePage import templatePage +#from utility import webqtlUtil +#from utility.THCell import THCell +#from utility.TDCell import TDCell +#from dbFunction import webqtlDatabaseFunction +#from base.GeneralObject import GeneralObject + +#import logging +#logging.basicConfig(filename="/tmp/gn_leiyan.log", level=logging.INFO) +#_log = logging.getLogger("gn\web\webqtl\intervalMapping\IntervalMappingPage.py") + +######################################### +# Inteval Mapping Plot Page +######################################### +class MarkerRegression(object): + cMGraphInterval = 5 + maxBootStrap = 50 + GRAPH_MIN_WIDTH = 900 + GRAPH_MAX_WIDTH = 10000 # Don't set this too high + GRAPH_DEFAULT_WIDTH = 1280 + MULT_GRAPH_DEFAULT_WIDTH = 2000 + MULT_GRAPH_MIN_WIDTH = 1400 + MULT_GRAPH_DEFAULT_WIDTH = 1600 + GRAPH_DEFAULT_HEIGHT = 600 + + + # Display order: + # UCSC BAND ========= + # ENSEMBL BAND -=-=-= + # ** GENES ********** + BAND_SPACING = 4 + + #ENSEMBL_BAND_Y = UCSC_BAND_Y + UCSC_BAND_HEIGHT + BAND_SPACING + UCSC_BAND_HEIGHT = 10 + ENSEMBL_BAND_HEIGHT = 10 + WEBQTL_BAND_HEIGHT = 10 + + #GENE_START_Y = ENSEMBL_BAND_Y + ENSEMBL_BAND_HEIGHT + BAND_SPACING + NUM_GENE_ROWS = 10 + EACH_GENE_HEIGHT = 6 # number of pixels tall, for each gene to display + EACH_GENE_ARROW_WIDTH = 5 + EACH_GENE_ARROW_SPACING = 14 + DRAW_DETAIL_MB = 4 + DRAW_UTR_LABELS_MB = 4 + + MIN_PIXELS_BETWEEN_LABELS = 50 + + qmarkImg = HT.Image('/images/qmarkBoxBlue.gif', width=10, height=13, border=0, alt='Glossary') + # Note that "qmark.gif" is a similar, smaller, rounded-edges question mark. It doesn't look + # like the ones on the image, though, which is why we don't use it here. + + HELP_WINDOW_NAME = 'helpWind' + + ## BEGIN HaplotypeAnalyst + NR_INDIVIDUALS = 0 + ## END HaplotypeAnalyst + + ALEX_DEBUG_BOOL_COLORIZE_GENES = 1 # 0=don't colorize, 1=colorize + ALEX_DEBUG_BOOL_PRINT_GENE_LIST = 1 + + kWIDTH_DEFAULT=1 + + kONE_MILLION = 1000000 + + LODFACTOR = 4.61 + + SNP_COLOR = pid.orange # Color for the SNP "seismograph" + TRANSCRIPT_LOCATION_COLOR = pid.mediumpurple + + GENE_FILL_COLOR = pid.HexColor(0x6666FF) + GENE_OUTLINE_COLOR = pid.HexColor(0x000077) + BOOTSTRAP_BOX_COLOR = pid.yellow + LRS_COLOR = pid.HexColor(0x0000FF) + LRS_LINE_WIDTH = 2 + SIGNIFICANT_COLOR = pid.HexColor(0xEBC7C7) + SUGGESTIVE_COLOR = pid.gainsboro + SIGNIFICANT_WIDTH = 5 + SUGGESTIVE_WIDTH = 5 + ADDITIVE_COLOR_POSITIVE = pid.green + ADDITIVE_COLOR_NEGATIVE = pid.red + ADDITIVE_COLOR = ADDITIVE_COLOR_POSITIVE + DOMINANCE_COLOR_POSITIVE = pid.darkviolet + DOMINANCE_COLOR_NEGATIVE = pid.orange + + ## BEGIN HaplotypeAnalyst + HAPLOTYPE_POSITIVE = pid.green + HAPLOTYPE_NEGATIVE = pid.red + HAPLOTYPE_HETEROZYGOUS = pid.blue + HAPLOTYPE_RECOMBINATION = pid.darkgray + ## END HaplotypeAnalyst + + QMARK_EDGE_COLOR = pid.HexColor(0x718118) + QMARK_FILL_COLOR = pid.HexColor(0xDEE3BB) + + TOP_RIGHT_INFO_COLOR = pid.black + X_AXIS_LABEL_COLOR = pid.black #HexColor(0x505050) + + MINI_VIEW_MAGNIFIED_REGION_COLOR = pid.HexColor(0xCC0000) + MINI_VIEW_OUTSIDE_REGION_COLOR = pid.HexColor(0xEEEEEE) + MINI_VIEW_BORDER_COLOR = pid.black + + CLICKABLE_WEBQTL_REGION_COLOR = pid.HexColor(0xF5D3D3) + CLICKABLE_WEBQTL_REGION_OUTLINE_COLOR = pid.HexColor(0xFCE9E9) + CLICKABLE_WEBQTL_TEXT_COLOR = pid.HexColor(0x912828) + + CLICKABLE_UCSC_REGION_COLOR = pid.HexColor(0xDDDDEE) + CLICKABLE_UCSC_REGION_OUTLINE_COLOR = pid.HexColor(0xEDEDFF) + CLICKABLE_UCSC_TEXT_COLOR = pid.HexColor(0x333366) + + CLICKABLE_ENSEMBL_REGION_COLOR = pid.HexColor(0xEEEEDD) + CLICKABLE_ENSEMBL_REGION_OUTLINE_COLOR = pid.HexColor(0xFEFEEE) + CLICKABLE_ENSEMBL_TEXT_COLOR = pid.HexColor(0x555500) + + GRAPH_BACK_LIGHT_COLOR = pid.HexColor(0xFBFBFF) + GRAPH_BACK_DARK_COLOR = pid.HexColor(0xF1F1F9) + + HELP_PAGE_REF = '/glossary.html' + + DRAW_UTR_LABELS=0 + + def __init__(self, start_vars): + + #templatePage.__init__(self, fd) + + #if not self.openMysql(): + # return + + #helper_functions.get_species_dataset_trait(self, start_vars) + + self.dataset = start_vars['dataset'] + self.this_trait = start_vars['this_trait'] + self.species = start_vars['species'] + + #ZS: Think I can just get all this from dataset object now + #RISet and Species + #if not fd.genotype: + # fd.readGenotype() + # + #fd.parentsf14regression = fd.formdata.getvalue('parentsf14regression') + # + #if ((fd.parentsf14regression == 'on') and fd.genotype_2): + # fd.genotype = fd.genotype_2 + #else: + # fd.genotype = fd.genotype_1 + #fd.strainlist = list(fd.genotype.prgy) + # + #self.species = webqtlDatabaseFunction.retrieveSpecies(cursor=self.cursor, RISet=fd.RISet) + + if self.dataset.species == "rat": + self._ucscDb = "rn3" + elif self.dataset.species == "mouse": + self._ucscDb = "mm9" + else: + self._ucscDb = "" + + ##################################### + # Options + ##################################### + #Mapping options + self.plotScale = start_vars['mapping_scale'] + #self.plotScale = fd.formdata.getvalue('scale', 'physic') + #if self.plotScale == 'physic' and not fd.genotype.Mbmap: #ZS: Not sure where "Mbmap" is stored, if at all; should be fine without this though + # self.plotScale = 'morgan' + if start_vars['num_perm'] != "": + self.nperm = int(start_vars['num_perm']) + else: + self.nperm = 0 + if (start_vars['num_perm'] == "") or (start_vars['num_perm'] < 1): + self.permChecked = False + else: + self.permChecked = True + #self.permChecked = fd.formdata.getvalue('permCheck', True) + self.bootChecked = False #ZS: For now setting to False, I'll add this option later once rest of figure works + #self.bootChecked = fd.formdata.getvalue('bootCheck', '') + if 'control' in start_vars.keys(): + self.controlLocus = start_vars['control'] + else: + self.controlLocus = "" + #self.controlLocus = fd.formdata.getvalue('controlLocus', '') + + #try: + # self.selectedChr = int(fd.formdata.getvalue('chromosomes', "-1")) + #except: + self.selectedChr = -1 + + #whether include parents and F1 for InbredSet + #fd.parentsf14regression = fd.formdata.getvalue('parentsf14regression') + #if ((fd.parentsf14regression == 'on') and fd.genotype_2): + # fd.genotype = fd.genotype_2 + #else: + # fd.genotype = fd.genotype_1 + + self.strainlist = self.dataset.group.samplelist + self.genotype = self.dataset.group.read_genotype_file() + + #Darwing Options + try: + if self.selectedChr > -1: + self.graphWidth = min(self.GRAPH_MAX_WIDTH, self.GRAPH_MIN_WIDTH) + else: + self.graphWidth = min(self.GRAPH_MAX_WIDTH, self.MULT_GRAPH_MIN_WIDTH) + except: + if self.selectedChr > -1: + self.graphWidth = self.GRAPH_DEFAULT_WIDTH + else: + self.graphWidth = self.MULT_GRAPH_DEFAULT_WIDTH + + #try: + # if self.selectedChr > -1: + # self.graphWidth = min(self.GRAPH_MAX_WIDTH, max(self.GRAPH_MIN_WIDTH, int(fd.formdata.getvalue('graphWidth')))) + # else: + # self.graphWidth = min(self.GRAPH_MAX_WIDTH, max(self.MULT_GRAPH_MIN_WIDTH, int(fd.formdata.getvalue('graphWidth')))) + #except: + # if self.selectedChr > -1: + # self.graphWidth = self.GRAPH_DEFAULT_WIDTH + # else: + # self.graphWidth = self.MULT_GRAPH_DEFAULT_WIDTH + +## BEGIN HaplotypeAnalyst + #self.haplotypeAnalystChecked = fd.formdata.getvalue('haplotypeAnalystCheck') + self.haplotypeAnalystChecked = False +## END HaplotypeAnalyst + + + self.graphHeight = self.GRAPH_DEFAULT_HEIGHT + self.additiveChecked = False + self.dominanceChecked = False + self.LRS_LOD = start_vars['score_type'] + self.intervalAnalystChecked = False + self.legendChecked = False + self.geneChecked = False + self.SNPChecked = False + self.draw2X = False + self.lrsMax = 0 + self.startMb = -1 + self.endMb = -1 + + #self.additiveChecked = fd.formdata.getvalue('additiveCheck') + #self.dominanceChecked = fd.formdata.getvalue('dominanceCheck') + #self.LRS_LOD = fd.formdata.getvalue('LRSCheck', 'LRS') + #self.intervalAnalystChecked = fd.formdata.getvalue('intervalAnalystCheck') + #self.legendChecked = fd.formdata.getvalue('viewLegend') + #self.geneChecked = fd.formdata.getvalue('showGenes') + #self.SNPChecked = fd.formdata.getvalue('showSNP') + #self.draw2X = fd.formdata.getvalue('draw2X') + #self.lrsMax = float(fd.formdata.getvalue('lrsMax', 0)) + #self.startMb = fd.formdata.getvalue('startMb', "-1") + #self.endMb = fd.formdata.getvalue('endMb', "-1") + + #try: + # self.startMb = float(self.startMb) + # self.endMb = float(self.endMb) + # if self.startMb > self.endMb: + # temp = self.startMb + # self.startMb = self.endMb + # self.endMb = temp + # #minimal distance 10bp + # if self.endMb - self.startMb < 0.00001: + # self.endMb = self.startMb + 0.00001 + #except: + # self.startMb = self.endMb = -1 + + #Trait Infos + self.identification = "" + #self.identification = fd.formdata.getvalue('identification', "") + + ################################################################ + # Generate Chr list and Retrieve Length Information + ################################################################ + self.ChrList = [("All", -1)] + for i, indChr in enumerate(self.genotype): + self.ChrList.append((indChr.name, i)) + + + + self.ChrLengthMbList = g.db.execute(""" + Select + Length from Chr_Length, InbredSet + where + Chr_Length.SpeciesId = InbredSet.SpeciesId AND + InbredSet.Name = '%s' AND + Chr_Length.Name in (%s) + Order by + Chr_Length.OrderId + """ % (self.dataset.group.name, string.join(map(lambda X: "'%s'" % X[0], self.ChrList[1:]), ", "))) + + self.ChrLengthMbList = map(lambda x: x[0]/1000000.0, self.ChrLengthMbList) + self.ChrLengthMbSum = reduce(lambda x, y:x+y, self.ChrLengthMbList, 0.0) + if self.ChrLengthMbList: + self.MbGraphInterval = self.ChrLengthMbSum/(len(self.ChrLengthMbList)*12) #Empirical Mb interval + else: + self.MbGraphInterval = 1 + + self.ChrLengthCMList = [] + for i, _chr in enumerate(self.genotype): + self.ChrLengthCMList.append(_chr[-1].cM - _chr[0].cM) + self.ChrLengthCMSum = reduce(lambda x, y:x+y, self.ChrLengthCMList, 0.0) + + if self.plotScale == 'physic': + self.GraphInterval = self.MbGraphInterval #Mb + else: + self.GraphInterval = self.cMGraphInterval #cM + + + + ################################################################ + # Get Trait Values and Infomation + ################################################################ + ##input from search page or selection page + #self.searchResult = fd.formdata.getvalue('searchResult') + ##convert single selection into a list + #if type("1") == type(self.searchResult): + # self.searchResult = string.split(self.searchResult,'\t') + # + #self.traitList = [] + #if self.searchResult and len(self.searchResult) > webqtlConfig.MULTIPLEMAPPINGLIMIT: + # heading = 'Multiple Interval Mapping' + # detail = ['In order to get clear result, do not select more than %d traits for \ + # Multiple Interval Mapping analysis.' % webqtlConfig.MULTIPLEMAPPINGLIMIT] + # self.error(heading=heading,detail=detail) + # return + #elif self.searchResult: + # self.dataSource = 'selectionPage' + # for item in self.searchResult: + # thisTrait = webqtlTrait(fullname=item, cursor=self.cursor) + # thisTrait.retrieveInfo() + # thisTrait.retrieveData(fd.strainlist) + # self.traitList.append(thisTrait) + #else: + + #input from data editing page + #fd.readData() + #if not fd.allTraitData: + # heading = "Mapping" + # detail = ['No trait data was selected for %s data set. No mapping attempted.' % fd.RISet] + # self.error(heading=heading,detail=detail) + # return + + self.dataSource = 'editingPage' + self.traitList = [] + thisTrait = start_vars['this_trait'] + #fullname = fd.formdata.getvalue('fullname', '') + #if fullname: + # thisTrait = webqtlTrait(fullname=fullname, data=fd.allTraitData, cursor=self.cursor) + # thisTrait.retrieveInfo() + #else: + # thisTrait = webqtlTrait(data=fd.allTraitData) + self.traitList.append(thisTrait) + + +## BEGIN HaplotypeAnalyst +## count the amount of individuals to be plotted, and increase self.graphHeight + #if self.haplotypeAnalystChecked and self.selectedChr > -1: + # thisTrait = self.traitList[0] + # _strains, _vals, _vars = thisTrait.exportInformative() + # smd=[] + # for ii, _val in enumerate(_vals): + # temp = GeneralObject(name=_strains[ii], value=_val) + # smd.append(temp) + # bxdlist=list(self.genotype.prgy) + # for j,_geno in enumerate (self.genotype[0][1].genotype): + # for item in smd: + # if item.name == bxdlist[j]: + # self.NR_INDIVIDUALS = self.NR_INDIVIDUALS + 1 +## default: + # self.graphHeight = self.graphHeight + 2 * (self.NR_INDIVIDUALS+10) * self.EACH_GENE_HEIGHT +## for paper: + # #self.graphHeight = self.graphHeight + 1 * self.NR_INDIVIDUALS * self.EACH_GENE_HEIGHT - 180 +## END HaplotypeAnalyst + + ################################################################ + # Calculations QTL goes here + ################################################################ + self.multipleInterval = len(self.traitList) > 1 + self.qtlresults = start_vars['qtl_results'] + #errorMessage = self.calculateAllResult(fd) + #if errorMessage: + # heading = "Mapping" + # detail = ['%s' % errorMessage] + # self.error(heading=heading,detail=detail) + # return + + if self.multipleInterval: + self.colorCollection = Plot.colorSpectrum(len(self.qtlresults)) + else: + self.colorCollection = [self.LRS_COLOR] + + + ######################### + ## Get the sorting column + ######################### + RISet = self.dataset.group.name + if RISet in ('AXB', 'BXA', 'AXBXA'): + self.diffCol = ['B6J', 'A/J'] + elif RISet in ('BXD', 'BXD300', 'B6D2F2', 'BDF2-2005', 'BDF2-1999', 'BHHBF2'): + self.diffCol = ['B6J', 'D2J'] + elif RISet in ('CXB'): + self.diffCol = ['CBY', 'B6J'] + elif RISet in ('BXH', 'BHF2'): + self.diffCol = ['B6J', 'C3H'] + elif RISet in ('B6BTBRF2'): + self.diffCol = ['B6J', 'BTB'] + elif RISet in ('LXS'): + self.diffCol = ['ILS', 'ISS'] + else: + self.diffCol= [] + + for i, strain in enumerate(self.diffCol): + self.diffCol[i] = g.db.execute("select Id from Strain where Symbol = %s", strain).fetchone()[0] + #self.cursor.execute("select Id from Strain where Symbol = %s", strain) + #self.diffCol[i] = self.cursor.fetchone()[0] + #print self.diffCol + + ################################################################ + # GeneCollection goes here + ################################################################ + if self.plotScale == 'physic': + #StartMb or EndMb + if self.startMb < 0 or self.endMb < 0: + self.startMb = 0 + self.endMb = self.ChrLengthMbList[self.selectedChr] + + geneTable = "" + + #if self.plotScale == 'physic' and self.selectedChr > -1 and (self.intervalAnalystChecked or self.geneChecked): + # chrName = self.genotype[0].name + # # Draw the genes for this chromosome / region of this chromosome + # if self.traitList and self.traitList[0] and len(self.traitList) == 1 and self.dataset.name: + # webqtldatabase = self.dataset.name + # #webqtldatabase = self.traitList[0].db.name + # else: + # webqtldatabase = None + # + # self.geneCol = None + # + # if self.species == "mouse": + # self.geneCol = GeneUtil.loadGenes(self.cursor, chrName, self.diffCol, self.startMb, self.endMb, webqtldatabase, "mouse") + # elif self.species == "rat": + # self.geneCol = GeneUtil.loadGenes(self.cursor, chrName, self.diffCol, self.startMb, self.endMb, webqtldatabase, "rat") + # else: + # self.geneCol = None + # + # if self.geneCol and self.intervalAnalystChecked: + # ####################################################################### + # #Nick