diff options
| author | Pjotr Prins | 2016-10-07 10:34:32 +0000 |
|---|---|---|
| committer | Pjotr Prins | 2016-10-07 10:34:32 +0000 |
| commit | 420fd69ceda63871e9f6755112769c5615ed45f6 (patch) | |
| tree | d834a125aaf99dcd04868a8907b097445f576b4b /wqflask | |
| parent | 0f602fd058934feaaa37eb72d055bfcfcfc9ef8f (diff) | |
| parent | 28da8f4304f406b4eff5ad68757735a0cb524e94 (diff) | |
| download | genenetwork2-420fd69ceda63871e9f6755112769c5615ed45f6.tar.gz | |
Merge branch 'master' into chfi
Diffstat (limited to 'wqflask')
62 files changed, 617 insertions, 485 deletions
diff --git a/wqflask/base/data_set.py b/wqflask/base/data_set.py index 1b4e1195..fddfce58 100644 --- a/wqflask/base/data_set.py +++ b/wqflask/base/data_set.py @@ -107,7 +107,8 @@ Publish or ProbeSet. E.g. else: new_type = "ProbeSet" self.datasets[short_dataset_name] = new_type - logger.info("datasets",self.datasets) + # Set LOG_LEVEL_DEBUG=5 to see the following: + logger.debugf(5,"datasets",self.datasets) def __call__(self, name): return self.datasets[name] diff --git a/wqflask/base/trait.py b/wqflask/base/trait.py index 900e050c..32032ba7 100644 --- a/wqflask/base/trait.py +++ b/wqflask/base/trait.py @@ -363,7 +363,7 @@ class GeneralTrait(object): FROM Homologene, Species, InbredSet WHERE - Homologene.GeneId =%s AND + Homologene.GeneId ='%s' AND InbredSet.Name = '%s' AND InbredSet.SpeciesId = Species.Id AND Species.TaxonomyId = Homologene.TaxonomyId diff --git a/wqflask/base/webqtlCaseData.py b/wqflask/base/webqtlCaseData.py index 8df9939e..2f88f778 100644 --- a/wqflask/base/webqtlCaseData.py +++ b/wqflask/base/webqtlCaseData.py @@ -16,8 +16,6 @@ # 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 diff --git a/wqflask/runserver.py b/wqflask/runserver.py index 12ec904e..0342b7ad 100644 --- a/wqflask/runserver.py +++ b/wqflask/runserver.py @@ -16,34 +16,37 @@ GREEN = '\033[92m' BOLD = '\033[1m' ENDC = '\033[0m' -logger.info("GN2 is running. Visit %shttp://localhost:5003/%s" % (BLUE,ENDC)) - import os app.config['SECRET_KEY'] = os.urandom(24) -from utility.tools import WEBSERVER_MODE +from utility.tools import WEBSERVER_MODE,get_setting_int + +port = get_setting_int("SERVER_PORT") + +logger.info("GN2 is running. Visit %shttp://localhost:%s/%s" % (BLUE,port,ENDC)) werkzeug_logger = logging.getLogger('werkzeug') if WEBSERVER_MODE == 'DEBUG': app.run(host='0.0.0.0', - port=app.config['SERVER_PORT'], + port=port, debug=True, - use_debugger=True, + use_debugger=False, threaded=False, + processes=0, use_reloader=True) elif WEBSERVER_MODE == 'DEV': werkzeug_logger.setLevel(logging.WARNING) app.run(host='0.0.0.0', - port=app.config['SERVER_PORT'], + port=port, debug=False, use_debugger=False, threaded=False, processes=0, use_reloader=True) -else: #production mode +else: # staging/production modes app.run(host='0.0.0.0', - port=app.config['SERVER_PORT'], + port=port, debug=False, use_debugger=False, threaded=True, diff --git a/wqflask/utility/helper_functions.py b/wqflask/utility/helper_functions.py index 149ee553..377f6b26 100644 --- a/wqflask/utility/helper_functions.py +++ b/wqflask/utility/helper_functions.py @@ -5,19 +5,21 @@ from base import data_set from base.species import TheSpecies from wqflask import user_manager +import logging +logger = logging.getLogger(__name__ ) def get_species_dataset_trait(self, start_vars): #assert type(read_genotype) == type(bool()), "Expecting boolean value for read_genotype" self.dataset = data_set.create_dataset(start_vars['dataset']) - print("After creating dataset") + logger.debug("After creating dataset") self.species = TheSpecies(dataset=self.dataset) - print("After