use GENEID as RefGene to get Literature Correlation Informations# + # #For Interval Mapping, Literature Correlation isn't useful, so skip it# + # #through set GENEID is None # + # ####################################################################### + # + # #GENEID = fd.formdata.getvalue('GeneId') or None + # GENEID = None + # + # geneTableContainer = HT.Div(Id="sortable") #Div to hold table + # geneTable = self.geneTable(self.geneCol,GENEID) + # geneTableContainer.append(geneTable) + # + # mainfmName = webqtlUtil.genRandStr("fm_") + # tableForm = HT.Form(cgi=os.path.join(webqtlConfig.CGIDIR, webqtlConfig.SCRIPTFILE), enctype='multipart/form-data', name=mainfmName, submit=HT.Input(type='hidden')) + # tableForm.append(HT.Input(name='FormID', value='', type='hidden')) + # tableForm.append(geneTableContainer) + # + #else: + self.geneCol = None + + ################################################################ + # Plots goes here + ################################################################ + if self.plotScale != 'physic' or self.multipleInterval: + showLocusForm = webqtlUtil.genRandStr("fm_") + else: + showLocusForm = "" + intCanvas = pid.PILCanvas(size=(self.graphWidth,self.graphHeight)) + gifmap = self.plotIntMapping(intCanvas, startMb = self.startMb, endMb = self.endMb, showLocusForm= showLocusForm) + + filename= webqtlUtil.genRandStr("Itvl_") + intCanvas.save(os.path.join(webqtlConfig.IMGDIR, filename), format='png') + intImg=HT.Image('/image/'+filename+'.png', border=0, usemap='#WebQTLImageMap') + + #Scales plot differently for high resolution + if self.draw2X: + intCanvasX2 = pid.PILCanvas(size=(self.graphWidth*2,self.graphHeight*2)) + gifmapX2 = self.plotIntMapping(intCanvasX2, startMb = self.startMb, endMb = self.endMb, showLocusForm= showLocusForm, zoom=2) + intCanvasX2.save(os.path.join(webqtlConfig.IMGDIR, filename+"X2"), format='png') + #DLintImgX2=HT.Href(text='Download',url = '/image/'+filename+'X2.png', Class='smallsize', target='_blank') + + textUrl = self.writeQTL2Text(fd, filename) + + ################################################################ + # Info tables goes here + ################################################################ + #traitInfoTD = self.traitInfoTD(fd) + + #if self.draw2X: + # traitInfoTD.append(HT.P(), DLintImgX2, ' a higher resolution 2X image. ') + #else: + # traitInfoTD.append(HT.P()) + #if textUrl: + # traitInfoTD.append(HT.BR(), textUrl, ' results in tab-delimited text format.') + #traitRemapTD = self.traitRemapTD(self.cursor, fd) + #topTable = HT.TableLite(HT.TR(traitInfoTD, HT.TD(" ", width=25), traitRemapTD), border=0, cellspacing=0, cellpadding=0) + + ################################################################ + # Outputs goes here + ################################################################ + #this form is used for opening Locus page or trait page, only available for genetic mapping + if showLocusForm: + showLocusForm = HT.Form(cgi= os.path.join(webqtlConfig.CGIDIR, webqtlConfig.SCRIPTFILE), enctype='multipart/form-data', + name=showLocusForm, submit=HT.Input(type='hidden')) + hddn = {'FormID':'showDatabase', 'ProbeSetID':'_','database':fd.RISet+"Geno",'CellID':'_', 'RISet':fd.RISet, 'incparentsf1':'ON'} + for key in hddn.keys(): + showLocusForm.append(HT.Input(name=key, value=hddn[key], type='hidden')) + showLocusForm.append(intImg) + else: + showLocusForm = intImg + + if self.permChecked and not self.multipleInterval and 0 -1: + drawAreaHeight -= self.ENSEMBL_BAND_HEIGHT + self.UCSC_BAND_HEIGHT+ self.WEBQTL_BAND_HEIGHT + 3*self.BAND_SPACING+ 10*zoom + if self.geneChecked: + drawAreaHeight -= self.NUM_GENE_ROWS*self.EACH_GENE_HEIGHT + 3*self.BAND_SPACING + 10*zoom + else: + if self.selectedChr > -1: + drawAreaHeight -= 20 + else: + drawAreaHeight -= 30 + +## BEGIN HaplotypeAnalyst + if self.haplotypeAnalystChecked and self.selectedChr > -1: + drawAreaHeight -= self.EACH_GENE_HEIGHT * (self.NR_INDIVIDUALS+10) * 2 * zoom +## END HaplotypeAnalyst + + if zoom == 2: + drawAreaHeight -= 60 + + #Image map + gifmap = HT.Map(name='WebQTLImageMap') + + newoffset = (xLeftOffset, xRightOffset, yTopOffset, yBottomOffset) + # Draw the alternating-color background first and get plotXScale + plotXScale = self.drawGraphBackground(canvas, gifmap, offset=newoffset, zoom= zoom, startMb=startMb, endMb = endMb) + + #draw bootstap + #if self.bootChecked and not self.multipleInterval: + # self.drawBootStrapResult(canvas, fd.nboot, drawAreaHeight, plotXScale, offset=newoffset) + + # Draw clickable region and gene band if selected + if self.plotScale == 'physic' and self.selectedChr > -1: + self.drawClickBand(canvas, gifmap, plotXScale, offset=newoffset, zoom = zoom, startMb=startMb, endMb = endMb) + if self.geneChecked and self.geneCol: + self.drawGeneBand(canvas, gifmap, plotXScale, offset=newoffset, zoom = zoom, startMb=startMb, endMb = endMb) + if self.SNPChecked: + self.drawSNPTrackNew(canvas, offset=newoffset, zoom = 2*zoom, startMb=startMb, endMb = endMb) +## BEGIN HaplotypeAnalyst + if self.haplotypeAnalystChecked: + self.drawHaplotypeBand(canvas, gifmap, plotXScale, offset=newoffset, zoom = zoom, startMb=startMb, endMb = endMb) +## END HaplotypeAnalyst + # Draw X axis + self.drawXAxis(canvas, drawAreaHeight, gifmap, plotXScale, showLocusForm, offset=newoffset, zoom = zoom, startMb=startMb, endMb = endMb) + # Draw QTL curve + self.drawQTL(canvas, drawAreaHeight, gifmap, plotXScale, offset=newoffset, zoom= zoom, startMb=startMb, endMb = endMb) + + #draw legend + if self.multipleInterval: + self.drawMultiTraitName(fd, canvas, gifmap, showLocusForm, offset=newoffset) + elif self.legendChecked: + self.drawLegendPanel(fd, canvas, offset=newoffset, zoom = zoom) + else: + pass + + #draw position, no need to use a separate function + if self.genotype.Mbmap: + self.drawProbeSetPosition(canvas, plotXScale, offset=newoffset, zoom = zoom) + + return gifmap + + def drawBootStrapResult(self, canvas, nboot, drawAreaHeight, plotXScale, offset= (40, 120, 80, 10), zoom = 1, startMb = None, endMb = None): + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yZero = canvas.size[1] - yBottomOffset + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + + bootHeightThresh = drawAreaHeight*3/4 + + #break bootstrap result into groups + BootCoord = [] + i = 0 + startX = xLeftOffset + for j, _chr in enumerate(self.genotype): + BootCoord.append( []) + for _locus in _chr: + if self.plotScale == 'physic': + Xc = startX + (_locus.Mb-self.startMb)*plotXScale + else: + Xc = startX + (_locus.cM-_chr[0].cM)*plotXScale + BootCoord[-1].append([Xc, self.bootResult[i]]) + i += 1 + startX += (self.ChrLengthDistList[j] + self.GraphInterval)*plotXScale + + #reduce bootResult + if self.selectedChr > -1: + maxBootBar = 80.0 + else: + maxBootBar = 200.0 + stepBootStrap = plotWidth/maxBootBar + reducedBootCoord = [] + maxBootCount = 0 + + for BootChrCoord in BootCoord: + nBoot = len(BootChrCoord) + bootStartPixX = BootChrCoord[0][0] + bootCount = BootChrCoord[0][1] + for i in range(1, nBoot): + if BootChrCoord[i][0] - bootStartPixX < stepBootStrap: + bootCount += BootChrCoord[i][1] + continue + else: + if maxBootCount < bootCount: + maxBootCount = bootCount + # end if + reducedBootCoord.append([bootStartPixX, BootChrCoord[i][0], bootCount]) + bootStartPixX = BootChrCoord[i][0] + bootCount = BootChrCoord[i][1] + # end else + # end for + #add last piece + if BootChrCoord[-1][0] - bootStartPixX > stepBootStrap/2.0: + reducedBootCoord.append([bootStartPixX, BootChrCoord[-1][0], bootCount]) + else: + reducedBootCoord[-1][2] += bootCount + reducedBootCoord[-1][1] = BootChrCoord[-1][0] + # end else + if maxBootCount < reducedBootCoord[-1][2]: + maxBootCount = reducedBootCoord[-1][2] + # end if + for item in reducedBootCoord: + if item[2] > 0: + if item[0] < xLeftOffset: + item[0] = xLeftOffset + if item[0] > xLeftOffset+plotWidth: + item[0] = xLeftOffset+plotWidth + if item[1] < xLeftOffset: + item[1] = xLeftOffset + if item[1] > xLeftOffset+plotWidth: + item[1] = xLeftOffset+plotWidth + if item[0] != item[1]: + canvas.drawRect(item[0], yZero, item[1], yZero - item[2]*bootHeightThresh/maxBootCount, + fillColor=self.BOOTSTRAP_BOX_COLOR) + + ###draw boot scale + highestPercent = (maxBootCount*100.0)/nboot + bootScale = Plot.detScale(0, highestPercent) + bootScale = Plot.frange(bootScale[0], bootScale[1], bootScale[1]/bootScale[2]) + bootScale = bootScale[:-1] + [highestPercent] + + bootOffset = 50*fontZoom + bootScaleFont=pid.Font(ttf="verdana",size=13*fontZoom,bold=0) + canvas.drawRect(canvas.size[0]-bootOffset,yZero-bootHeightThresh,canvas.size[0]-bootOffset-15*zoom,yZero,fillColor = pid.yellow) + canvas.drawLine(canvas.size[0]-bootOffset+4, yZero, canvas.size[0]-bootOffset, yZero, color=pid.black) + canvas.drawString('0%' ,canvas.size[0]-bootOffset+10,yZero+5,font=bootScaleFont,color=pid.black) + for item in bootScale: + if item == 0: + continue + bootY = yZero-bootHeightThresh*item/highestPercent + canvas.drawLine(canvas.size[0]-bootOffset+4,bootY,canvas.size[0]-bootOffset,bootY,color=pid.black) + canvas.drawString('%2.1f'%item ,canvas.size[0]-bootOffset+10,bootY+5,font=bootScaleFont,color=pid.black) + + if self.legendChecked: + startPosY = 30 + nCol = 2 + smallLabelFont = pid.Font(ttf="trebuc", size=12*fontZoom, bold=1) + leftOffset = xLeftOffset+(nCol-1)*200 + canvas.drawRect(leftOffset,startPosY-6, leftOffset+12,startPosY+6, fillColor=pid.yellow) + canvas.drawString('Frequency of the Peak LRS',leftOffset+ 20, startPosY+5,font=smallLabelFont,color=pid.black) + + def drawProbeSetPosition(self, canvas, plotXScale, offset= (40, 120, 80, 10), zoom = 1, startMb = None, endMb = None): + if len(self.traitList) != 1: + return + + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yZero = canvas.size[1] - yBottomOffset + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + + try: + Chr = self.traitList[0].chr + Mb = self.traitList[0].mb + except: + return + + if self.plotScale == 'physic': + if self.selectedChr > -1: + if self.genotype[0].name != Chr or Mb < self.startMb or Mb > self.endMb: + return + else: + locPixel = xLeftOffset + (Mb-self.startMb)*plotXScale + else: + locPixel = xLeftOffset + for i, _chr in enumerate(self.genotype): + if _chr.name != Chr: + locPixel += (self.ChrLengthDistList[i] + self.GraphInterval)*plotXScale + else: + locPixel += Mb*plotXScale + break + else: + if self.selectedChr > -1: + if self.genotype[0].name != Chr: + return + else: + for i, _locus in enumerate(self.genotype[0]): + #the trait's position is on the left of the first genotype + if i==0 and _locus.Mb >= Mb: + locPixel=-1 + break + + #the trait's position is between two traits + if i > 0 and self.genotype[0][i-1].Mb < Mb and _locus.Mb >= Mb: + locPixel = xLeftOffset + plotXScale*(self.genotype[0][i-1].cM+(_locus.cM-self.genotype[0][i-1].cM)*(Mb -self.genotype[0][i-1].Mb)/(_locus.Mb-self.genotype[0][i-1].Mb)) + break + + #the trait's position is on the right of the last genotype + if i==len(self.genotype[0]) and Mb>=_locus.Mb: + locPixel = -1 + else: + locPixel = xLeftOffset + for i, _chr in enumerate(self.genotype): + if _chr.name != Chr: + locPixel += (self.ChrLengthDistList[i] + self.GraphInterval)*plotXScale + else: + locPixel += (Mb*(_chr[-1].cM-_chr[0].cM)/self.ChrLengthCMList[i])*plotXScale + break + if locPixel >= 0: + traitPixel = ((locPixel, yZero), (locPixel-6, yZero+12), (locPixel+6, yZero+12)) + canvas.drawPolygon(traitPixel, edgeColor=pid.black, fillColor=self.TRANSCRIPT_LOCATION_COLOR, closed=1) + + if self.legendChecked: + startPosY = 15 + nCol = 2 + smallLabelFont = pid.Font(ttf="trebuc", size=12*fontZoom, bold=1) + leftOffset = xLeftOffset+(nCol-1)*200*fontZoom + canvas.drawPolygon(((leftOffset+6, startPosY-6), (leftOffset, startPosY+6), (leftOffset+12, startPosY+6)), edgeColor=pid.black, fillColor=self.TRANSCRIPT_LOCATION_COLOR, closed=1) + canvas.drawString("Sequence Site", (leftOffset+15), (startPosY+5), smallLabelFont, self.TOP_RIGHT_INFO_COLOR) + + + def drawSNPTrackNew(self, canvas, offset= (40, 120, 80, 10), zoom = 1, startMb = None, endMb = None): + if self.plotScale != 'physic' or self.selectedChr == -1 or not self.diffCol: + return + + SNP_HEIGHT_MODIFIER = 18.0 + + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yZero = canvas.size[1] - yBottomOffset + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + + drawSNPLocationY = yTopOffset + plotHeight + chrName = self.genotype[0].name + + stepMb = (endMb-startMb)/plotWidth + strainId1, strainId2 = self.diffCol + SNPCounts = [] + + while startMb= %2.6f AND Mb < %2.6f AND + StrainId1 = %d AND StrainId2 = %d + """ % (chrName, startMb, startMb+stepMb, strainId1, strainId2)) + SNPCounts.append(self.cursor.fetchone()[0]) + startMb += stepMb + + if (len(SNPCounts) > 0): + maxCount = max(SNPCounts) + if maxCount>0: + for i in range(xLeftOffset, xLeftOffset + plotWidth): + snpDensity = float(SNPCounts[i-xLeftOffset]*SNP_HEIGHT_MODIFIER/maxCount) + canvas.drawLine(i, drawSNPLocationY+(snpDensity)*zoom, i, drawSNPLocationY-(snpDensity)*zoom, color=self.SNP_COLOR, width=1) + + def drawMultiTraitName(self, fd, canvas, gifmap, showLocusForm, offset= (40, 120, 80, 10), zoom = 1, locLocation= None): + nameWidths = [] + yPaddingTop = 10 + colorFont=pid.Font(ttf="trebuc",size=12,bold=1) + if len(self.qtlresults) >20 and self.selectedChr > -1: + rightShift = 20 + rightShiftStep = 60 + rectWidth = 10 + else: + rightShift = 40 + rightShiftStep = 80 + rectWidth = 15 + + for k, thisTrait in enumerate(self.traitList): + thisLRSColor = self.colorCollection[k] + kstep = k % 4 + if k!