creating species") + logger.debug("After creating species") self.this_trait = GeneralTrait(dataset=self.dataset, name=start_vars['trait_id'], cellid=None, get_qtl_info=True) - print("After creating trait") + logger.debug("After creating trait") #if read_genotype: #self.dataset.group.read_genotype_file() @@ -27,7 +29,7 @@ def get_species_dataset_trait(self, start_vars): def get_trait_db_obs(self, trait_db_list): if isinstance(trait_db_list, basestring): trait_db_list = trait_db_list.split(",") - + self.trait_list = [] for trait in trait_db_list: data, _separator, hmac = trait.rpartition(':') @@ -38,4 +40,4 @@ def get_trait_db_obs(self, trait_db_list): trait_ob = GeneralTrait(dataset=dataset_ob, name=trait_name, cellid=None) - self.trait_list.append((trait_ob, dataset_ob))
\ No newline at end of file + self.trait_list.append((trait_ob, dataset_ob)) diff --git a/wqflask/utility/logger.py b/wqflask/utility/logger.py index ddc0ea82..bacb0aa4 100644 --- a/wqflask/utility/logger.py +++ b/wqflask/utility/logger.py @@ -31,6 +31,7 @@ import string from inspect import isfunction from pprint import pformat as pf from inspect import stack +import datetime from utility.tools import LOG_LEVEL, LOG_LEVEL_DEBUG, LOG_SQL, LOG_FORMAT @@ -49,11 +50,20 @@ class GNLogger: self.logger.setLevel(value) def debug(self,*args): + """Call logging.debug for multiple args. Use (lazy) debugf and +level=num to filter on LOG_LEVEL_DEBUG. + + """ + self.collect(self.logger.debug,*args) + + def debug20(self,*args): """Call logging.debug for multiple args. Use level=num to filter on LOG_LEVEL_DEBUG (NYI). """ - self.collect(self.logger.debug,*args) + if level <= LOG_LEVEL_DEBUG: + if self.logger.getEffectiveLevel() < 20: + self.collect(self.logger.debug,*args) def info(self,*args): """Call logging.info for multiple args""" @@ -66,7 +76,10 @@ LOG_LEVEL_DEBUG (NYI). def error(self,*args): """Call logging.error for multiple args""" - self.collect(self.logger.error,*args) + now = datetime.datetime.utcnow() + time_str = now.strftime('%H:%M:%S UTC %Y%m%d') + l = [time_str]+list(args) + self.collect(self.logger.error,*l) def infof(self,*args): """Call logging.info for multiple args lazily""" @@ -75,7 +88,10 @@ LOG_LEVEL_DEBUG (NYI). self.collectf(self.logger.debug,*args) def debugf(self,level=0,*args): - """Call logging.debug for multiple args lazily""" + """Call logging.debug for multiple args lazily and handle + LOG_LEVEL_DEBUG correctly + + """ # only evaluate function when logging if level <= LOG_LEVEL_DEBUG: if self.logger.getEffectiveLevel() < 20: diff --git a/wqflask/utility/tools.py b/wqflask/utility/tools.py index 907b0d6a..23d6fb62 100644 --- a/wqflask/utility/tools.py +++ b/wqflask/utility/tools.py @@ -3,6 +3,7 @@ import os import sys +import json from wqflask import app @@ -10,6 +11,8 @@ from wqflask import app import logging logger = logging.getLogger(__name__ ) +OVERRIDES = {} + def get_setting(command_id,guess=None): """Resolve a setting from the environment or the global settings in app.config, with valid_path is a function checking whether the @@ -45,13 +48,15 @@ def get_setting(command_id,guess=None): logger.debug("Looking for "+command_id+"\n") command = value(os.environ.get(command_id)) if command is None or command == "": - # ---- Check whether setting exists in app - command = value(app.config.get(command_id)) + command = OVERRIDES.get(command_id) if command is None: - command = value(guess) - if command is None or command == "": - print command - raise Exception(command_id+' setting unknown or faulty (update default_settings.py?).') + # ---- Check whether setting exists in app + command = value(app.config.get(command_id)) + if command is None: + command = value(guess) + if command is None or command == "": + # print command + raise Exception(command_id+' setting unknown or faulty (update default_settings.py?).') logger.debug("Set "+command_id+"="+str(command)) return command @@ -93,6 +98,10 @@ def gemma_command(guess=None): def plink_command(guess=None): return valid_bin(get_setting("PLINK_COMMAND",guess)) +def flat_file_exists(subdir): + base = get_setting("GENENETWORK_FILES") + return valid_path(base+"/"+subdir) + def flat_files(subdir=None): base = get_setting("GENENETWORK_FILES") if subdir: @@ -104,6 +113,7 @@ def assert_dir(dir): raise Exception("ERROR: can not find directory "+dir) return dir + def mk_dir(dir): if not valid_path(dir): os.makedirs(dir) @@ -164,18 +174,20 @@ def show_settings(): log_level = getattr(logging, LOG_LEVEL.upper()) logging.basicConfig(level=log_level) + logger.info(OVERRIDES) logger.info(BLUE+"Mr. Mojo Risin 2"+ENDC) - print "runserver.py: ****** The webserver has the following configuration ******" + print "runserver.py: ****** Webserver configuration ******" keylist = app.config.keys() keylist.sort() for k in keylist: try: - print("%s %s%s%s%s" % (k,BLUE,BOLD,get_setting(k),ENDC)) + print("%s: %s%s%s%s" % (k,BLUE,BOLD,get_setting(k),ENDC)) except: - print("%s %s%s%s%s" % (k,GREEN,BOLD,app.config[k],ENDC)) + print("%s: %s%s%s%s" % (k,GREEN,BOLD,app.config[k],ENDC)) # Cached values +HOME = get_setting('HOME') WEBSERVER_MODE = get_setting('WEBSERVER_MODE') GN_SERVER_URL = get_setting('GN_SERVER_URL') SQL_URI = get_setting('SQL_URI') @@ -187,9 +199,25 @@ LOG_BENCH = get_setting_bool('LOG_BENCH') LOG_FORMAT = "%(message)s" # not yet in use USE_REDIS = get_setting_bool('USE_REDIS') USE_GN_SERVER = get_setting_bool('USE_GN_SERVER') -GENENETWORK_FILES = get_setting_bool('GENENETWORK_FILES') + +GENENETWORK_FILES = get_setting('GENENETWORK_FILES') PYLMM_COMMAND = pylmm_command() GEMMA_COMMAND = gemma_command() PLINK_COMMAND = plink_command() TEMPDIR = tempdir() + +from six import string_types + +if os.environ.get('WQFLASK_OVERRIDES'): + jsonfn = get_setting('WQFLASK_OVERRIDES') + logger.error("WQFLASK_OVERRIDES: %s" % jsonfn) + with open(jsonfn) as data_file: + overrides = json.load(data_file) + for k in overrides: + cmd = overrides[k] + if isinstance(cmd, string_types): + OVERRIDES[k] = eval(cmd) + else: + OVERRIDES[k] = cmd + logger.debug(OVERRIDES) diff --git a/wqflask/wqflask/__init__.py b/wqflask/wqflask/__init__.py index af271d02..2188ce17 100644 --- a/wqflask/wqflask/__init__.py +++ b/wqflask/wqflask/__init__.py @@ -14,11 +14,7 @@ app = Flask(__name__) app.config.from_object('cfg.default_settings') # Get the defaults from cfg.default_settings app.config.from_envvar('WQFLASK_SETTINGS') # See http://flask.pocoo.org/docs/config/#configuring-from-files - -logger.debug("System path is") -logger.debug(sys.path) -logger.debug("App.config is") -logger.debug(app.config) +# Note we also use WQFLASK_OVERRIDES app.jinja_env.globals.update( undefined = jinja2.StrictUndefined, diff --git a/wqflask/wqflask/collect.py b/wqflask/wqflask/collect.py index 7e7aba89..81d03d6c 100644 --- a/wqflask/wqflask/collect.py +++ b/wqflask/wqflask/collect.py @@ -164,7 +164,7 @@ class UserCollection(object): if not uc: return create_new("Default") else: - uc = model.UserCollection.query.get(params['existing_collection']) + uc = model.UserCollection.query.get(params['existing_collection'].split(":")[0]) members = list(uc.members_as_set()) #set(json.loads(uc.members)) len_before = len(members) @@ -218,7 +218,6 @@ def collections_add(): anon_collections = user_manager.AnonUser().get_collections() collection_names = [] for collection in anon_collections: - print("COLLECTION:", collection) collection_names.append({'id':collection['id'], 'name':collection['name']}) return render_template("collections/add.html", traits = traits, @@ -229,21 +228,17 @@ def collections_add(): @app.route("/collections/new") def collections_new(): params = request.args - #print("request.args in collections_new are:", params) - - collection_name = params['new_collection'] - if "anonymous_add" in params: - AnonCollection(name=collection_name).add_traits(params, "Default") - return redirect(url_for('view_collection')) if "sign_in" in params: return redirect(url_for('login')) if "create_new" in params: print("in create_new") + collection_name = params['new_collection'] return create_new(collection_name) elif "add_to_existing" in params: print("in add to existing") + collection_name = params['existing_collection'].split(":")[1] if g.user_session.logged_in: return UserCollection().add_traits(params, collection_name) else: @@ -251,7 +246,6 @@ def collections_new(): ac.add_traits(params) return redirect(url_for('view_collection', collection_id=ac.id)) else: - print("ELSE") CauseAnError @@ -288,7 +282,6 @@ def create_new(collection_name): ac = AnonCollection(collection_name) ac.changed_timestamp = datetime.datetime.utcnow().strftime('%b %d %Y %I:%M%p') ac.add_traits(params) - print("Collection ID:", ac.id) return redirect(url_for('view_collection', collection_id=ac.id)) @app.route("/collections/list") @@ -367,7 +360,6 @@ def view_collection(): uc_id = params['uc_id'] uc = model.UserCollection.query.get(uc_id) traits = json.loads(uc.members) - print("traits are:", traits) else: user_collections = json.loads(Redis.get(user_manager.AnonUser().key)) this_collection = {} @@ -384,7 +376,6 @@ def view_collection(): json_version = [] for atrait in traits: - print("atrait is:", atrait) name, dataset_name = atrait.split(':') trait_ob = trait.GeneralTrait(name=name, dataset_name=dataset_name) @@ -393,8 +384,6 @@ def view_collection(): json_version.append(trait_ob.jsonable()) - print("trait_obs:", trait_obs) - if "uc_id" in params: collection_info = dict(trait_obs=trait_obs, uc = uc) diff --git a/wqflask/wqflask/marker_regression/marker_regression.py b/wqflask/wqflask/marker_regression/marker_regression.py index d2b27991..37ee42a7 100644 --- a/wqflask/wqflask/marker_regression/marker_regression.py +++ b/wqflask/wqflask/marker_regression/marker_regression.py @@ -35,12 +35,15 @@ from utility import helper_functions from utility import Plot, Bunch from utility import temp_data from utility.benchmark import Bench -from wqflask.marker_regression import gemma_mapping +from wqflask.marker_regression import gemma_mapping, rqtl_mapping from utility.tools import locate, locate_ignore_error, PYLMM_COMMAND, GEMMA_COMMAND, PLINK_COMMAND, TEMPDIR from utility.external import shell from base.webqtlConfig import TMPDIR, GENERATED_TEXT_DIR +import utility.logger +logger = utility.logger.getLogger(__name__ ) + class MarkerRegression(object): def __init__(self, start_vars, temp_uuid): @@ -166,7 +169,10 @@ class MarkerRegression(object): self.model = start_vars['mapmodel_rqtl_geno'] if start_vars['pair_scan'] == "true": self.pair_scan = True - results = self.run_rqtl_geno() + if self.permCheck and self.num_perm > 0: + perm_output, self.suggestive, self.significant, results = rqtl_mapping.run_rqtl_geno(self.vals, self.dataset, self.method, self.model, self.permCheck, self.num_perm, self.do_control, self.control_marker, self.manhattan_plot, self.pair_scan) + else: + results = rqtl_mapping.run_rqtl_geno(self.vals, self.dataset, self.method, self.model, self.permCheck, self.num_perm, self.do_control, self.control_marker, self.manhattan_plot, self.pair_scan) elif self.mapping_method == "reaper": if "startMb" in start_vars: #ZS: Check if first time page loaded, so it can default to ON if "additiveCheck" in start_vars: @@ -194,16 +200,17 @@ class MarkerRegression(object): self.control_marker = start_vars['control_marker'] self.do_control = start_vars['do_control'] + logger.info("Running qtlreaper") results = self.gen_reaper_results() elif self.mapping_method == "plink": results = self.run_plink() elif self.mapping_method == "pylmm": - print("RUNNING PYLMM") + logger.debug("RUNNING PYLMM") if self.num_perm > 0: self.run_permutations(str(temp_uuid)) results = self.gen_data(str(temp_uuid)) else: - print("RUNNING NOTHING") + logger.debug("RUNNING NOTHING") if self.pair_scan == True: self.qtl_results = [] @@ -257,9 +264,9 @@ 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']) + # logger.debug("lod score is:", qtl['lod_score']) if qtl['chr'] == highest_chr and highest_chr != "X" and highest_chr != "X/Y": - #print("changing to X") + #logger.debug("changing to X") self.json_data['chr'].append("X") else: self.json_data['chr'].append(str(qtl['chr'])) @@ -277,7 +284,7 @@ class MarkerRegression(object): self.json_data['chrnames'].append([self.species.chromosomes.chromosomes[key].name, self.species.chromosomes.chromosomes[key].mb_length]) chromosome_mb_lengths[key] = self.species.chromosomes.chromosomes[key].mb_length - # print("json_data:", self.json_data) + # logger.debug("json_data:", self.json_data) self.js_data = dict( result_score_type = self.score_type, @@ -305,7 +312,7 @@ class MarkerRegression(object): self.dataset.group.name, self.dataset.group.name, self.dataset.group.name) - #print("gemma_command:" + gemma_command) + #logger.debug("gemma_command:" + gemma_command) os.system(gemma_command) @@ -327,7 +334,7 @@ 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) + #logger.debug("p_values: ", p_values) return included_markers, p_values def gen_pheno_txt_file(self): @@ -349,200 +356,13 @@ class MarkerRegression(object): count, p_values = self.parse_rqtl_output(plink_output_filename) - def geno_to_rqtl_function(self): # TODO: Need to figure out why some genofiles have the wrong format and don't convert properly - - ro.r(""" - trim <- function( x ) { gsub("(^[[:space:]]+|[[:space:]]+$)", "", x) } - - getGenoCode <- function(header, name = 'unk'){ - mat = which(unlist(lapply(header,function(x){ length(grep(paste('@',name,sep=''), x)) })) == 1) - return(trim(strsplit(header[mat],':')[[1]][2])) - } - - GENOtoCSVR <- function(genotypes = '%s', out = 'cross.csvr', phenotype = NULL, sex = NULL, verbose = FALSE){ - header = readLines(genotypes, 40) # Assume a geno header is not longer than 40 lines - toskip = which(unlist(lapply(header, function(x){ length(grep("Chr\t", x)) })) == 1)-1 # Major hack to skip the geno headers - - genocodes <- c(getGenoCode(header, 'mat'), getGenoCode(header, 'het'), getGenoCode(header, 'pat')) # Get the genotype codes - type <- getGenoCode(header, 'type') - genodata <- read.csv(genotypes, sep='\t', skip=toskip, header=TRUE, na.strings=getGenoCode(header,'unk'), colClasses='character', comment.char = '#') - cat('Genodata:', toskip, " ", dim(genodata), genocodes, '\n') - if(is.null(phenotype)) phenotype <- runif((ncol(genodata)-4)) # If there isn't a phenotype, generate a random one - if(is.null(sex)) sex <- rep('m', (ncol(genodata)-4)) # If there isn't a sex phenotype, treat all as males - outCSVR <- rbind(c('Pheno', '', '', phenotype), # Phenotype - c('sex', '', '', sex), # Sex