=0 and kstep==0: + if nameWidths: + rightShiftStep = max(nameWidths[-4:]) + rectWidth + 20 + rightShift += rightShiftStep + + name = thisTrait.displayName() + nameWidth = canvas.stringWidth(name,font=colorFont) + nameWidths.append(nameWidth) + + canvas.drawRect(rightShift,yPaddingTop+kstep*15, rectWidth+rightShift,yPaddingTop+10+kstep*15, fillColor=thisLRSColor) + canvas.drawString(name,rectWidth+2+rightShift,yPaddingTop+10+kstep*15,font=colorFont,color=pid.black) + if thisTrait.db: + + COORDS = "%d,%d,%d,%d" %(rectWidth+2+rightShift,yPaddingTop+kstep*15,rectWidth+2+rightShift+nameWidth,yPaddingTop+10+kstep*15,) + HREF= "javascript:showDatabase3('%s','%s','%s','');" % (showLocusForm, thisTrait.db.name, thisTrait.name) + Areas = HT.Area(shape='rect',coords=COORDS,href=HREF) + gifmap.areas.append(Areas) + + + def drawLegendPanel(self, fd, canvas, offset= (40, 120, 80, 10), zoom = 1, locLocation= None): + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yZero = canvas.size[1] - yBottomOffset + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + + + labelFont=pid.Font(ttf="trebuc",size=12*fontZoom, bold=1) + startPosY = 15 + stepPosY = 12*fontZoom + canvas.drawLine(xLeftOffset,startPosY,xLeftOffset+32,startPosY,color=self.LRS_COLOR, width=2) + canvas.drawString(self.LRS_LOD, xLeftOffset+40,startPosY+5,font=labelFont,color=pid.black) + startPosY += stepPosY + + if self.additiveChecked: + startPosX = xLeftOffset + canvas.drawLine(startPosX,startPosY,startPosX+17,startPosY,color=self.ADDITIVE_COLOR_POSITIVE, width=2) + canvas.drawLine(startPosX+18,startPosY,startPosX+32,startPosY,color=self.ADDITIVE_COLOR_NEGATIVE, width=2) + canvas.drawString('Additive Effect',startPosX+40,startPosY+5,font=labelFont,color=pid.black) + + if self.genotype.type == 'intercross' and self.dominanceChecked: + startPosX = xLeftOffset + startPosY += stepPosY + canvas.drawLine(startPosX,startPosY,startPosX+17,startPosY,color=self.DOMINANCE_COLOR_POSITIVE, width=4) + canvas.drawLine(startPosX+18,startPosY,startPosX+35,startPosY,color=self.DOMINANCE_COLOR_NEGATIVE, width=4) + canvas.drawString('Dominance Effect',startPosX+42,startPosY+5,font=labelFont,color=pid.black) + + if self.haplotypeAnalystChecked: + startPosY += stepPosY + startPosX = xLeftOffset + canvas.drawLine(startPosX,startPosY,startPosX+17,startPosY,color=self.HAPLOTYPE_POSITIVE, width=4) + canvas.drawLine(startPosX+18,startPosY,startPosX+35,startPosY,color=self.HAPLOTYPE_NEGATIVE, width=4) + canvas.drawLine(startPosX+36,startPosY,startPosX+53,startPosY,color=self.HAPLOTYPE_HETEROZYGOUS, width=4) + canvas.drawLine(startPosX+54,startPosY,startPosX+67,startPosY,color=self.HAPLOTYPE_RECOMBINATION, width=4) + canvas.drawString('Haplotypes (Pat, Mat, Het, Unk)',startPosX+76,startPosY+5,font=labelFont,color=pid.black) + + if self.permChecked: + startPosY += stepPosY + startPosX = xLeftOffset + canvas.drawLine(startPosX, startPosY, startPosX + 32, startPosY, color=self.SIGNIFICANT_COLOR, width=self.SIGNIFICANT_WIDTH) + canvas.drawLine(startPosX, startPosY + stepPosY, startPosX + 32, startPosY + stepPosY, color=self.SUGGESTIVE_COLOR, width=self.SUGGESTIVE_WIDTH) + lod = 1 + if self.LRS_LOD == 'LOD': + lod = self.LODFACTOR + canvas.drawString('Significant %s = %2.2f' % (self.LRS_LOD, self.significance/lod),xLeftOffset+42,startPosY +5,font=labelFont,color=pid.black) + canvas.drawString('Suggestive %s = %2.2f' % (self.LRS_LOD, self.suggestive/lod),xLeftOffset+42,startPosY + 5 +stepPosY,font=labelFont,color=pid.black) + + + + labelFont=pid.Font(ttf="verdana",size=12*fontZoom) + labelColor = pid.black + if self.selectedChr == -1: + string1 = 'Mapping for Dataset: %s, mapping on All Chromosomes' % fd.RISet + else: + string1 = 'Mapping for Dataset: %s, mapping on Chromosome %s' % (fd.RISet,self.genotype[0].name) + if self.controlLocus: + string2 = 'Using %s as control' % self.controlLocus + else: + string2 = 'Using Haldane mapping function with no control for other QTLs' + d = 4+ max(canvas.stringWidth(string1,font=labelFont),canvas.stringWidth(string2,font=labelFont)) + if fd.identification: + identification = "Trait ID: %s" % fd.identification + canvas.drawString(identification,canvas.size[0] - xRightOffset-d,20*fontZoom,font=labelFont,color=labelColor) + + canvas.drawString(string1,canvas.size[0] - xRightOffset-d,35*fontZoom,font=labelFont,color=labelColor) + canvas.drawString(string2,canvas.size[0] - xRightOffset-d,50*fontZoom,font=labelFont,color=labelColor) + + + def drawGeneBand(self, canvas, gifmap, plotXScale, offset= (40, 120, 80, 10), zoom = 1, startMb = None, endMb = None): + if self.plotScale != 'physic' or self.selectedChr == -1 or not self.geneCol: + return + + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yZero = canvas.size[1] - yBottomOffset + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + + yPaddingTop = yTopOffset + + displayStartInBases = startMb*self.kONE_MILLION + displayEndInBases = endMb*self.kONE_MILLION + + for gIndex, theGO in enumerate(self.geneCol): + geneNCBILink = 'http://www.ncbi.nlm.nih.gov/gene?term=%s' + if self.species == "mouse": + txStart = theGO["TxStart"] + txEnd = theGO["TxEnd"] + geneLength = (txEnd - txStart)*1000.0 + tenPercentLength = geneLength*0.0001 + SNPdensity = theGO["snpCount"]/geneLength + + exonStarts = map(float, theGO['exonStarts'].split(",")[:-1]) + exonEnds = map(float, theGO['exonEnds'].split(",")[:-1]) + cdsStart = theGO['cdsStart'] + cdsEnd = theGO['cdsEnd'] + accession = theGO['NM_ID'] + geneId = theGO['GeneID'] + geneSymbol = theGO["GeneSymbol"] + strand = theGO["Strand"] + exonCount = theGO["exonCount"] + + geneStartPix = xLeftOffset + plotXScale*(float(txStart) - startMb) + geneEndPix = xLeftOffset + plotXScale*(float(txEnd) - startMb) #at least one pixel + + if (geneEndPix < xLeftOffset): + return; # this gene is not on the screen + elif (geneEndPix > xLeftOffset + plotWidth): + geneEndPix = xLeftOffset + plotWidth; # clip the last in-range gene + if (geneStartPix > xLeftOffset + plotWidth): + return; # we are outside the valid on-screen range, so stop drawing genes + elif (geneStartPix < xLeftOffset): + geneStartPix = xLeftOffset; # clip the first in-range gene + + #color the gene based on SNP density + + + #found earlier, needs to be recomputed as snps are added + + #always apply colors now, even if SNP Track not checked - Zach 11/24/2010 + + densities=[1.0000000000000001e-05, 0.094094033555233408, 0.3306166377816987, 0.88246026851027781, 2.6690084029581951, 4.1, 61.0] + if SNPdensity < densities[0]: + myColor = pid.black + elif SNPdensity < densities[1]: + myColor = pid.purple + elif SNPdensity < densities[2]: + myColor = pid.darkblue + elif SNPdensity < densities[3]: + myColor = pid.darkgreen + elif SNPdensity < densities[4]: + myColor = pid.gold + elif SNPdensity < densities[5]: + myColor = pid.darkorange + else: + myColor = pid.darkred + + outlineColor = myColor + fillColor = myColor + + TITLE = "Gene: %s (%s)\nFrom %2.3f to %2.3f Mb (%s)\nNum. exons: %d." % (geneSymbol, accession, float(txStart), float(txEnd), strand, exonCount) + # NL: 06-02-2011 Rob required to change this link for gene related + HREF=geneNCBILink %geneSymbol + + elif self.species == "rat": + exonStarts = [] + exonEnds = [] + txStart = theGO["TxStart"] + txEnd = theGO["TxEnd"] + cdsStart = theGO["TxStart"] + cdsEnd = theGO["TxEnd"] + geneId = theGO["GeneID"] + geneSymbol = theGO["GeneSymbol"] + strand = theGO["Strand"] + exonCount = 0 + + geneStartPix = xLeftOffset + plotXScale*(float(txStart) - startMb) + geneEndPix = xLeftOffset + plotXScale*(float(txEnd) - startMb) #at least one pixel + + if (geneEndPix < xLeftOffset): + return; # this gene is not on the screen + elif (geneEndPix > xLeftOffset + plotWidth): + geneEndPix = xLeftOffset + plotWidth; # clip the last in-range gene + if (geneStartPix > xLeftOffset + plotWidth): + return; # we are outside the valid on-screen range, so stop drawing genes + elif (geneStartPix < xLeftOffset): + geneStartPix = xLeftOffset; # clip the first in-range gene + + outlineColor = pid.darkblue + fillColor = pid.darkblue + TITLE = "Gene: %s\nFrom %2.3f to %2.3f Mb (%s)" % (geneSymbol, float(txStart), float(txEnd), strand) + # NL: 06-02-2011 Rob required to change this link for gene related + HREF=geneNCBILink %geneSymbol + else: + outlineColor = pid.orange + fillColor = pid.orange + TITLE = "Gene: %s" % geneSymbol + + #Draw Genes + geneYLocation = yPaddingTop + (gIndex % self.NUM_GENE_ROWS) * self.EACH_GENE_HEIGHT*zoom + + if 1:#drawClickableRegions: + geneYLocation += self.UCSC_BAND_HEIGHT + self.BAND_SPACING + self.ENSEMBL_BAND_HEIGHT + self.BAND_SPACING + self.WEBQTL_BAND_HEIGHT + self.BAND_SPACING + else: + geneYLocation += self.BAND_SPACING + + #draw the detail view + if self.endMb - self.startMb <= self.DRAW_DETAIL_MB and geneEndPix - geneStartPix > self.EACH_GENE_ARROW_SPACING * 3: + utrColor = pid.Color(0.66, 0.66, 0.66) + arrowColor = pid.Color(0.7, 0.7, 0.7) + + #draw the line that runs the entire length of the gene + #canvas.drawString(str(geneStartPix), 300, 400) + canvas.drawLine(geneStartPix, geneYLocation + self.EACH_GENE_HEIGHT/2*zoom, geneEndPix, geneYLocation + self.EACH_GENE_HEIGHT/2*zoom, color=outlineColor, width=1) + + #draw the arrows + for xCoord in range(0, geneEndPix-geneStartPix): + + if (xCoord % self.EACH_GENE_ARROW_SPACING == 0 and xCoord + self.EACH_GENE_ARROW_SPACING < geneEndPix-geneStartPix) or xCoord == 0: + if strand == "+": + canvas.drawLine(geneStartPix + xCoord, geneYLocation, geneStartPix + xCoord + self.EACH_GENE_ARROW_WIDTH, geneYLocation +(self.EACH_GENE_HEIGHT / 2)*zoom, color=arrowColor, width=1) + canvas.drawLine(geneStartPix + xCoord, geneYLocation + self.EACH_GENE_HEIGHT*zoom, geneStartPix + xCoord+self.EACH_GENE_ARROW_WIDTH, geneYLocation + (self.EACH_GENE_HEIGHT / 2) * zoom, color=arrowColor, width=1) + else: + canvas.drawLine(geneStartPix + xCoord + self.EACH_GENE_ARROW_WIDTH, geneYLocation, geneStartPix + xCoord, geneYLocation +(self.EACH_GENE_HEIGHT / 2)*zoom, color=arrowColor, width=1) + canvas.drawLine(geneStartPix + xCoord + self.EACH_GENE_ARROW_WIDTH, geneYLocation + self.EACH_GENE_HEIGHT*zoom, geneStartPix + xCoord, geneYLocation + (self.EACH_GENE_HEIGHT / 2)*zoom, color=arrowColor, width=1) + + #draw the blocks for the exon regions + for i in range(0, len(exonStarts)): + exonStartPix = (exonStarts[i]-startMb)*plotXScale + xLeftOffset + exonEndPix = (exonEnds[i]-startMb)*plotXScale + xLeftOffset + if (exonStartPix < xLeftOffset): + exonStartPix = xLeftOffset + if (exonEndPix < xLeftOffset): + exonEndPix = xLeftOffset + if (exonEndPix > xLeftOffset + plotWidth): + exonEndPix = xLeftOffset + plotWidth + if (exonStartPix > xLeftOffset + plotWidth): + exonStartPix = xLeftOffset + plotWidth + canvas.drawRect(exonStartPix, geneYLocation, exonEndPix, (geneYLocation + self.EACH_GENE_HEIGHT*zoom), edgeColor = outlineColor, fillColor = fillColor) + + #draw gray blocks for 3' and 5' UTR blocks + if cdsStart and cdsEnd: + + utrStartPix = (txStart-startMb)*plotXScale + xLeftOffset + utrEndPix = (cdsStart-startMb)*plotXScale + xLeftOffset + if (utrStartPix < xLeftOffset): + utrStartPix = xLeftOffset + if (utrEndPix < xLeftOffset): + utrEndPix = xLeftOffset + if (utrEndPix > xLeftOffset + plotWidth): + utrEndPix = xLeftOffset + plotWidth + if (utrStartPix > xLeftOffset + plotWidth): + utrStartPix = xLeftOffset + plotWidth + canvas.drawRect(utrStartPix, geneYLocation, utrEndPix, (geneYLocation+self.EACH_GENE_HEIGHT*zoom), edgeColor=utrColor, fillColor =utrColor) + + if self.DRAW_UTR_LABELS and self.endMb - self.startMb <= self.DRAW_UTR_LABELS_MB: + if strand == "-": + labelText = "3'" + else: + labelText = "5'" + canvas.drawString(labelText, utrStartPix-9, geneYLocation+self.EACH_GENE_HEIGHT, pid.Font(face="helvetica", size=2)) + + #the second UTR region + + utrStartPix = (cdsEnd-startMb)*plotXScale + xLeftOffset + utrEndPix = (txEnd-startMb)*plotXScale + xLeftOffset + if (utrStartPix < xLeftOffset): + utrStartPix = xLeftOffset + if (utrEndPix < xLeftOffset): + utrEndPix = xLeftOffset + if (utrEndPix > xLeftOffset + plotWidth): + utrEndPix = xLeftOffset + plotWidth + if (utrStartPix > xLeftOffset + plotWidth): + utrStartPix = xLeftOffset + plotWidth + canvas.drawRect(utrStartPix, geneYLocation, utrEndPix, (geneYLocation+self.EACH_GENE_HEIGHT*zoom), edgeColor=utrColor, fillColor =utrColor) + + if self.DRAW_UTR_LABELS and self.endMb - self.startMb <= self.DRAW_UTR_LABELS_MB: + if tstrand == "-": + labelText = "5'" + else: + labelText = "3'" + canvas.drawString(labelText, utrEndPix+2, geneYLocation+self.EACH_GENE_HEIGHT, pid.Font(face="helvetica", size=2)) + + #draw the genes as rectangles + else: + canvas.drawRect(geneStartPix, geneYLocation, geneEndPix, (geneYLocation + self.EACH_GENE_HEIGHT*zoom), edgeColor = outlineColor, fillColor = fillColor) + + COORDS = "%d, %d, %d, %d" %(geneStartPix, geneYLocation, geneEndPix, (geneYLocation + self.EACH_GENE_HEIGHT)) + # NL: 06-02-2011 Rob required to display NCBI info in a new window + gifmap.areas.append(HT.Area(shape='rect',coords=COORDS,href=HREF, title=TITLE,target="_blank")) + +## BEGIN HaplotypeAnalyst + def drawHaplotypeBand(self, canvas, gifmap, plotXScale, offset= (40, 120, 80, 10), zoom = 1, startMb = None, endMb = None): + if self.plotScale != 'physic' or self.selectedChr == -1 or not self.geneCol: + return + + + fpText = open(os.path.join(webqtlConfig.TMPDIR, "hallo") + '.txt','wb') + + clickableRegionLabelFont=pid.Font(ttf="verdana", size=9, bold=0) + + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yZero = canvas.size[1] - yBottomOffset + fontZoom = zoom + widthMultiplier = 1 + + yPaddingTop = yTopOffset + + exprdrawn = 0 + + thisTrait = self.traitList[0] + _strains, _vals, _vars = thisTrait.exportInformative() + + smd=[] + for ii, _val in enumerate(_vals): + temp = GeneralObject(name=_strains[ii], value=_val) + smd.append(temp) + + smd.sort(lambda A, B: cmp(A.value, B.value)) + smd.reverse() + + bxdlist=list(self.genotype.prgy) + + oldgeneEndPix = -1 + #Initializing plotRight, error before + plotRight = xRightOffset + +#### find out PlotRight + for i, _locus in enumerate(self.genotype[0]): + txStart = self.genotype[0][i].Mb + txEnd = self.genotype[0][i].Mb + + geneStartPix = xLeftOffset + plotXScale*(float(txStart) - startMb) - 0 + geneEndPix = xLeftOffset + plotXScale*(float(txEnd) - startMb) - 0 + + drawit = 1 + if (geneStartPix < xLeftOffset): + drawit = 0; + if (geneStartPix > xLeftOffset + plotWidth): + drawit = 0; + + if drawit == 1: + + if self.genotype[0][i].name != " - " : + + plotRight = geneEndPix + 4 + + + +#### end find out PlotRight + + firstGene = 1 + lastGene = 0 + + #Sets the length to the length of the strain list. Beforehand, "oldgeno = self.genotype[0][i].genotype" + #was the only place it was initialized, which worked as long as the very start (startMb = None/0) wasn't being mapped. + #Now there should always be some value set for "oldgeno" - Zach 12/14/2010 + oldgeno = [None]*len(self.strainlist) + + for i, _locus in enumerate(self.genotype[0]): + txStart = self.genotype[0][i].Mb + txEnd = self.genotype[0][i].Mb + + geneStartPix = xLeftOffset + plotXScale*(float(txStart) - startMb) - 0 + geneEndPix = xLeftOffset + plotXScale*(float(txEnd) - startMb) + 0 + + if oldgeneEndPix >= xLeftOffset: + drawStart = oldgeneEndPix + 4 + else: + drawStart = xLeftOffset + 3 + + drawEnd = plotRight - 9 + + drawit = 1 + + if (geneStartPix < xLeftOffset): + if firstGene == 1: + drawit = 1 + else: + drawit = 0 + + elif (geneStartPix > (xLeftOffset + plotWidth - 3)): + if lastGene == 0: + drawit = 1 + drawEnd = xLeftOffset + plotWidth - 6 + lastGene = 1 + else: + break + + else: + firstGene = 0 + drawit = 1 + + if drawit == 1: + myColor = pid.darkblue + outlineColor = myColor + fillColor = myColor + + maxind=0 + + #Draw Genes + + geneYLocation = yPaddingTop + self.NUM_GENE_ROWS * (self.EACH_GENE_HEIGHT)*zoom + + if 1:#drawClickableRegions: + geneYLocation += self.UCSC_BAND_HEIGHT + self.BAND_SPACING + self.ENSEMBL_BAND_HEIGHT + self.BAND_SPACING + self.WEBQTL_BAND_HEIGHT + self.BAND_SPACING + else: + geneYLocation += self.BAND_SPACING + + if self.genotype[0][i].name != " - " : + + if (firstGene == 1) and (lastGene != 1): + oldgeneEndPix = drawStart = xLeftOffset + oldgeno = self.genotype[0][i].genotype + continue + + for j,_geno in enumerate (self.genotype[0][i].genotype): + + plotbxd=0 + for item in smd: + if item.name == bxdlist[j]: + plotbxd=1 + + if (plotbxd == 1): + ind = 0 + counter = 0 + for item in smd: + counter = counter + 1 + if item.name == bxdlist[j]: + ind = counter + maxind=max(ind,maxind) + + # lines + if (oldgeno[j] == -1 and _geno == -1): + mylineColor = self.HAPLOTYPE_NEGATIVE + elif (oldgeno[j] == 1 and _geno == 1): + mylineColor = self.HAPLOTYPE_POSITIVE + elif (oldgeno[j] == 0 and _geno == 0): + mylineColor = self.HAPLOTYPE_HETEROZYGOUS + else: + mylineColor = self.HAPLOTYPE_RECOMBINATION # XZ: Unknown + + canvas.drawLine(drawStart, geneYLocation+7+2*ind*self.EACH_GENE_HEIGHT*zoom, drawEnd, geneYLocation+7+2*ind*self.EACH_GENE_HEIGHT*zoom, color = mylineColor, width=zoom*(self.EACH_GENE_HEIGHT+2)) + + fillColor=pid.black + outlineColor=pid.black + if lastGene == 0: + canvas.drawRect(geneStartPix, geneYLocation+2*ind*self.EACH_GENE_HEIGHT*zoom, geneEndPix, geneYLocation+2*ind*self.EACH_GENE_HEIGHT+ 2*self.EACH_GENE_HEIGHT*zoom, edgeColor = outlineColor, fillColor = fillColor) + + + COORDS = "%d, %d, %d, %d" %(geneStartPix, geneYLocation+ind*self.EACH_GENE_HEIGHT, geneEndPix+1, (geneYLocation + ind*self.EACH_GENE_HEIGHT)) + TITLE = "Strain: %s, marker (%s) \n Position %2.3f Mb." % (bxdlist[j], self.genotype[0][i].name, float(txStart)) + HREF = '' + gifmap.areas.append(HT.Area(shape='rect',coords=COORDS,href=HREF, title=TITLE)) + + # if there are no more markers in a chromosome, the plotRight value calculated above will be before the plotWidth + # resulting in some empty space on the right side of the plot area. This draws an "unknown" bar from plotRight to the edge. + if (plotRight < (xLeftOffset + plotWidth - 3)) and (lastGene == 0): + drawEnd = xLeftOffset + plotWidth - 6 + mylineColor = self.HAPLOTYPE_RECOMBINATION + canvas.drawLine(plotRight, geneYLocation+7+2*ind*self.EACH_GENE_HEIGHT*zoom, drawEnd, geneYLocation+7+2*ind*self.EACH_GENE_HEIGHT*zoom, color = mylineColor, width=zoom*(self.EACH_GENE_HEIGHT+2)) + + + if lastGene == 0: + canvas.drawString("%s" % (self.genotype[0][i].name), geneStartPix , geneYLocation+17+2*maxind*self.EACH_GENE_HEIGHT*zoom, font=pid.Font(ttf="verdana", size=12, bold=0), color=pid.black, angle=-90) + + oldgeneEndPix = geneEndPix; + oldgeno = self.genotype[0][i].genotype + firstGene = 0 + else: + lastGene = 0 + + for j,_geno in enumerate (self.genotype[0][1].genotype): + + plotbxd=0 + for item in smd: + if item.name == bxdlist[j]: + plotbxd=1 + + if (plotbxd == 1): + + ind = 0 + counter = 0 + expr = 0 + for item in smd: + counter = counter + 1 + if item.name == bxdlist[j]: + ind = counter + expr = item.value + + # Place where font is hardcoded + canvas.drawString("%s" % (bxdlist[j]), (xLeftOffset + plotWidth + 10) , geneYLocation+8+2*ind*self.EACH_GENE_HEIGHT*zoom, font=pid.Font(ttf="verdana", size=12, bold=0), color=pid.black) + canvas.drawString("%2.2f" % (expr), (xLeftOffset + plotWidth + 60) , geneYLocation+8+2*ind*self.EACH_GENE_HEIGHT*zoom, font=pid.Font(ttf="verdana", size=12, bold=0), color=pid.black) + + fpText.close() + +## END HaplotypeAnalyst + + def drawClickBand(self, canvas, gifmap, plotXScale, offset= (40, 120, 80, 10), zoom = 1, startMb = None, endMb = None): + if self.plotScale != 'physic' or self.selectedChr == -1: + return + + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yZero = canvas.size[1] - yBottomOffset + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + + # only draw this many clickable regions (if you set it higher, you get more precision in clicking, + # but it makes the HTML huge, and takes forever to render the page in the first place) + # Draw the bands that you can click on to go to UCSC / Ensembl + MAX_CLICKABLE_REGION_DIVISIONS = 100 + clickableRegionLabelFont=pid.Font(ttf="verdana", size=9, bold=0) + pixelStep = max(5, int(float(plotWidth)/MAX_CLICKABLE_REGION_DIVISIONS)) + # pixelStep: every N pixels, we make a new clickable area for the user to go to that area of the genome. + + numBasesCurrentlyOnScreen = self.kONE_MILLION*abs(startMb - endMb) # Number of bases on screen now + flankingWidthInBases = int ( min( (float(numBasesCurrentlyOnScreen) / 2.0), (5*self.kONE_MILLION) ) ) + webqtlZoomWidth = numBasesCurrentlyOnScreen / 16.0 + # Flanking width should be such that we either zoom in to a 10 million base region, or we show the clicked region at the same scale as we are currently seeing. + + currentChromosome = self.genotype[0].name + i = 0 + + paddingTop = yTopOffset + ucscPaddingTop = paddingTop + self.WEBQTL_BAND_HEIGHT + self.BAND_SPACING + ensemblPaddingTop = ucscPaddingTop + self.UCSC_BAND_HEIGHT + self.BAND_SPACING + + if zoom == 1: + for pixel in range(xLeftOffset, xLeftOffset + plotWidth, pixelStep): + + calBase = self.kONE_MILLION*(startMb + (endMb-startMb)*(pixel-xLeftOffset-0.0)/plotWidth) + + xBrowse1 = pixel + xBrowse2 = min(xLeftOffset + plotWidth, (pixel + pixelStep - 1)) + + WEBQTL_COORDS = "%d, %d, %d, %d" % (xBrowse1, paddingTop, xBrowse2, (paddingTop+self.WEBQTL_BAND_HEIGHT)) + bandWidth = xBrowse2 - xBrowse1 + WEBQTL_HREF = "javascript:centerIntervalMapOnRange2('%s', %f, %f, document.changeViewForm)" % (currentChromosome, max(0, (calBase-webqtlZoomWidth))/1000000.0, (calBase+webqtlZoomWidth)/1000000.0) + + WEBQTL_TITLE = "Click to view this section of the genome in WebQTL" + gifmap.areas.append(HT.Area(shape='rect',coords=WEBQTL_COORDS,href=WEBQTL_HREF, title=WEBQTL_TITLE)) + canvas.drawRect(xBrowse1, paddingTop, xBrowse2, (paddingTop + self.WEBQTL_BAND_HEIGHT), edgeColor=self.CLICKABLE_WEBQTL_REGION_COLOR, fillColor=self.CLICKABLE_WEBQTL_REGION_COLOR) + canvas.drawLine(xBrowse1, paddingTop, xBrowse1, (paddingTop + self.WEBQTL_BAND_HEIGHT), color=self.CLICKABLE_WEBQTL_REGION_OUTLINE_COLOR) + + UCSC_COORDS = "%d, %d, %d, %d" %(xBrowse1, ucscPaddingTop, xBrowse2, (ucscPaddingTop+self.UCSC_BAND_HEIGHT)) + if self.species == "mouse": + UCSC_HREF = "http://genome.ucsc.edu/cgi-bin/hgTracks?db=%s&position=chr%s:%d-%d&hgt.customText=%s/snp/chr%s" % (self._ucscDb, currentChromosome, max(0, calBase-flankingWidthInBases), calBase+flankingWidthInBases, webqtlConfig.PORTADDR, currentChromosome) + else: + UCSC_HREF = "http://genome.ucsc.edu/cgi-bin/hgTracks?db=%s&position=chr%s:%d-%d" % (self._ucscDb, currentChromosome, max(0, calBase-flankingWidthInBases), calBase+flankingWidthInBases) + UCSC_TITLE = "Click to view this section of the genome in the UCSC Genome Browser" + gifmap.areas.append(HT.Area(shape='rect',coords=UCSC_COORDS,href=UCSC_HREF, title=UCSC_TITLE)) + canvas.drawRect(xBrowse1, ucscPaddingTop, xBrowse2, (ucscPaddingTop+self.UCSC_BAND_HEIGHT), edgeColor=self.CLICKABLE_UCSC_REGION_COLOR, fillColor=self.CLICKABLE_UCSC_REGION_COLOR) + canvas.drawLine(xBrowse1, ucscPaddingTop, xBrowse1, (ucscPaddingTop+self.UCSC_BAND_HEIGHT), color=self.CLICKABLE_UCSC_REGION_OUTLINE_COLOR) + + ENSEMBL_COORDS = "%d, %d, %d, %d" %(xBrowse1, ensemblPaddingTop, xBrowse2, (ensemblPaddingTop+self.ENSEMBL_BAND_HEIGHT)) + if self.species == "mouse": + ENSEMBL_HREF = "http://www.ensembl.org/Mus_musculus/contigview?highlight=&chr=%s&vc_start=%d&vc_end=%d&x=35&y=12" % (currentChromosome, max(0, calBase-flankingWidthInBases), calBase+flankingWidthInBases) + else: + ENSEMBL_HREF = "http://www.ensembl.org/Rattus_norvegicus/contigview?chr=%s&start=%d&end=%d" % (currentChromosome, max(0, calBase-flankingWidthInBases), calBase+flankingWidthInBases) + ENSEMBL_TITLE = "Click to view this section of the genome in the Ensembl Genome Browser" + gifmap.areas.append(HT.Area(shape='rect',coords=ENSEMBL_COORDS,href=ENSEMBL_HREF, title=ENSEMBL_TITLE)) + canvas.drawRect(xBrowse1, ensemblPaddingTop, xBrowse2, (ensemblPaddingTop+self.ENSEMBL_BAND_HEIGHT), edgeColor=self.CLICKABLE_ENSEMBL_REGION_COLOR, fillColor=self.CLICKABLE_ENSEMBL_REGION_COLOR) + canvas.drawLine(xBrowse1, ensemblPaddingTop, xBrowse1, (ensemblPaddingTop+self.ENSEMBL_BAND_HEIGHT), color=self.CLICKABLE_ENSEMBL_REGION_OUTLINE_COLOR) + # end for + + canvas.drawString("Click to view the corresponding section of the genome in an 8x expanded WebQTL map", (xLeftOffset + 10), paddingTop + self.WEBQTL_BAND_HEIGHT/2, font=clickableRegionLabelFont, color=self.CLICKABLE_WEBQTL_TEXT_COLOR) + canvas.drawString("Click to view the corresponding section of the genome in the UCSC Genome Browser", (xLeftOffset + 10), ucscPaddingTop + self.UCSC_BAND_HEIGHT/2, font=clickableRegionLabelFont, color=self.CLICKABLE_UCSC_TEXT_COLOR) + canvas.drawString("Click to view the corresponding section of the genome in the Ensembl Genome Browser", (xLeftOffset+10), ensemblPaddingTop + self.ENSEMBL_BAND_HEIGHT/2, font=clickableRegionLabelFont, color=self.CLICKABLE_ENSEMBL_TEXT_COLOR) + + #draw the gray text + chrFont = pid.Font(ttf="verdana", size=26*zoom, bold=1) + traitFont = pid.Font(ttf="verdana", size=14, bold=0) + chrX = xLeftOffset + plotWidth - 2 - canvas.stringWidth("Chr %s" % currentChromosome, font=chrFont) + canvas.drawString("Chr %s" % currentChromosome, chrX, ensemblPaddingTop-5, font=chrFont, color=pid.gray) + traitX = chrX - 28 - canvas.stringWidth("database", font=traitFont) + # end of drawBrowserClickableRegions + else: + #draw the gray text + chrFont = pid.Font(ttf="verdana", size=26*zoom, bold=1) + traitFont = pid.Font(ttf="verdana", size=14, bold=0) + chrX = xLeftOffset + (plotWidth - canvas.stringWidth("Chr %s" % currentChromosome, font=chrFont))/2 + canvas.drawString("Chr %s" % currentChromosome, chrX, 32, font=chrFont, color=pid.gray) + traitX = chrX - 28 - canvas.stringWidth("database", font=traitFont) + # end of drawBrowserClickableRegions + pass + + def drawXAxis(self, canvas, drawAreaHeight, gifmap, plotXScale, showLocusForm, offset= (40, 120, 80, 10), zoom = 1, startMb = None, endMb = None): + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yZero = canvas.size[1] - yBottomOffset + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + + #Parameters + NUM_MINOR_TICKS = 5 # Number of minor ticks between major ticks + X_MAJOR_TICK_THICKNESS = 2 + X_MINOR_TICK_THICKNESS = 1 + X_AXIS_THICKNESS = 1*zoom + + # ======= Alex: Draw the X-axis labels (megabase location) + MBLabelFont = pid.Font(ttf="verdana", size=15*zoom, bold=0) + xMajorTickHeight = 10 * zoom # How high the tick extends below the axis + xMinorTickHeight = 5*zoom + xAxisTickMarkColor = pid.black + xAxisLabelColor = pid.black + fontHeight = 12*fontZoom # How tall the font that we're using is + spacingFromLabelToAxis = 5 + spacingFromLineToLabel = 3 + + if self.plotScale == 'physic': + strYLoc = yZero + spacingFromLabelToAxis + canvas.fontHeight(MBLabelFont) + ###Physical single chromosome view + if self.selectedChr > -1: + graphMbWidth = endMb - startMb + XScale = Plot.detScale(startMb, endMb) + XStart, XEnd, XStep = XScale + if XStep < 8: + XStep *= 2 + spacingAmtX = spacingAmt = (XEnd-XStart)/XStep + + j = 0 + while abs(spacingAmtX -int(spacingAmtX)) >= spacingAmtX/100.0 and j < 6: + j += 1 + spacingAmtX *= 10 + + formatStr = '%%2.%df' % j + + for counter, _Mb in enumerate(Plot.frange(XStart, XEnd, spacingAmt / NUM_MINOR_TICKS)): + if _Mb < startMb or _Mb > endMb: + continue + Xc = xLeftOffset + plotXScale*(_Mb - startMb) + if counter % NUM_MINOR_TICKS == 0: # Draw a MAJOR mark, not just a minor tick mark + canvas.drawLine(Xc, yZero, Xc, yZero+xMajorTickHeight, color=xAxisTickMarkColor, width=X_MAJOR_TICK_THICKNESS) # Draw the MAJOR tick mark + labelStr = str(formatStr % _Mb) # What Mbase location to put on the label + strWidth = canvas.stringWidth(labelStr, font=MBLabelFont) + drawStringXc = (Xc - (strWidth / 2.0)) + canvas.drawString(labelStr, drawStringXc, strYLoc, font=MBLabelFont, color=xAxisLabelColor, angle=0) + else: + canvas.drawLine(Xc, yZero, Xc, yZero+xMinorTickHeight, color=xAxisTickMarkColor, width=X_MINOR_TICK_THICKNESS) # Draw the MINOR tick mark + # end else + + ###Physical genome wide view + else: + distScale = 0 + startPosX = xLeftOffset + for i, distLen in enumerate(self.ChrLengthDistList): + if distScale == 0: #universal scale in whole genome mapping + if distLen > 75: + distScale = 25 + elif distLen > 30: + distScale = 10 + else: + distScale = 5 + for tickdists in range(distScale, ceil(distLen), distScale): + canvas.drawLine(startPosX + tickdists*plotXScale, yZero, startPosX + tickdists*plotXScale, yZero + 7, color=pid.black, width=1*zoom) + canvas.drawString(str(tickdists), startPosX+tickdists*plotXScale, yZero + 10*zoom, color=pid.black, font=MBLabelFont, angle=270) + startPosX += (self.ChrLengthDistList[i]+self.GraphInterval)*plotXScale + + megabaseLabelFont = pid.Font(ttf="verdana", size=18*zoom*1.5, bold=0) + canvas.drawString("Megabases", xLeftOffset + (plotWidth - canvas.stringWidth("Megabases", font=megabaseLabelFont))/2, + strYLoc + canvas.fontHeight(MBLabelFont)+ 10*(zoom%2) + 10, font=megabaseLabelFont, color=pid.black) + pass + else: + ChrAInfo = [] + preLpos = -1 + distinctCount = 0.0 + if len(self.genotype) > 1: + for i, _chr in enumerate(self.genotype): + thisChr = [] + Locus0CM = _chr[0].cM + nLoci = len(_chr) + if nLoci <= 8: + for _locus in _chr: + if _locus.name != ' - ': + if _locus.cM != preLpos: + distinctCount += 1 + preLpos = _locus.cM + thisChr.append([_locus.name, _locus.cM-Locus0CM]) + else: + for j in (0, nLoci/4, nLoci/2, nLoci*3/4, -1): + while _chr[j].name == ' - ': + j += 1 + if _chr[j].cM != preLpos: + distinctCount += 1 + preLpos = _chr[j].cM + thisChr.append([_chr[j].name, _chr[j].cM-Locus0CM]) + ChrAInfo.append(thisChr) + else: + for i, _chr in enumerate(self.genotype): + thisChr = [] + Locus0CM = _chr[0].cM + for _locus in _chr: + if _locus.name != ' - ': + if _locus.cM != preLpos: + distinctCount += 1 + preLpos = _locus.cM + thisChr.append([_locus.name, _locus.cM-Locus0CM]) + ChrAInfo.append(thisChr) + + stepA = (plotWidth+0.0)/distinctCount + + LRectWidth = 10 + LRectHeight = 3 + offsetA = -stepA + lineColor = pid.lightblue + startPosX = xLeftOffset + for j, ChrInfo in enumerate(ChrAInfo): + preLpos = -1 + for i, item in enumerate(ChrInfo): + Lname,Lpos = item + if Lpos != preLpos: + offsetA += stepA + differ = 1 + else: + differ = 0 + preLpos = Lpos + Lpos *= plotXScale + if self.selectedChr > -1: + Zorder = i % 5 + else: + Zorder = 0 + if differ: + canvas.drawLine(startPosX+Lpos,yZero,xLeftOffset+offsetA,\ + yZero+25, color=lineColor) + canvas.drawLine(xLeftOffset+offsetA,yZero+25,xLeftOffset+offsetA,\ + yZero+40+Zorder*(LRectWidth+3),color=lineColor) + rectColor = pid.orange + else: + canvas.drawLine(xLeftOffset+offsetA, yZero+40+Zorder*(LRectWidth+3)-3,\ + xLeftOffset+offsetA, yZero+40+Zorder*(LRectWidth+3),color=lineColor) + rectColor = pid.deeppink + canvas.drawRect(xLeftOffset+offsetA, yZero+40+Zorder*(LRectWidth+3),\ + xLeftOffset+offsetA-LRectHeight,yZero+40+Zorder*(LRectWidth+3)+LRectWidth,\ + edgeColor=rectColor,fillColor=rectColor,edgeWidth = 0) + COORDS="%d,%d,%d,%d"%(xLeftOffset+offsetA-LRectHeight, yZero+40+Zorder*(LRectWidth+3),\ + xLeftOffset+offsetA,yZero+40+Zorder*(LRectWidth+3)+LRectWidth) + HREF="javascript:showDatabase3('%s','%s','%s','');" % (showLocusForm,fd.RISet+"Geno", Lname) + Areas=HT.Area(shape='rect',coords=COORDS,href=HREF, title="Locus : " + Lname) + gifmap.areas.append(Areas) + ##piddle bug + if j == 0: + canvas.drawLine(startPosX,yZero,startPosX,yZero+40, color=lineColor) + startPosX += (self.ChrLengthDistList[j]+self.GraphInterval)*plotXScale + + canvas.drawLine(xLeftOffset, yZero, xLeftOffset+plotWidth, yZero, color=pid.black, width=X_AXIS_THICKNESS) # Draw the X axis itself + + + def drawQTL(self, canvas, drawAreaHeight, gifmap, plotXScale, offset= (40, 120, 80, 10), zoom = 1, startMb = None, endMb = None): + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + + INTERCROSS = (self.genotype.type=="intercross") + + LRSHeightThresh = drawAreaHeight + AdditiveHeightThresh = drawAreaHeight/2 + DominanceHeightThresh = drawAreaHeight/2 + + #draw the LRS scale + #We first determine whether or not we are using a sliding scale. + #If so, we need to compute the maximum LRS value to determine where the max y-value should be, and call this LRSMax. + #LRSTop is then defined to be above the LRSMax by enough to add one additional LRSScale increment. + #if we are using a set-scale, then we set LRSTop to be the user's value, and LRSMax doesn't matter. + + if self.LRS_LOD == 'LOD': + lodm = self.LODFACTOR + else: + lodm = 1.0 + + if self.lrsMax <= 0: #sliding scale + LRSMax = max(map(max, self.qtlresults)).lrs + #genotype trait will give infinite LRS + LRSMax = min(LRSMax, webqtlConfig.MAXLRS) + if self.permChecked and not self.multipleInterval: + self.significance = min(self.significance, webqtlConfig.MAXLRS) + self.suggestive = min(self.suggestive, webqtlConfig.MAXLRS) + LRSMax = max(self.significance, LRSMax) + else: + LRSMax = self.lrsMax*lodm + + if LRSMax/lodm > 100: + LRSScale = 20.0 + elif LRSMax/lodm > 20: + LRSScale = 5.0 + elif LRSMax/lodm > 7.5: + LRSScale = 2.5 + else: + LRSScale = 1.0 + + LRSAxisList = Plot.frange(LRSScale, LRSMax/lodm, LRSScale) + #make sure the user's value appears on the y-axis + #update by NL 6-21-2011: round the LOD value to 100 when LRSMax is equal to 460 + LRSAxisList.append(round(LRSMax/lodm)) + + #draw the "LRS" or "LOD" string to the left of the axis + LRSScaleFont=pid.Font(ttf="verdana", size=16*zoom, bold=0) + LRSLODFont=pid.Font(ttf="verdana", size=18*zoom*1.5, bold=0) + yZero = yTopOffset + plotHeight + + canvas.drawString(self.LRS_LOD, xLeftOffset - canvas.stringWidth("999.99", font=LRSScaleFont) - 15*(zoom-1), \ + yZero - 150 - 300*(zoom - 1), font=LRSLODFont, color=pid.black, angle=90) + + for item in LRSAxisList: + if LRSMax == 0.0: + LRSMax = 0.000001 + yLRS = yZero - (item*lodm/LRSMax) * LRSHeightThresh + canvas.drawLine(xLeftOffset, yLRS, xLeftOffset - 4, yLRS, color=self.LRS_COLOR, width=1*zoom) + scaleStr = "%2.1f" % item + #Draw the LRS/LOD Y axis label + canvas.drawString(scaleStr, xLeftOffset-4-canvas.stringWidth(scaleStr, font=LRSScaleFont)-5, yLRS+3, font=LRSScaleFont, color=self.LRS_COLOR) + + + #"Significant" and "Suggestive" Drawing Routine + # ======= Draw the thick lines for "Significant" and "Suggestive" ===== (crowell: I tried to make the SNPs draw over these lines, but piddle wouldn't have it...) + if self.permChecked and not self.multipleInterval: + significantY = yZero - self.significance*LRSHeightThresh/LRSMax + suggestiveY = yZero - self.suggestive*LRSHeightThresh/LRSMax + startPosX = xLeftOffset + for i, _chr in enumerate(self.genotype): + rightEdge = int(startPosX + self.ChrLengthDistList[i]*plotXScale - self.SUGGESTIVE_WIDTH/1.5) + canvas.drawLine(startPosX+self.SUGGESTIVE_WIDTH/1.5, suggestiveY, rightEdge, suggestiveY, color=self.SUGGESTIVE_COLOR, + width=self.SUGGESTIVE_WIDTH*zoom, clipX=(xLeftOffset, xLeftOffset + plotWidth-2)) + canvas.drawLine(startPosX+self.SUGGESTIVE_WIDTH/1.5, significantY, rightEdge, significantY, color=self.SIGNIFICANT_COLOR, + width=self.SIGNIFICANT_WIDTH*zoom, clipX=(xLeftOffset, xLeftOffset + plotWidth-2)) + sugg_coords = "%d, %d, %d, %d" % (startPosX, suggestiveY-2, rightEdge + 2*zoom, suggestiveY+2) + sig_coords = "%d, %d, %d, %d" % (startPosX, significantY-2, rightEdge + 2*zoom, significantY+2) + if self.LRS_LOD == 'LRS': + sugg_title = "Suggestive LRS = %0.2f" % self.suggestive + sig_title = "Significant LRS = %0.2f" % self.significance + else: + sugg_title = "Suggestive LOD = %0.2f" % (self.suggestive/4.61) + sig_title = "Significant LOD = %0.2f" % (self.significance/4.61) + Areas1 = HT.Area(shape='rect',coords=sugg_coords,title=sugg_title) + Areas2 = HT.Area(shape='rect',coords=sig_coords,title=sig_title) + gifmap.areas.append(Areas1) + gifmap.areas.append(Areas2) + + startPosX += (self.ChrLengthDistList[i]+self.GraphInterval)*plotXScale + + + if self.multipleInterval: + lrsEdgeWidth = 1 + else: + additiveMax = max(map(lambda X : abs(X.additive), self.qtlresults[0])) + if INTERCROSS: + dominanceMax = max(map(lambda X : abs(X.dominance), self.qtlresults[0])) + else: + dominanceMax = -1 + lrsEdgeWidth = 2 + + if zoom == 2: + lrsEdgeWidth = 2 * lrsEdgeWidth + for i, qtlresult in enumerate(self.qtlresults): + m = 0 + startPosX = xLeftOffset + thisLRSColor = self.colorCollection[i] + for j, _chr in enumerate(self.genotype): + LRSCoordXY = [] + AdditiveCoordXY = [] + DominanceCoordXY = [] + for k, _locus in enumerate(_chr): + if self.plotScale == 'physic': + Xc = startPosX + (_locus.Mb-startMb)*plotXScale + else: + Xc = startPosX + (_locus.cM-_chr[0].cM)*plotXScale + # updated by NL 06-18-2011: + # fix the over limit LRS graph issue since genotype trait may give infinite LRS; + # for any lrs is over than 460(LRS max in this system), it will be reset to 460 + if qtlresult[m].lrs> 460 or qtlresult[m].lrs=='inf': + Yc = yZero - webqtlConfig.MAXLRS*LRSHeightThresh/LRSMax + else: + Yc = yZero - qtlresult[m].lrs*LRSHeightThresh/LRSMax + + LRSCoordXY.append((Xc, Yc)) + if not self.multipleInterval and self.additiveChecked: + if additiveMax == 0.0: + additiveMax = 0.000001 + Yc = yZero - qtlresult[m].additive*AdditiveHeightThresh/additiveMax + AdditiveCoordXY.append((Xc, Yc)) + if not self.multipleInterval and INTERCROSS and self.additiveChecked: + Yc = yZero - qtlresult[m].dominance*DominanceHeightThresh/dominanceMax + DominanceCoordXY.append((Xc, Yc)) + m += 1 + canvas.drawPolygon(LRSCoordXY,edgeColor=thisLRSColor,closed=0, edgeWidth=lrsEdgeWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + + lineWidth = 1 + if not self.multipleInterval and self.additiveChecked: + plusColor = self.ADDITIVE_COLOR_POSITIVE + minusColor = self.ADDITIVE_COLOR_NEGATIVE + for k, aPoint in enumerate(AdditiveCoordXY): + if k > 0: + Xc0, Yc0 = AdditiveCoordXY[k-1] + Xc, Yc = aPoint + if (Yc0-yZero)*(Yc-yZero) < 0: + if Xc == Xc0: #genotype , locus distance is 0 + Xcm = Xc + else: + Xcm = (yZero-Yc0)/((Yc-Yc0)/(Xc-Xc0)) +Xc0 + if Yc0 < yZero: + canvas.drawLine(Xc0, Yc0, Xcm, yZero, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + canvas.drawLine(Xcm, yZero, Xc, yZero-(Yc-yZero), color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + else: + canvas.drawLine(Xc0, yZero - (Yc0-yZero), Xcm, yZero, color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + canvas.drawLine(Xcm, yZero, Xc, Yc, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + elif (Yc0-yZero)*(Yc-yZero) > 0: + if Yc < yZero: + canvas.drawLine(Xc0, Yc0, Xc, Yc, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + else: + canvas.drawLine(Xc0, yZero - (Yc0-yZero), Xc, yZero - (Yc-yZero), color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + else: + minYc = min(Yc-yZero, Yc0-yZero) + if minYc < 0: + canvas.drawLine(Xc0, Yc0, Xc, Yc, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + else: + canvas.drawLine(Xc0, yZero - (Yc0-yZero), Xc, yZero - (Yc-yZero), color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + if not self.multipleInterval and INTERCROSS and self.dominanceChecked: + plusColor = self.DOMINANCE_COLOR_POSITIVE + minusColor = self.DOMINANCE_COLOR_NEGATIVE + for k, aPoint in enumerate(DominanceCoordXY): + if k > 0: + Xc0, Yc0 = DominanceCoordXY[k-1] + Xc, Yc = aPoint + if (Yc0-yZero)*(Yc-yZero) < 0: + if Xc == Xc0: #genotype , locus distance is 0 + Xcm = Xc + else: + Xcm = (yZero-Yc0)/((Yc-Yc0)/(Xc-Xc0)) +Xc0 + if Yc0 < yZero: + canvas.drawLine(Xc0, Yc0, Xcm, yZero, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + canvas.drawLine(Xcm, yZero, Xc, yZero-(Yc-yZero), color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + else: + canvas.drawLine(Xc0, yZero - (Yc0-yZero), Xcm, yZero, color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + canvas.drawLine(Xcm, yZero, Xc, Yc, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + elif (Yc0-yZero)*(Yc-yZero) > 0: + if Yc < yZero: + canvas.drawLine(Xc0, Yc0, Xc, Yc, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + else: + canvas.drawLine(Xc0, yZero - (Yc0-yZero), Xc, yZero - (Yc-yZero), color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + else: + minYc = min(Yc-yZero, Yc0-yZero) + if minYc < 0: + canvas.drawLine(Xc0, Yc0, Xc, Yc, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + else: + canvas.drawLine(Xc0, yZero - (Yc0-yZero), Xc, yZero - (Yc-yZero), color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + startPosX += (self.ChrLengthDistList[j]+self.GraphInterval)*plotXScale + + ###draw additive scale + if not self.multipleInterval and self.additiveChecked: + additiveScaleFont=pid.Font(ttf="verdana",size=16*zoom,bold=0) + additiveScale = Plot.detScaleOld(0,additiveMax) + additiveStep = (additiveScale[1]-additiveScale[0])/additiveScale[2] + additiveAxisList = Plot.frange(0, additiveScale[1], additiveStep) + maxAdd = additiveScale[1] + addPlotScale = AdditiveHeightThresh/additiveMax + + additiveAxisList.append(additiveScale[1]) + for item in additiveAxisList: + additiveY = yZero - item*addPlotScale + canvas.drawLine(xLeftOffset + plotWidth,additiveY,xLeftOffset+4+ plotWidth,additiveY,color=self.ADDITIVE_COLOR_POSITIVE, width=1*zoom) + scaleStr = "%2.3f" % item + canvas.drawString(scaleStr,xLeftOffset + plotWidth +6,additiveY+5,font=additiveScaleFont,color=self.ADDITIVE_COLOR_POSITIVE) + + canvas.drawLine(xLeftOffset+plotWidth,additiveY,xLeftOffset+plotWidth,yZero,color=self.ADDITIVE_COLOR_POSITIVE, width=1*zoom) + + canvas.drawLine(xLeftOffset, yZero, xLeftOffset, yTopOffset + 30*(zoom - 1), color=self.LRS_COLOR, width=1*zoom) #the blue line running up the y axis + + + def drawGraphBackground(self, canvas, gifmap, offset= (80, 120, 80, 50), zoom = 1, startMb = None, endMb = None): + ##conditions + ##multiple Chromosome view + ##single Chromosome Physical + ##single Chromosome Genetic + xLeftOffset, xRightOffset, yTopOffset, yBottomOffset = offset + plotWidth = canvas.size[0] - xLeftOffset - xRightOffset + plotHeight = canvas.size[1] - yTopOffset - yBottomOffset + yBottom = yTopOffset+plotHeight + fontZoom = zoom + if zoom == 2: + fontZoom = 1.5 + yTopOffset += 30 + + #calculate plot scale + if self.plotScale != 'physic': + self.ChrLengthDistList = self.ChrLengthCMList + drawRegionDistance = self.ChrLengthCMSum + else: + self.ChrLengthDistList = self.ChrLengthMbList + drawRegionDistance = self.ChrLengthMbSum + + if self.selectedChr > -1: #single chromosome view + spacingAmt = plotWidth/13.5 + i = 0 + for startPix in Plot.frange(xLeftOffset, xLeftOffset+plotWidth, spacingAmt): + if (i % 2 == 0): + theBackColor = self.GRAPH_BACK_DARK_COLOR + else: + theBackColor = self.GRAPH_BACK_LIGHT_COLOR + i += 1 + canvas.drawRect(startPix, yTopOffset, min(startPix+spacingAmt, xLeftOffset+plotWidth), \ + yBottom, edgeColor=theBackColor, fillColor=theBackColor) + + drawRegionDistance = self.ChrLengthDistList[self.selectedChr] + self.ChrLengthDistList = [drawRegionDistance] + if self.plotScale == 'physic': + plotXScale = plotWidth / (endMb-startMb) + else: + plotXScale = plotWidth / drawRegionDistance + + else: #multiple chromosome view + plotXScale = plotWidth / ((len(self.genotype)-1)*self.GraphInterval + drawRegionDistance) + + startPosX = xLeftOffset + if fontZoom == 1.5: + chrFontZoom = 2 + else: + chrFontZoom = 1 + chrLabelFont=pid.Font(ttf="verdana",size=24*chrFontZoom,bold=0) + + for i, _chr in enumerate(self.genotype): + if (i % 2 == 0): + theBackColor = self.GRAPH_BACK_DARK_COLOR + else: + theBackColor = self.GRAPH_BACK_LIGHT_COLOR + + #draw the shaded boxes and the sig/sug thick lines + canvas.drawRect(startPosX, yTopOffset, startPosX + self.ChrLengthDistList[i]*plotXScale, \ + yBottom, edgeColor=pid.gainsboro,fillColor=theBackColor) + + chrNameWidth = canvas.stringWidth(_chr.name, font=chrLabelFont) + chrStartPix = startPosX + (self.ChrLengthDistList[i]*plotXScale -chrNameWidth)/2 + chrEndPix = startPosX + (self.ChrLengthDistList[i]*plotXScale +chrNameWidth)/2 + + canvas.drawString(_chr.name, chrStartPix, yTopOffset + 20 ,font = chrLabelFont,color=pid.black) + COORDS = "%d,%d,%d,%d" %(chrStartPix, yTopOffset, chrEndPix,yTopOffset +20) + + #add by NL 09-03-2010 + HREF = "javascript placeholder" + #HREF = "javascript:changeView(%d,%s);" % (i,self.ChrLengthMbList) + Areas = HT.Area(shape='rect',coords=COORDS,href=HREF) + gifmap.areas.append(Areas) + startPosX += (self.ChrLengthDistList[i]+self.GraphInterval)*plotXScale + + return plotXScale + + def calculateAllResult(self, fd): + + weightedRegression = fd.formdata.getvalue('applyVarianceSE') + + self.genotype = self.genotype.addinterval() + resultSlice = [] + controlGeno = [] + + if self.multipleInterval: + self.suggestive = 0 + self.significance = 0 + if self.selectedChr > -1: + self.genotype.chromosome = [self.genotype[self.selectedChr]] + else: + #single interval mapping + try: + self.suggestive = float(fd.formdata.getvalue('permSuggestive')) + self.significance = float(fd.formdata.getvalue('permSignificance')) + except: + self.suggestive = None + self.significance = None + + _strains, _vals, _vars = self.traitList[0].exportInformative(weightedRegression) + + if webqtlUtil.ListNotNull(_vars): + pass + else: + weightedRegression = 0 + _strains, _vals, _vars = self.traitList[0].exportInformative() + + ##locate genotype of control Locus + if self.controlLocus: + controlGeno2 = [] + _FIND = 0 + for _chr in self.genotype: + for _locus in _chr: + if _locus.name == self.controlLocus: + controlGeno2 = _locus.genotype + _FIND = 1 + break + if _FIND: + break + if controlGeno2: + _prgy = list(self.genotype.prgy) + for _strain in _strains: + _idx = _prgy.index(_strain) + controlGeno.append(controlGeno2[_idx]) + else: + return "The control marker you selected is not in the genofile." + + if weightedRegression: + self.LRSArray = self.genotype.permutation(strains = _strains, trait = _vals, + variance = _vars, nperm=self.nperm) + else: + self.LRSArray = self.genotype.permutation(strains = _strains, trait = _vals, + nperm=self.nperm) + + if self.significance and self.suggestive: + pass + else: + if self.nperm < 100: + self.suggestive = 0 + self.significance = 0 + else: + self.suggestive = self.LRSArray[int(self.nperm*0.37-1)] + self.significance = self.LRSArray[int(self.nperm*0.95-1)] + + #calculating bootstrap + #from now on, genotype could only contain a single chromosome + #permutation need to be performed genome wide, this is not the case for bootstrap + + #due to the design of qtlreaper, composite regression need to be performed genome wide + if not self.controlLocus and self.selectedChr > -1: + self.genotype.chromosome = [self.genotype[self.selectedChr]] + elif self.selectedChr > -1: #self.controlLocus and self.selectedChr > -1 + lociPerChr = map(len, self.genotype) + resultSlice = reduce(lambda X, Y: X+Y, lociPerChr[:self.selectedChr], 0) + resultSlice = [resultSlice,resultSlice+lociPerChr[self.selectedChr]] + else: + pass + + #calculate QTL for each trait + self.qtlresults = [] + + for thisTrait in self.traitList: + _strains, _vals, _vars = thisTrait.exportInformative(weightedRegression) + if self.controlLocus: + if weightedRegression: + qtlresult = self.genotype.regression(strains = _strains, trait = _vals, + variance = _vars, control = self.controlLocus) + else: + qtlresult = self.genotype.regression(strains = _strains, trait = _vals, + control = self.controlLocus) + if resultSlice: + qtlresult = qtlresult[resultSlice[0]:resultSlice[1]] + else: + if weightedRegression: + qtlresult = self.genotype.regression(strains = _strains, trait = _vals, + variance = _vars) + else: + qtlresult = self.genotype.regression(strains = _strains, trait = _vals) + + self.qtlresults.append(qtlresult) + + if not self.multipleInterval: + if self.controlLocus and self.selectedChr > -1: + self.genotype.chromosome = [self.genotype[self.selectedChr]] + + if self.bootChecked: + if controlGeno: + self.bootResult = self.genotype.bootstrap(strains = _strains, trait = _vals, + control = controlGeno, nboot=fd.nboot) + elif weightedRegression: + self.bootResult = self.genotype.bootstrap(strains = _strains, trait = _vals, + variance = _vars, nboot=fd.nboot) + else: + self.bootResult = self.genotype.bootstrap(strains = _strains, trait = _vals, + nboot=fd.nboot) + else: + self.bootResult = [] + + def calculatePValue (self, query_LRS, permutation_LRS_array): + query_index = len(permutation_LRS_array) + for i, one_permutation_LRS in enumerate(permutation_LRS_array): + if one_permutation_LRS >= query_LRS: + query_index = i + break + try: + P_value = float(len(permutation_LRS_array) - query_index) / len(permutation_LRS_array) + except: + P_value = '' + return P_value + + def helpButton(self, anchor): + return HT.Href(self.HELP_PAGE_REF + '#%s' % anchor, self.qmarkImg, target=self.HELP_WINDOW_NAME) + + + def traitRemapTD(self, cursor, fd): + chrList = HT.Select(name="chromosomes", data=self.ChrList, selected=[self.selectedChr], + onChange="chrLength(this.form.chromosomes.value, this.form.scale.value, this.form, self.ChrLengthMbList);") + + physicOnly = HT.Span(' *', Class="cr") + + showSNPCheck = HT.Input(type='checkbox', Class='checkbox', name='showSNP', value='ON', checked=self.SNPChecked) + showSNPText = HT.Span('SNP Track ', self.helpButton("snpSeismograph"), Class="fs12 fwn") + + showGenesCheck = HT.Input(type='checkbox', Class='checkbox', name='showGenes', value='ON', checked=self.geneChecked) + showGenesText = HT.Span('Gene Track', Class="fs12 fwn") + + showIntervalAnalystCheck = HT.Input(type='checkbox', Class='checkbox', name='intervalAnalystCheck', value='ON', checked=self.intervalAnalystChecked) + showIntervalAnalystText = HT.Span('Interval Analyst', Class="fs12 fwn") +## BEGIN HaplotypeAnalyst + + showHaplotypeAnalystCheck = HT.Input(type='checkbox', Class='checkbox', name='haplotypeAnalystCheck', value='ON', checked=self.haplotypeAnalystChecked) + showHaplotypeAnalystText = HT.Span('Haplotype Analyst', Class="fs12 fwn") +## END HaplotypeAnalyst + + leftBox = HT.Input(type="text", name="startMb", size=10) + rightBox = HT.Input(type="text", name="endMb", size=10) + if self.selectedChr > -1 and self.plotScale=='physic': + leftBox.value = self.startMb + rightBox.value = self.endMb + + scaleBox = HT.Select(name="scale", onChange="chrLength(this.form.chromosomes.value, this.form.scale.value, this.form, self.ChrLengthMbList);") + scaleBox.append(("Genetic", "morgan")) + if fd.genotype.Mbmap: + scaleBox.append(("Physical", "physic")) + scaleBox.selected.append(self.plotScale) + + permBox = HT.Input(type="checkbox", name="permCheck", value='ON', checked=self.permChecked, Class="checkbox") + permText = HT.Span("Permutation Test ", self.helpButton("Permutation"), Class="fs12 fwn") + bootBox = HT.Input(type="checkbox", name="bootCheck", value='ON', checked=self.bootChecked, Class="checkbox") + bootText = HT.Span("Bootstrap Test ", self.helpButton("bootstrap"), Class="fs12 fwn") + additiveBox = HT.Input(type="checkbox", name="additiveCheck", value='ON', checked=self.additiveChecked, Class="checkbox") + additiveText = HT.Span("Allele Effects ", self.helpButton("additive"), Class="fs12 fwn") + dominanceBox = HT.Input(type="checkbox", name="dominanceCheck", value='ON', checked=self.dominanceChecked, Class="checkbox") + dominanceText = HT.Span("Dominance Effects ", self.helpButton("Dominance"), Class="fs12 fwn") + + lrsRadio = HT.Input(type="radio", name="LRSCheck", value='LRS', checked = (self.LRS_LOD == "LRS")) + lodRadio = HT.Input(type="radio", name="LRSCheck", value='LOD', checked = (self.LRS_LOD != "LRS")) + lrsMaxBox = HT.Input(type="text", name="lrsMax", value=self.lrsMax, size=3) + widthBox = HT.Input(type="text", name="graphWidth", size=5, value=str(self.graphWidth)) + legendBox = HT.Input(type="checkbox", name="viewLegend", value='ON', checked=self.legendChecked, Class="checkbox") + legendText = HT.Span("Legend", Class="fs12 fwn") + + draw2XBox = HT.Input(type="checkbox", name="draw2X", value='ON', Class="checkbox") + draw2XText = HT.Span("2X Plot", Class="fs12 fwn") + + regraphButton = HT.Input(type="button", Class="button", onClick="javascript:databaseFunc(this.form,'showIntMap');", value="Remap") + controlsForm = HT.Form(cgi= os.path.join(webqtlConfig.CGIDIR, webqtlConfig.SCRIPTFILE), enctype="multipart/form-data", name="changeViewForm", submit=HT.Input(type='hidden')) + controlsTable = HT.TableLite(border=0) + innerControlsTable = HT.TableLite(border=0) + if self.selectedChr == -1: + minimumGraphWidth = self.MULT_GRAPH_MIN_WIDTH + else: + minimumGraphWidth = self.GRAPH_MIN_WIDTH + innerControlsTable.append( + HT.TR(HT.TD("Chr: ", Class="fs12 fwb ffl"),HT.TD(chrList, scaleBox, regraphButton)), + HT.TR(HT.TD("View: ", Class="fs12 fwb ffl"),HT.TD(leftBox, " to ", rightBox, "Mb", physicOnly, NOWRAP="on")), + HT.TR(HT.TD("Units: ", Class="fs12 fwb ffl"), HT.TD(lrsRadio, "LRS ", lodRadio, "LOD ", self.helpButton("LOD"))), + HT.TR(HT.TD(" ", Class="fs12 fwb ffl"), HT.TD(lrsMaxBox, "units on Y-axis (0 for default)", Class="fs11 fwn")), + HT.TR(HT.TD("Width: ", Class="fs12 fwb ffl"), HT.TD(widthBox, "pixels (minimum=%d)" % minimumGraphWidth, Class="fs11 fwn ")) + ) + #whether SNP + # comment this, because this will make caculation very slow. + #cursor.execute("Select Species.Id from SnpAll, Species where SnpAll.SpeciesId = Species.Id and Species.Name = %s limit 1", self.species) + #SNPorNot = cursor.fetchall() + SNPorNot = True + #Whether Gene + cursor.execute("Select Species.Id from GeneList, Species where GeneList.SpeciesId = Species.Id and Species.Name = %s limit 1", self.species) + GeneorNot = cursor.fetchall() + + if self.multipleInterval: + optionPanel = HT.TD(valign="top", NOWRAP="on") + else: + optionPanel = HT.TD(permBox, permText, HT.BR(), bootBox, bootText, HT.BR(), additiveBox, additiveText, HT.BR(), valign="top", NOWRAP="on") + #whether dominance + if self.genotype.type == 'intercross': + optionPanel.append(dominanceBox, dominanceText, HT.BR()) + if SNPorNot: + optionPanel.append(showSNPCheck, showSNPText, physicOnly, HT.BR()) + if GeneorNot: + optionPanel.append(showGenesCheck, showGenesText, physicOnly, HT.BR(), + showIntervalAnalystCheck, showIntervalAnalystText, physicOnly, HT.BR()) +## BEGIN HaplotypeAnalyst + optionPanel.append(showHaplotypeAnalystCheck, showHaplotypeAnalystText, physicOnly, HT.BR()) +## END HaplotypeAnalyst + optionPanel.append(legendBox, legendText, HT.BR(),draw2XBox, draw2XText) + controlsTable.append( + HT.TR(HT.TD(innerControlsTable, valign="top"), + HT.TD(" ", width=15), optionPanel), + HT.TR(HT.TD(physicOnly, " only apply to single chromosome physical mapping", align="Center", colspan=3, Class="fs11 fwn")) + ) + controlsForm.append(controlsTable) + + controlsForm.append(HT.Input(name="permSuggestive", value=self.suggestive, type="hidden")) + controlsForm.append(HT.Input(name="permSignificance", value=self.significance, type="hidden")) + +## BEGIN HaplotypeAnalyst #### haplotypeAnalystCheck added below +## END HaplotypeAnalyst + + for key in fd.formdata.keys(): + if key == "searchResult" and type([]) == type(fd.formdata.getvalue(key)): + controlsForm.append(HT.Input(name=key, value=string.join(fd.formdata.getvalue(key), "\t"), type="hidden")) + elif key not in ("endMb", "startMb", "chromosomes", "scale", "permCheck", "bootCheck", "additiveCheck", "dominanceCheck", + "LRSCheck", "intervalAnalystCheck", "haplotypeAnalystCheck", "lrsMax", "graphWidth", "viewLegend", 'showGenes', 'showSNP', 'draw2X', + 'permSuggestive', "permSignificance"): + controlsForm.append(HT.Input(name=key, value=fd.formdata.getvalue(key), type="hidden")) + else: + pass + + # updated by NL, move function changeView(i) to webqtl.js and change it to function changeView(i, Chr_Mb_list) + # move function chrLength(a, b, c) to webqtl.js and change it to function chrLength(a, b, c, Chr_Mb_list) + self.dict['js1'] = '' + return HT.TD(controlsForm, Class="doubleBorder", width=400) + + def traitInfoTD(self, fd): + if self.selectedChr == -1: + intMapHeading = HT.Paragraph('Map Viewer: Whole Genome', Class="title") + else: + intMapHeading = HT.Paragraph('Map Viewer: Chr %s' % self.genotype[0].name, Class="title") + + heading2 = HT.Paragraph(HT.Strong('Population: '), "%s %s" % (self.species.title(), fd.RISet) , HT.BR()) + #Trait is from an database + if self.traitList and self.traitList[0] and self.traitList[0].db: + #single trait + if len(self.traitList) == 1: + thisTrait = self.traitList[0] + trait_url = HT.Href(text=thisTrait.name, url = os.path.join(webqtlConfig.CGIDIR, webqtlConfig.SCRIPTFILE) + \ + "?FormID=showDatabase&incparentsf1=1&database=%s&ProbeSetID=%s" % (thisTrait.db.name, thisTrait.name), \ + target='_blank', Class="normalsize") + heading2.append(HT.Strong("Database: "), HT.Href(text=thisTrait.db.fullname, url = webqtlConfig.INFOPAGEHREF % thisTrait.db.name ,\ + target='_blank',Class="normalsize"),HT.BR()) + if thisTrait.db.type == 'ProbeSet': + heading2.append(HT.Strong('Trait ID: '), trait_url, HT.BR(), + HT.Strong("Gene Symbol: "), HT.Italic('%s' % thisTrait.symbol,id="green"),HT.BR()) + if thisTrait.chr and thisTrait.mb: + heading2.append(HT.Strong("Location: "), 'Chr %s @ %s Mb' % (thisTrait.chr, thisTrait.mb)) + elif thisTrait.db.type == 'Geno': + heading2.append(HT.Strong('Locus : '), trait_url, HT.BR()) + if thisTrait.chr and thisTrait.mb: + heading2.append(HT.Strong("Location: "), 'Chr %s @ %s Mb' % (thisTrait.chr, thisTrait.mb)) + elif thisTrait.db.type == 'Publish': + heading2.append(HT.Strong('Record ID: '), trait_url, HT.BR()) + else: + pass + else: + heading2.append(HT.Strong("Traits: "), "Multiple Traits") + else: + heading2.append(HT.Strong("Trait Name: "), fd.identification) + return HT.TD(intMapHeading, heading2, valign="top") + + def drawPermutationHistogram(self): + ######################################### + # Permutation Graph + ######################################### + myCanvas = pid.PILCanvas(size=(400,300)) + #plotBar(myCanvas,10,10,390,290,LRSArray,XLabel='LRS',YLabel='Frequency',title=' Histogram of Permutation Test',identification=fd.identification) + Plot.plotBar(myCanvas, self.LRSArray,XLabel='LRS',YLabel='Frequency',title=' Histogram of Permutation Test') + filename= webqtlUtil.genRandStr("Reg_") + myCanvas.save(webqtlConfig.IMGDIR+filename, format='gif') + img=HT.Image('/image/'+filename+'.gif',border=0,alt='Histogram of Permutation Test') + + + self.suggestive = self.LRSArray[int(self.nperm*0.37-1)] + self.significant = self.LRSArray[int(self.nperm*0.95-1)] + self.highlysignificant = self.LRSArray[int(self.nperm*0.99-1)] + + permutationHeading = HT.Paragraph('Histogram of Permutation Test') + permutationHeading.__setattr__("class","title") + + permutation = HT.TableLite() + permutation.append(HT.TR(HT.TD(img)), + HT.TR(HT.TD('')), + HT.TR(HT.TD('Total of %d permutations'%self.nperm))) + + return permutation + + def permutationTextFile(self): + filename= webqtlUtil.genRandStr("Reg_") + fpText = open('%s.txt' % (webqtlConfig.TMPDIR+filename), 'wb') + fpText.write('Suggestive LRS (p = 0.63) = %3.2f\n'%self.suggestive) + fpText.write('Significant LRS (p = 0.05) = %3.2f\n'%self.significant) + fpText.write('Highly Significant LRS (p = 0.01) = %3.2f\n\n'%self.highlysignificant) + fpText.write('%s Permutations\n\n' % str(len(self.LRSArray))) + LRSInfo =HT.Paragraph('    Suggestive LRS = %3.2f\n'%self.suggestive, + HT.BR(), + '    Significant LRS =%3.2f\n'%self.significant, + HT.BR(), + '    Highly Significant LRS =%3.2f\n' % self.highlysignificant) + + for lrs_value in self.LRSArray: + fpText.write(str(lrs_value) + "\n") + + textUrl = HT.Href(text = 'Download Permutation Results', url= '/tmp/'+filename+'.txt', target = "_blank", Class='fs12 fwn') + + return textUrl + + def geneTable(self, geneCol, refGene=None): + #SNPLink = 0 #Not sure what this is used for + + if self.species == 'mouse' or self.species == 'rat': + + gene_tblobj = {} + gene_tblobj["header"] = self.getGeneTableHeader(refGene=None) + gene_tblobj["body"] = self.getGeneTableBody(geneCol, refGene=None) + + sortby = self.getSortByValue() + + filename= webqtlUtil.genRandStr("Mapping_") + + objfile = open('%s.obj' % (webqtlConfig.TMPDIR+filename), 'wb') + cPickle.dump(gene_tblobj, objfile) + objfile.close() + + gene_table = webqtlUtil.genTableObj(tblobj=gene_tblobj, file=filename, sortby=sortby, tableID="sortable", addIndex="0") + + else: + gene_table = "" + + return gene_table + + def getLiteratureCorrelation(cursor,geneId1=None,geneId2=None): + if not geneId1 or not geneId2: + return None + if geneId1 == geneId2: + return 1.0 + geneId1 = str(geneId1) + geneId2 = str(geneId2) + lCorr = None + try: + query = 'SELECT Value FROM LCorrRamin3 WHERE GeneId1 = %s and GeneId2 = %s' + for x,y in [(geneId1,geneId2),(geneId2,geneId1)]: + cursor.execute(query,(x,y)) + lCorr = cursor.fetchone() + if lCorr: + lCorr = lCorr[0] + break + except: raise #lCorr = None + return lCorr + + def getGeneTableHeader(self, refGene=None): + + gene_tblobj_header = [] + + col_class = "fs14 fwb ffl b1 cw cbrb" + + if self.species == "mouse": + + if refGene: + gene_tblobj_header = [[THCell(HT.TD('Index', HT.BR(), HT.BR(), align='left', width=50, Class=col_class), text="index", idx=0), + THCell(HT.TD('Symbol', HT.BR(), HT.BR(), align='left', width=100, Class=col_class), text="symbol", idx=1), + THCell(HT.TD('Mb Start',HT.BR(),'(mm9)', align='left', width=100, Class=col_class), text="mb_start_mm9", idx=2), + THCell(HT.TD('Length (Kb)', HT.BR(), HT.BR(), align='left', width=100, Class=col_class), text="length", idx=3), + THCell(HT.TD('SNP',HT.BR(),'Count', align='left', width=47, Class=col_class), text="snp_count", idx=4), + THCell(HT.TD('SNP',HT.BR(),'Density', align='left', width=78, Class=col_class), text="snp_density", idx=5), + THCell(HT.TD('Avg',HT.BR(),'Expr', HT.BR(), HT.BR(), align='left', width=44, Class=col_class), sort=0, idx=6), + THCell(HT.TD('Human',HT.BR(),'Chr', align='left', width=60, Class=col_class), text="human_chr", idx=7), + THCell(HT.TD('Mb Start',HT.BR(),'(hg19)', align='left', width=100, Class=col_class), text="mb_start_hg19", idx=8), + THCell(HT.TD('Literature',HT.BR(),'Correlation', align='left', width=100, Class=col_class), text="lit_corr", idx=9), + THCell(HT.TD('Gene Description', HT.BR(), HT.BR(), align='left', width=290, Class=col_class), text="description", idx=10), + THCell(HT.TD('PolymiRTS',HT.BR(),'Database', HT.BR(), HT.Href(url='http://compbio.uthsc.edu/miRSNP/', text='>>', target="_blank", Class="normalsize"), + align='left', width=100, Class=col_class), sort=0, idx=11), + THCell(HT.TD('Gene Weaver', HT.BR(), 'Info Content', HT.BR(), HT.Href(url='http://geneweaver.org/', text='>>', target="_blank", Class="normalsize"), + align='left', width=110, Class=col_class), sort=0, idx=12), + ]] + else: + gene_tblobj_header = [[THCell(HT.TD('Index', HT.BR(), HT.BR(), align='left', width=50, Class=col_class), text="index", idx=0), + THCell(HT.TD('Symbol', HT.BR(), HT.BR(), align='left', width=100, Class=col_class), text="symbol", idx=1), + THCell(HT.TD('Mb Start',HT.BR(),'(mm9)', align='left', width=100, Class=col_class), text="mb_start_mm9", idx=2), + THCell(HT.TD('Length (Kb)', HT.BR(), HT.BR(), align='left', width=100, Class=col_class), text="length", idx=3), + THCell(HT.TD('SNP',HT.BR(),'Count', align='left', width=47, Class=col_class), text="snp_count", idx=4), + THCell(HT.TD('SNP',HT.BR(),'Density', align='left', width=78, Class=col_class), text="snp_density", idx=5), + THCell(HT.TD('Avg',HT.BR(),'Expr', HT.BR(), HT.BR(), align='left', width=44, Class=col_class), sort=0, idx=6), + THCell(HT.TD('Human',HT.BR(),'Chr', align='left', width=60, Class=col_class), text="human_chr", idx=7), + THCell(HT.TD('Mb Start',HT.BR(),'(hg19)', align='left', width=100, Class=col_class), text="mb_start_hg19", idx=8), + THCell(HT.TD('Gene Description', HT.BR(), HT.BR(), align='left', width=290, Class=col_class), text="description", idx=9), + THCell(HT.TD('PolymiRTS',HT.BR(),'Database', HT.BR(), HT.Href(url='http://compbio.uthsc.edu/miRSNP/', text='>>', target="_blank", Class="normalsize"), + align='left', width=100, Class=col_class), sort=0, idx=10), + THCell(HT.TD('Gene Weaver', HT.BR(), 'Info Content', HT.BR(), HT.Href(url='http://geneweaver.org/', text='>>', target="_blank", Class="normalsize"), + align='left', width=110, Class=col_class), sort=0, idx=11), + ]] + + elif self.species == "rat": + + gene_tblobj_header = [[THCell(HT.TD('Index', HT.BR(), HT.BR(), align='left', width=50, Class=col_class), text="index", idx=0), + THCell(HT.TD('Symbol', HT.BR(), HT.BR(), align='left', width=100, Class=col_class), text="symbol", idx=1), + THCell(HT.TD('Mb Start',HT.BR(),'(rn3)', align='left', width=100, Class=col_class), text="mb_start_rn3", idx=2), + THCell(HT.TD('Length (Kb)', HT.BR(), HT.BR(), align='left', width=100, Class=col_class), text="length", idx=3), + THCell(HT.TD('Avg',HT.BR(),'Expr', HT.BR(), HT.BR(), align='left', width=44, Class=col_class), sort=0, idx=4), + THCell(HT.TD('Mouse',HT.BR(),'Chr', align='left', width=60, Class=col_class), text="mouse_chr", idx=5), + THCell(HT.TD('Mb Start',HT.BR(),'(mm9)', align='left', width=100, Class=col_class), text="mb_start_mm9", idx=6), + THCell(HT.TD('Human',HT.BR(),'Chr', align='left', width=60, Class=col_class), text="human_chr", idx=7), + THCell(HT.TD('Mb Start',HT.BR(),'(hg19)', align='left', width=100, Class=col_class), text="mb_start_hg19", idx=8), + THCell(HT.TD('Gene Description', HT.BR(), HT.BR(), align='left', Class=col_class), text="description", idx=9)]] + + else: + pass + + return gene_tblobj_header + + def getGeneTableBody(self, geneCol, refGene=None): + + tblobj_body = [] #contains table rows + className = "fs13 b1 c222" + + tableIterationsCnt = 0 + if self.species == "mouse": + + # polymiRTS + # http://lily.uthsc.edu:8080/20090422_UTHSC_cuiyan/PolymiRTS_CLS?chrom=2&chrom_from=115&chrom_to=125 + #XZ: We can NOT assume their web service is always on. We must put this block of code in try except. + try: + conn = httplib.HTTPConnection("lily.uthsc.edu:8080") + conn.request("GET", "/20090422_UTHSC_cuiyan/PolymiRTS_CLS?chrom=%s&chrom_from=%s&chrom_to=%s" % (self.genotype[0].name, self.startMb, self.endMb)) + response = conn.getresponse() + data = response.read() + data = data.split() + conn.close() + dic = {} + index = 0 + for i in data: + if index%3==0: + dic[data[index]] = HT.Href(url=data[index+2], text=data[index+1], target="_blank", Class="normalsize") + index = index+1 + except Exception: + dic={} + + for gIndex, theGO in enumerate(geneCol): + + tableIterationsCnt = tableIterationsCnt + 1 + + this_row = [] #container for the cells of each row + selectCheck = HT.Input(type="checkbox", name="searchResult", value=theGO["GeneSymbol"], Class="checkbox", onClick="highlight(this)") #checkbox for each row + + geneLength = (theGO["TxEnd"] - theGO["TxStart"])*1000.0 + tenPercentLength = geneLength*0.0001 + txStart = theGO["TxStart"] + txEnd = theGO["TxEnd"] + theGO["snpDensity"] = theGO["snpCount"]/geneLength + if self.ALEX_DEBUG_BOOL_PRINT_GENE_LIST: + #accessionString = 'http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD=Display&DB=gene&term=%s' % theGO["NM_ID"] + geneIdString = 'http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=%s' % theGO["GeneID"] + + allProbeString = '%s?cmd=sch&gene=%s&alias=1' % (os.path.join(webqtlConfig.CGIDIR, webqtlConfig.SCRIPTFILE), theGO["GeneSymbol"]) + if theGO["snpCount"]: + snpString = HT.Href(url="%s&chr=%s&start=%s&end=%s&geneName=%s&s1=%d&s2=%d" % (os.path.join(webqtlConfig.CGIDIR, 'main.py?FormID=snpBrowser'), + theGO["Chromosome"], theGO["TxStart"], theGO["TxEnd"], theGO["GeneSymbol"], self.diffCol[0], self.diffCol[1]), + text=theGO["snpCount"], target="_blank", Class="normalsize") + else: + snpString = 0 + + mouseStartString = "http://genome.ucsc.edu/cgi-bin/hgTracks?clade=vertebrate&org=Mouse&db=mm9&position=chr" + theGO["Chromosome"] + "%3A" + str(int(theGO["TxStart"] * 1000000.0)) + "-" + str(int(theGO["TxEnd"]*1000000.0)) +"&pix=620&Submit=submit" + + #Used for sorting + mouseStartValue = int(theGO["TxStart"]) + + + #the chromosomes for human 1 are 1qXX.XX + if theGO['humanGene']: + if theGO['humanGene']["TxStart"] == '': + humanStartDisplay = "" + else: + humanStartDisplay = "%0.6f" % theGO['humanGene']["TxStart"] + + humanChr = theGO['humanGene']["Chromosome"] + if humanChr.find('q'): + humanChrSort = humanChr[:humanChr.find("q")].join(humanChr[(humanChr.find("q")+1):]) #value used when sorting table + elif humanChr.find('p'): + humanChrSort = humanChr[:humanChr.find("p")].join(humanChr[(humanChr.find("p")+1):]) #value used when sorting table + else: + humanChrSort = humanChr + humanTxStart = theGO['humanGene']["TxStart"] + + #Used for sorting + humanStartValue = float(theGO['humanGene']["TxStart"]) + + humanStartString = "http://genome.ucsc.edu/cgi-bin/hgTracks?clade=vertebrate&org=Human&db=hg17&position=chr%s:%d-%d" % (humanChr, int(1000000*theGO['humanGene']["TxStart"]), int(1000000*theGO['humanGene']["TxEnd"])) + else: + humanStartString = humanChr = humanChrSort = humanStartDisplay = humanStartValue = "--" + + geneDescription = theGO["GeneDescription"] + if len(geneDescription) > 26: + geneDescription = geneDescription[:26]+"..." + probeSetSearch = HT.Href(allProbeString, HT.Image("/images/webqtl_search.gif", border=0), target="_blank") + + if theGO["snpDensity"] < 0.000001: + snpDensityStr = "0" + else: + snpDensityStr = "%0.6f" % theGO["snpDensity"] + + avgExpr = [] #theGO["avgExprVal"] + if avgExpr in ([], None): + avgExpr = "--" + else: + avgExpr = "%0.6f" % avgExpr + + # polymiRTS + polymiRTS = ' ' + if dic.has_key(theGO["GeneID"]): + polymiRTS = dic[theGO["GeneID"]] + + # If we have a referenceGene then we will show the Literature Correlation + if refGene: + try: + literatureCorrelation = self.getLiteratureCorrelation(self.cursor,refGene,theGO['GeneID']) + except: + literatureCorrelation = "N/A" + + literatureCorrelationString = str(self.getLiteratureCorrelation(self.cursor,refGene,theGO['GeneID']) or "N/A") + + this_row.append(TDCell(HT.TD(tableIterationsCnt, selectCheck, width=30, align='right', Class=className), tableIterationsCnt, tableIterationsCnt)) + this_row.append(TDCell(HT.TD(HT.Href(geneIdString, theGO["GeneSymbol"], target="_blank"), " ", probeSetSearch, align='right', Class=className), theGO["GeneSymbol"], theGO["GeneSymbol"])) + this_row.append(TDCell(HT.TD(HT.Href(mouseStartString, "%0.6f" % txStart, target="_blank"), align='right', Class=className), str(mouseStartValue), mouseStartValue)) + this_row.append(TDCell(HT.TD(HT.Href("javascript:centerIntervalMapOnRange2('%s', " % theGO["Chromosome"]+str(txStart-tenPercentLength) + ", " + str(txEnd+tenPercentLength) + ", document.changeViewForm)", "%0.3f" % geneLength), align='right', Class=className), "%0.3f" % geneLength, geneLength)) + this_row.append(TDCell(HT.TD(snpString, align='right', Class=className), str(theGO["snpCount"]), theGO["snpCount"])) + this_row.append(TDCell(HT.TD(snpDensityStr, align='right', Class=className), snpDensityStr, theGO["snpDensity"])) + this_row.append(TDCell(HT.TD(avgExpr, align='right', Class=className), "--", "--")) + this_row.append(TDCell(HT.TD(humanChr, align='right', Class=className), humanChr, humanChrSort)) + this_row.append(TDCell(HT.TD(HT.Href(humanStartString, humanStartDisplay, target="_blank"), align='right', Class=className), humanStartDisplay, humanStartValue)) + this_row.append(TDCell(HT.TD(literatureCorrelationString, align='right', Class=className), literatureCorrelationString, literatureCorrelation)) + this_row.append(TDCell(HT.TD(geneDescription, align='right', Class=className), geneDescription, geneDescription)) + this_row.append(TDCell(HT.TD(polymiRTS, align='right', Class=className), "", "")) + this_row.append(TDCell(HT.TD("", align='right', Class=className), "", "")) + + else: + this_row.append(TDCell(HT.TD(tableIterationsCnt, selectCheck, width=30, align='right', Class=className), tableIterationsCnt, tableIterationsCnt)) + this_row.append(TDCell(HT.TD(HT.Href(geneIdString, theGO["GeneSymbol"], target="_blank"), " ", probeSetSearch, align='right', Class=className), theGO["GeneSymbol"], theGO["GeneSymbol"])) + this_row.append(TDCell(HT.TD(HT.Href(mouseStartString, "%0.6f" % txStart, target="_blank"), align='right', Class=className), str(mouseStartValue), mouseStartValue)) + this_row.append(TDCell(HT.TD(HT.Href("javascript:centerIntervalMapOnRange2('%s', " % theGO["Chromosome"]+str(txStart-tenPercentLength) + ", " + str(txEnd+tenPercentLength) + ", document.changeViewForm)", "%0.3f" % geneLength), align='right', Class=className), "%0.3f" % geneLength, geneLength)) + this_row.append(TDCell(HT.TD(snpString, align='right', Class=className), str(theGO["snpCount"]), theGO["snpCount"])) + this_row.append(TDCell(HT.TD(snpDensityStr, align='right', Class=className), snpDensityStr, theGO["snpDensity"])) + this_row.append(TDCell(HT.TD(avgExpr, align='right', Class=className), "--", "--")) + this_row.append(TDCell(HT.TD(humanChr, align='right', Class=className), humanChr, humanChrSort)) + this_row.append(TDCell(HT.TD(HT.Href(humanStartString, humanStartDisplay, target="_blank"), align='right', Class=className), humanStartDisplay, humanStartValue)) + this_row.append(TDCell(HT.TD(geneDescription, align='right', Class=className), geneDescription, geneDescription)) + this_row.append(TDCell(HT.TD(polymiRTS, align='right', Class=className), "", "")) + this_row.append(TDCell(HT.TD("", align='right', Class=className), "", "")) + + tblobj_body.append(this_row) + + elif self.species == 'rat': + + for gIndex, theGO in enumerate(geneCol): + + this_row = [] #container for the cells of each row + selectCheck = HT.Input(type="checkbox", name="searchResult", Class="checkbox", onClick="highlight(this)") #checkbox for each row + + webqtlSearch = HT.Href(os.path.join(webqtlConfig.CGIDIR, webqtlConfig.SCRIPTFILE)+"?cmd=sch&gene=%s&alias=1&species=rat" % theGO["GeneSymbol"], HT.Image("/images/webqtl_search.gif", border=0), target="_blank") + + if theGO["GeneID"] != "": + geneSymbolNCBI = HT.Href("http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=%s" % theGO["GeneID"], theGO["GeneSymbol"], Class="normalsize", target="_blanK") + else: + geneSymbolNCBI = theGO["GeneSymbol"] + + geneLength = (float(theGO["TxEnd"]) - float(theGO["TxStart"])) + geneLengthURL = "javascript:centerIntervalMapOnRange2('%s', %f, %f, document.changeViewForm)" % (theGO["Chromosome"], float(theGO["TxStart"])-(geneLength*0.1), float(theGO["TxEnd"])+(geneLength*0.1)) + + avgExprVal = [] + if avgExprVal != "" and avgExprVal: + avgExprVal = "%0.5f" % float(avgExprVal) + else: + avgExprVal = "" + + #Mouse Gene + if theGO['mouseGene']: + mouseChr = theGO['mouseGene']["Chromosome"] + mouseTxStart = theGO['mouseGene']["TxStart"] + else: + mouseChr = mouseTxStart = "" + + #the chromosomes for human 1 are 1qXX.XX + if theGO['humanGene']: + humanChr = theGO['humanGene']["Chromosome"] + if 'q' in humanChr: + humanChrSort = humanChr[:humanChr.find("q")].join(humanChr[(humanChr.find("q")+1):]) #value used when sorting table + elif 'p' in humanChr: + humanChrSort = humanChr[:humanChr.find("p")].join(humanChr[(humanChr.find("p")+1):]) #value used when sorting table + else: + humanChrSort = humanChr + humanTxStart = theGO['humanGene']["TxStart"] + else: + humanChr = humanTxStart = humanChrSort = "" + + geneDesc = theGO["GeneDescription"] + if geneDesc == "---": + geneDesc = "" + + """ + if len(geneDesc) > 40: + geneDesc = gene0So apparently Angola prison (which used to be a slave plantation) has a rodeo that they invite the general public to. +The prisoners are not trained before hand +But its cool because its completely voluntary. +And by voluntary, according to HFG when I talked to him, they have a choice between doing it or door number two and "door number 2 is... rather worse than volunteering"Desc[:37] + "..." + """ + + this_row.append(TDCell(HT.TD(gIndex + 1, selectCheck, align='left', Class=className), str(gIndex+1), gIndex+1)) + this_row.append(TDCell(HT.TD(webqtlSearch, geneSymbolNCBI, align='left', Class=className), theGO["GeneSymbol"], theGO["GeneSymbol"])) + this_row.append(TDCell(HT.TD(theGO["TxStart"], align='left', Class=className), theGO["TxStart"], theGO["TxStart"])) + this_row.append(TDCell(HT.TD(HT.Href(geneLengthURL, "%0.3f" % (geneLength*1000.0)), align='left', Class=className), "%0.3f" % (geneLength*1000.0), (geneLength*1000.0))) + this_row.append(TDCell(HT.TD(avgExprVal, align='left', Class=className), "", "")) + this_row.append(TDCell(HT.TD(mouseChr, align='left', Class=className), mouseChr, mouseChr)) + this_row.append(TDCell(HT.TD(mouseTxStart, align='left', Class=className), mouseTxStart, mouseTxStart)) + this_row.append(TDCell(HT.TD(humanChr, align='left', Class=className), humanChr, humanChrSort)) + this_row.append(TDCell(HT.TD(humanTxStart, align='left', Class=className), humanTxStart, humanTxStart)) + this_row.append(TDCell(HT.TD(geneDesc, align='left', Class=className), geneDesc, geneDesc)) + + tblobj_body.append(this_row) + + else: + pass + + return tblobj_body + + + def getSortByValue(self): + + sortby = ("", "") + + return sortby \ No newline at end of file diff --git a/wqflask/wqflask/templates/marker_regression_gn1.html b/wqflask/wqflask/templates/marker_regression_gn1.html new file mode 100644 index 00000000..29f69dea --- /dev/null +++ b/wqflask/wqflask/templates/marker_regression_gn1.html @@ -0,0 +1,204 @@ + + + + +Mapping + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+ + + + +
+
+ + +
+

Map Viewer: Whole Genome

+

+ Population: {{ dataset.species }} {{ dataset.group.name }}
+ Database: {{ dataset.fullname }}
+ Trait ID: {{ marker.name }}
+ {% if this_trait.symbol != None %} + Gene Symbol: this_trait.symbol
+ {% if this_trait.dataset.type != 'Publish' %} + Location: {{ this_trait.location_fmt }} + {% endif %} +

+

+
Download results in tab-delimited text format.