phenotype for the mice - cbind(genodata[,c('Locus','Chr', 'cM')], genodata[, 5:ncol(genodata)])) # Genotypes - write.table(outCSVR, file = out, row.names=FALSE, col.names=FALSE,quote=FALSE, sep=',') # Save it to a file - require(qtl) - cross = read.cross(file=out, 'csvr', genotypes=genocodes) # Load the created cross file using R/qtl read.cross - if(type == 'riset') cross <- convert2riself(cross) # If its a RIL, convert to a RIL in R/qtl - return(cross) - } - """ % (self.dataset.group.name + ".geno")) - - def run_rqtl_geno(self): - self.geno_to_rqtl_function() - - ## Get pointers to some common R functions - r_library = ro.r["library"] # Map the library function - r_c = ro.r["c"] # Map the c function - r_sum = ro.r["sum"] # Map the sum function - plot = ro.r["plot"] # Map the plot function - postscript = ro.r["postscript"] # Map the postscript function - png = ro.r["png"] # Map the png function - dev_off = ro.r["dev.off"] # Map the device off function - - print(r_library("qtl")) # Load R/qtl - - ## Get pointers to some R/qtl functions - scanone = ro.r["scanone"] # Map the scanone function - scantwo = ro.r["scantwo"] # Map the scantwo function - calc_genoprob = ro.r["calc.genoprob"] # Map the calc.genoprob function - read_cross = ro.r["read.cross"] # Map the read.cross function - write_cross = ro.r["write.cross"] # Map the write.cross function - GENOtoCSVR = ro.r["GENOtoCSVR"] # Map the local GENOtoCSVR function - - crossname = self.dataset.group.name - genofilelocation = locate(crossname + ".geno", "genotype") - crossfilelocation = TMPDIR + crossname + ".cross" - - #print("Conversion of geno to cross at location:", genofilelocation, " to ", crossfilelocation) - - cross_object = GENOtoCSVR(genofilelocation, crossfilelocation) # TODO: Add the SEX if that is available - - if self.manhattan_plot: - cross_object = calc_genoprob(cross_object) - else: - cross_object = calc_genoprob(cross_object, step=1, stepwidth="max") - - cross_object = self.add_phenotype(cross_object, self.sanitize_rqtl_phenotype()) # Add the phenotype - - # for debug: write_cross(cross_object, "csvr", "test.csvr") - - # Scan for QTLs - covar = self.create_covariates(cross_object) # Create the additive covariate matrix - - if self.pair_scan: - if self.do_control == "true": # If sum(covar) > 0 we have a covariate matrix - print("Using covariate"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", addcovar = covar, model=self.model, method=self.method, n_cluster = 16) - else: - print("No covariates"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", model=self.model, method=self.method, n_cluster = 16) - - #print("Pair scan results:", result_data_frame) - - self.pair_scan_filename = webqtlUtil.genRandStr("scantwo_") + ".png" - png(file=TEMPDIR+self.pair_scan_filename) - plot(result_data_frame) - dev_off() - - return self.process_pair_scan_results(result_data_frame) - - else: - if self.do_control == "true": - print("Using covariate"); result_data_frame = scanone(cross_object, pheno = "the_pheno", addcovar = covar, model=self.model, method=self.method) - else: - print("No covariates"); result_data_frame = scanone(cross_object, pheno = "the_pheno", model=self.model, method=self.method) - - if self.num_perm > 0 and self.permCheck == "ON": # Do permutation (if requested by user) - if self.do_control == "true": - perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", addcovar = covar, n_perm = self.num_perm, model=self.model, method=self.method) - else: - perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", n_perm = self.num_perm, model=self.model, method=self.method) - - self.process_rqtl_perm_results(perm_data_frame) # Functions