  +
+
Chr: + + +
View: + to +Mb *
Units: +LRS +LOD Glossary
+units on Y-axis (0 for default)
Width: +pixels (minimum=1400)
  +Permutation Test Glossary
+Bootstrap Test Glossary
+Allele Effects Glossary
+SNP Track Glossary *
+Gene Track *
+Interval Analyst *
+Haplotype Analyst *
+Legend
+2X Plot
* only apply to single chromosome physical mapping
+ + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + +
+
+ + +Itvl_bnCx5c3U.png +

+


A positive additive coefficient (green line) indicates that DBA/2J alleles increase trait values. In contrast, a negative additive coefficient (red line) indicates that C57BL/6J alleles increase trait values.

+

+
Histogram of Permutation Test
Total of 1000 permutations
+

+Download Permutation Results

+
+ + + + + + + + + + \ No newline at end of file diff --git a/wqflask/wqflask/templates/show_trait_statistics_new.html b/wqflask/wqflask/templates/show_trait_statistics_new.html index 1932d968..34fa2216 100755 --- a/wqflask/wqflask/templates/show_trait_statistics_new.html +++ b/wqflask/wqflask/templates/show_trait_statistics_new.html @@ -13,9 +13,11 @@
  • Probability Plot
    • + {% if g.user_session.user_ob %}
  • Scatterplot Matrix
    • + {% endif %} @@ -127,6 +129,7 @@
    --> + {% if g.user_session.user_ob %}
    @@ -141,6 +144,7 @@
    + {% endif %} diff --git a/wqflask/wqflask/views.py b/wqflask/wqflask/views.py index 588433f0..3b100fa6 100755 --- a/wqflask/wqflask/views.py +++ b/wqflask/wqflask/views.py @@ -42,7 +42,7 @@ from wqflask.show_trait import show_trait from wqflask.show_trait import export_trait_data from wqflask.heatmap import heatmap from wqflask.marker_regression import marker_regression -#from wqflask.marker_regression import marker_regression_gn1 +from wqflask.marker_regression import marker_regression_gn1 from wqflask.interval_mapping import interval_mapping from wqflask.correlation import show_corr_results from wqflask.correlation_matrix import show_corr_matrix @@ -384,7 +384,7 @@ def marker_regression_page(): #causeerror - #gn1_template_vars = marker_regression_gn1.MarkerRegression(template_vars) + gn1_template_vars = marker_regression_gn1.MarkerRegression(result) #qtl_length = len(result['js_data']['qtl_results']) #print("qtl_length:", qtl_length) -- cgit v1.2.3 From 97b83d20a5f6896614024a3cc40535bfb738ef51 Mon Sep 17 00:00:00 2001 From: zsloan Date: Sat, 12 Dec 2015 00:01:06 +0000 Subject: Changed loop drawing qtl curve to fix some issues; still need to make it draw to different chr areas though --- .gitignore | 1 + wqflask/base/webqtlConfig.py | 2 +- .../marker_regression/marker_regression_gn1.py | 65 ++++++++++++++-------- wqflask/wqflask/views.py | 8 +-- 4 files changed, 48 insertions(+), 28 deletions(-) (limited to 'wqflask/base') diff --git a/.gitignore b/.gitignore index 1ab1e727..f4693a9a 100644 --- a/.gitignore +++ b/.gitignore @@ -7,3 +7,4 @@ web/new_genotypes/HSNIH.json wqflask/secure_server.py wqflask/base/webqtlConfig.py +wqflask/output/* diff --git a/wqflask/base/webqtlConfig.py b/wqflask/base/webqtlConfig.py index 330fec56..4f9b3af3 100755 --- a/wqflask/base/webqtlConfig.py +++ b/wqflask/base/webqtlConfig.py @@ -55,7 +55,7 @@ COMMON_LIB = GNROOT + 'support/admin' HTMLPATH = GNROOT + 'genotype_files/' PYLMM_PATH = '/home/zas1024/plink_gemma/' SNP_PATH = '/home/zas1024/snps/' -IMGDIR = GNROOT + '/wqflask/wqflask/images/' +IMGDIR = GNROOT + '/wqflask/output/' IMAGESPATH = HTMLPATH + 'images/' UPLOADPATH = IMAGESPATH + 'upload/' TMPDIR = '/home/zas1024/tmp/' # Will remove this and dependent items later diff --git a/wqflask/wqflask/marker_regression/marker_regression_gn1.py b/wqflask/wqflask/marker_regression/marker_regression_gn1.py index f2fc12a4..c2cd5e97 100644 --- a/wqflask/wqflask/marker_regression/marker_regression_gn1.py +++ b/wqflask/wqflask/marker_regression/marker_regression_gn1.py @@ -37,13 +37,14 @@ from flask import Flask, g from htmlgen import HTMLgen2 as HT + from utility import helper_functions from utility import Plot from base import webqtlConfig #from intervalAnalyst import GeneUtil #from base.webqtlTrait import webqtlTrait #from base.templatePage import templatePage -#from utility import webqtlUtil +from utility import webqtlUtil #from utility.THCell import THCell #from utility.TDCell import TDCell #from dbFunction import webqtlDatabaseFunction @@ -507,19 +508,16 @@ class MarkerRegression(object): ################################################################ # Plots goes here ################################################################ - print("BEFORE GN1 PLOT") if self.plotScale != 'physic' or self.multipleInterval: showLocusForm = webqtlUtil.genRandStr("fm_") else: showLocusForm = "" - print("BEFORE PIL CANVAS") intCanvas = pid.PILCanvas(size=(self.graphWidth,self.graphHeight)) - print("BEFORE PLOTINTMAPPING") gifmap = self.plotIntMapping(intCanvas, startMb = self.startMb, endMb = self.endMb, showLocusForm= showLocusForm) print("AFTER PLOTINTMAPPING") filename= webqtlUtil.genRandStr("Itvl_") - intCanvas.save(os.path.join(webqtlConfig.IMGDIR, filename), format='png') + intCanvas.save(os.path.join(webqtlConfig.IMGDIR, filename), format='jpeg') intImg=HT.Image('/image/'+filename+'.png', border=0, usemap='#WebQTLImageMap') #Scales plot differently for high resolution @@ -743,7 +741,6 @@ class MarkerRegression(object): endPixelX = (xLeftOffset + plotWidth) #Drawing Area Height - print("DRAWING AREA HEIGHT") drawAreaHeight = plotHeight if self.plotScale == 'physic' and self.selectedChr > -1: drawAreaHeight -= self.ENSEMBL_BAND_HEIGHT + self.UCSC_BAND_HEIGHT+ self.WEBQTL_BAND_HEIGHT + 3*self.BAND_SPACING+ 10*zoom @@ -769,7 +766,6 @@ class MarkerRegression(object): newoffset = (xLeftOffset, xRightOffset, yTopOffset, yBottomOffset) # Draw the alternating-color background first and get plotXScale - print("DRAW BACKGROUND") plotXScale = self.drawGraphBackground(canvas, gifmap, offset=newoffset, zoom= zoom, startMb=startMb, endMb = endMb) #draw bootstap @@ -778,7 +774,6 @@ class MarkerRegression(object): # Draw clickable region and gene band if selected if self.plotScale == 'physic' and self.selectedChr > -1: - print("DRAW CLICKABLE REGION") self.drawClickBand(canvas, gifmap, plotXScale, offset=newoffset, zoom = zoom, startMb=startMb, endMb = endMb) if self.geneChecked and self.geneCol: self.drawGeneBand(canvas, gifmap, plotXScale, offset=newoffset, zoom = zoom, startMb=startMb, endMb = endMb) @@ -786,18 +781,14 @@ class MarkerRegression(object): self.drawSNPTrackNew(canvas, offset=newoffset, zoom = 2*zoom, startMb=startMb, endMb = endMb) ## BEGIN HaplotypeAnalyst if self.haplotypeAnalystChecked: - print("DRAW HAPLOTYPE") self.drawHaplotypeBand(canvas, gifmap, plotXScale, offset=newoffset, zoom = zoom, startMb=startMb, endMb = endMb) ## END HaplotypeAnalyst # Draw X axis - print("DRAW X AXIS") self.drawXAxis(canvas, drawAreaHeight, gifmap, plotXScale, showLocusForm, offset=newoffset, zoom = zoom, startMb=startMb, endMb = endMb) # Draw QTL curve - print("DRAW QTL CURVE") self.drawQTL(canvas, drawAreaHeight, gifmap, plotXScale, offset=newoffset, zoom= zoom, startMb=startMb, endMb = endMb) #draw legend - print("DRAW LEGEND") if self.multipleInterval: self.drawMultiTraitName(fd, canvas, gifmap, showLocusForm, offset=newoffset) elif self.legendChecked: @@ -806,7 +797,6 @@ class MarkerRegression(object): pass #draw position, no need to use a separate function - print("DRAW PROBESET POSITION") if self.genotype.Mbmap: self.drawProbeSetPosition(canvas, plotXScale, offset=newoffset, zoom = zoom) @@ -1823,7 +1813,7 @@ class MarkerRegression(object): lodm = self.LODFACTOR else: lodm = 1.0 - + if self.lrsMax <= 0: #sliding scale if "lrs_value" in self.qtlresults[0]: LRSMax = max([result['lrs_value'] for result in self.qtlresults]) @@ -1874,6 +1864,7 @@ class MarkerRegression(object): #"Significant" and "Suggestive" Drawing Routine # ======= Draw the thick lines for "Significant" and "Suggestive" ===== (crowell: I tried to make the SNPs draw over these lines, but piddle wouldn't have it...) + print("DRAW SUGGESTIVE/SIGNFICANT LINES") if self.permChecked and not self.multipleInterval: significantY = yZero - self.significance*LRSHeightThresh/LRSMax suggestiveY = yZero - self.suggestive*LRSHeightThresh/LRSMax @@ -1912,23 +1903,37 @@ class MarkerRegression(object): if zoom == 2: lrsEdgeWidth = 2 * lrsEdgeWidth + print("DRAW QTL RESULT CURVE") + + LRSCoordXY = [] + AdditiveCoordXY = [] + DominanceCoordXY = [] + + previous_chr = 1 + previous_chr_as_int = 1 for i, qtlresult in enumerate(self.qtlresults): m = 0 startPosX = xLeftOffset thisLRSColor = self.colorCollection[0] - for j, _chr in enumerate(self.genotype): - LRSCoordXY = [] - AdditiveCoordXY = [] - DominanceCoordXY = [] - for k, _locus in enumerate(_chr): + #for j, _chr in enumerate(self.genotype): + if 1 == 1: + #LRSCoordXY = [] + #AdditiveCoordXY = [] + #DominanceCoordXY = [] + #for k, _locus in enumerate(_chr): + if 1 == 1: if self.plotScale == 'physic': - Xc = startPosX + (_locus.Mb-startMb)*plotXScale + #Xc = startPosX + (_locus.Mb-startMb)*plotXScale + Xc = startPosX + (qtlresult['Mb']-startMb)*plotXScale else: - Xc = startPosX + (_locus.cM-_chr[0].cM)*plotXScale + #Xc = startPosX + (_locus.cM-_chr[0].cM)*plotXScale + Xc = startPosX + (qtlresult['cM']-qtlresult[0]['cM'])*plotXScale + # updated by NL 06-18-2011: # fix the over limit LRS graph issue since genotype trait may give infinite LRS; # for any lrs is over than 460(LRS max in this system), it will be reset to 460 if qtlresult['lrs_value'] > 460 or qtlresult['lrs_value']=='inf': + #if self.qtlresults[j]['lrs_value'] > 460 or self.qtlresults[j]['lrs_value']=='inf': Yc = yZero - webqtlConfig.MAXLRS*LRSHeightThresh/LRSMax else: Yc = yZero - qtlresult['lrs_value']*LRSHeightThresh/LRSMax @@ -1943,7 +1948,7 @@ class MarkerRegression(object): # Yc = yZero - qtlresult[m].dominance*DominanceHeightThresh/dominanceMax # DominanceCoordXY.append((Xc, Yc)) m += 1 - canvas.drawPolygon(LRSCoordXY,edgeColor=thisLRSColor,closed=0, edgeWidth=lrsEdgeWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + #canvas.drawPolygon(LRSCoordXY,edgeColor=thisLRSColor,closed=0, edgeWidth=lrsEdgeWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) lineWidth = 1 if not self.multipleInterval and self.additiveChecked: @@ -2004,7 +2009,21 @@ class MarkerRegression(object): canvas.drawLine(Xc0, Yc0, Xc, Yc, color=plusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) else: canvas.drawLine(Xc0, yZero - (Yc0-yZero), Xc, yZero - (Yc-yZero), color=minusColor, width=lineWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) - startPosX += (self.ChrLengthDistList[j]+self.GraphInterval)*plotXScale + + print("previous_chr:", previous_chr_as_int) + startPosX += (self.ChrLengthDistList[previous_chr_as_int-1]+self.GraphInterval)*plotXScale + #startPosX += (self.ChrLengthDistList[j]+self.GraphInterval)*plotXScale + + if qtlresult['chr'] != previous_chr: + previous_chr = qtlresult['chr'] + try: + previous_chr_as_int = int(previous_chr) + except: + previous_chr_as_int += 1 + + canvas.drawPolygon(LRSCoordXY,edgeColor=thisLRSColor,closed=0, edgeWidth=lrsEdgeWidth, clipX=(xLeftOffset, xLeftOffset + plotWidth)) + + print("AFTER QTL CURVE") ###draw additive scale if not self.multipleInterval and self.additiveChecked: diff --git a/wqflask/wqflask/views.py b/wqflask/wqflask/views.py index 4446b431..c17d6274 100755 --- a/wqflask/wqflask/views.py +++ b/wqflask/wqflask/views.py @@ -385,10 +385,10 @@ def marker_regression_page(): #causeerror - #print("TESTING GN1!!!") - #gn1_template_vars = marker_regression_gn1.MarkerRegression(result).__dict__ - #print("gn1_template_vars:", gn1_template_vars) - #causeerror + print("TESTING GN1!!!") + gn1_template_vars = marker_regression_gn1.MarkerRegression(result).__dict__ + print("gn1_template_vars:", gn1_template_vars) + causeerror #qtl_length = len(result['js_data']['qtl_results']) -- cgit v1.2.3