that sets the thresholds for the webinterface - - return self.process_rqtl_results(result_data_frame) - - def add_phenotype(self, cross, pheno_as_string): - ro.globalenv["the_cross"] = cross - ro.r('the_cross$pheno <- cbind(pull.pheno(the_cross), the_pheno = '+ pheno_as_string +')') - return ro.r["the_cross"] - - def create_covariates(self, cross): - ro.globalenv["the_cross"] = cross - ro.r('genotypes <- pull.geno(the_cross)') # Get the genotype matrix - userinputS = self.control_marker.replace(" ", "").split(",") # TODO: sanitize user input, Never Ever trust a user - covariate_names = ', '.join('"{0}"'.format(w) for w in userinputS) - #print("Marker names of selected covariates:", covariate_names) - ro.r('covnames <- c(' + covariate_names + ')') - ro.r('covInGeno <- which(covnames %in% colnames(genotypes))') - ro.r('covnames <- covnames[covInGeno]') - ro.r("cat('covnames (purged): ', covnames,'\n')") - ro.r('covariates <- genotypes[,covnames]') # Get the covariate matrix by using the marker name as index to the genotype file - #print("R/qtl matrix of covariates:", ro.r["covariates"]) - return ro.r["covariates"] - - def sanitize_rqtl_phenotype(self): - pheno_as_string = "c(" - for i, val in enumerate(self.vals): - if val == "x": - if i < (len(self.vals) - 1): - pheno_as_string += "NA," - else: - pheno_as_string += "NA" - else: - if i < (len(self.vals) - 1): - pheno_as_string += str(val) + "," - else: - pheno_as_string += str(val) - pheno_as_string += ")" - return pheno_as_string - - def process_pair_scan_results(self, result): - pair_scan_results = [] - - result = result[1] - output = [tuple([result[j][i] for j in range(result.ncol)]) for i in range(result.nrow)] - #print("R/qtl scantwo output:", output) - - for i, line in enumerate(result.iter_row()): - marker = {} - marker['name'] = result.rownames[i] - marker['chr1'] = output[i][0] - marker['Mb'] = output[i][1] - marker['chr2'] = int(output[i][2]) - pair_scan_results.append(marker) - - #print("pair_scan_results:", pair_scan_results) - - return pair_scan_results - - def process_rqtl_results(self, result): # TODO: how to make this a one liner and not copy the stuff in a loop - qtl_results = [] - - output = [tuple([result[j][i] for j in range(result.ncol)]) for i in range(result.nrow)] - #print("R/qtl scanone output:", output) - - for i, line in enumerate(result.iter_row()): - marker = {} - marker['name'] = result.rownames[i] - marker['chr'] = output[i][0] - marker['Mb'] = output[i][1] - marker['lod_score'] = output[i][2] - qtl_results.append(marker) - - return qtl_results - - def process_rqtl_perm_results(self, results): - perm_vals = [] - for line in str(results).split("\n")[1:(self.num_perm+1)]: - #print("R/qtl permutation line:", line.split()) - perm_vals.append(float(line.split()[1])) - - self.perm_output = perm_vals - self.suggestive = np.percentile(np.array(perm_vals), 67) - self.significant = np.percentile(np.array(perm_vals), 95) - - return self.suggestive, self.significant - - def run_plink(self): plink_output_filename = webqtlUtil.genRandStr("%s_%s_"%(self.dataset.group.name, self.this_trait.name)) self.gen_pheno_txt_file_plink(pheno_filename = plink_output_filename) plink_command = PLINK_COMMAND + ' --noweb --ped %s/%s.ped --no-fid --no-parents --no-sex --no-pheno --map %s/%s.map --pheno %s%s.txt --pheno-name %s --maf %s --missing-phenotype -9999 --out %s%s --assoc ' % (PLINK_PATH, self.dataset.group.name, PLINK_PATH, self.dataset.group.name, TMPDIR, plink_output_filename, self.this_trait.name, self.maf, TMPDIR, plink_output_filename) - print("plink_command:", plink_command) + logger.debug("plink_command:", plink_command) os.system(plink_command) @@ -550,11 +370,11 @@ class MarkerRegression(object): #for marker in self.dataset.group.markers.markers: # if marker['name'] not in included_markers: - # print("marker:", marker) + # logger.debug("marker:", marker) # self.dataset.group.markers.markers.remove(marker) # #del self.dataset.group.markers.markers[marker] - print("p_values:", pf(p_values)) + logger.debug("p_values:", pf(p_values)) self.dataset.group.markers.add_pvalues(p_values) @@ -821,7 +641,7 @@ class MarkerRegression(object): top_lod_scores = [] - #print("self.num_perm:", self.num_perm) + #logger.debug("self.num_perm:", self.num_perm) for permutation in range(self.num_perm): @@ -866,10 +686,10 @@ class MarkerRegression(object): if p_value < lowest_p_value: lowest_p_value = p_value - #print("lowest_p_value:", lowest_p_value) + #logger.debug("lowest_p_value:", lowest_p_value) top_lod_scores.append(-math.log10(lowest_p_value)) - #print("top_lod_scores:", top_lod_scores) + #logger.debug("top_lod_scores:", top_lod_scores) self.suggestive = np.percentile(top_lod_scores, 67) self.significant = np.percentile(top_lod_scores, 95) @@ -877,14 +697,13 @@ class MarkerRegression(object): def gen_data(self, temp_uuid): """Generates p-values for each marker""" - - print("self.vals is:", self.vals) + logger.debug("self.vals is:", self.vals) pheno_vector = np.array([(val == "x" or val == "") and np.nan or float(val) for val in self.vals]) #lmm_uuid = str(uuid.uuid4()) key = "pylmm:input:" + temp_uuid - print("key is:", pf(key)) + logger.debug("key is:", pf(key)) #with Bench("Loading cache"): # result = Redis.get(key) @@ -893,7 +712,7 @@ class MarkerRegression(object): #p_values = self.trim_results(p_values) else: - print("NOW CWD IS:", os.getcwd()) + logger.debug("NOW CWD IS:", os.getcwd()) genotype_data = [marker['genotypes'] for marker in self.dataset.group.markers.markers] no_val_samples = self.identify_empty_samples() @@ -901,9 +720,9 @@ class MarkerRegression(object): genotype_matrix = np.array(genotype_data).T - #print("pheno_vector: ", pf(pheno_vector)) - #print("genotype_matrix: ", pf(genotype_matrix)) - #print("genotype_matrix.shape: ", pf(genotype_matrix.shape)) + #logger.debug("pheno_vector: ", pf(pheno_vector)) + #logger.debug("genotype_matrix: ", pf(genotype_matrix)) + #logger.debug("genotype_matrix.shape: ", pf(genotype_matrix.shape)) #params = {"pheno_vector": pheno_vector, # "genotype_matrix": genotype_matrix, @@ -911,8 +730,8 @@ class MarkerRegression(object): # "refit": False, # "temp_data": tempdata} - # print("genotype_matrix:", str(genotype_matrix.tolist())) - # print("pheno_vector:", str(pheno_vector.tolist())) + # logger.debug("genotype_matrix:", str(genotype_matrix.tolist())) + # logger.debug("pheno_vector:", str(pheno_vector.tolist())) params = dict(pheno_vector = pheno_vector.tolist(), genotype_matrix = genotype_matrix.tolist(), @@ -925,14 +744,14 @@ class MarkerRegression(object): ) json_params = json.dumps(params) - #print("json_params:", json_params) + #logger.debug("json_params:", json_params) Redis.set(key, json_params) Redis.expire(key, 60*60) - print("before printing command") + logger.debug("before printing command") command = PYLMM_COMMAND + ' --key {} --species {}'.format(key, "other") - print("command is:", command) - print("after printing command") + logger.debug("command is:", command) + logger.debug("after printing command") shell(command) @@ -942,7 +761,7 @@ 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]) + #logger.debug("p_values:", p_values[:10]) #p_values = self.trim_results(p_values) t_stats = results['t_stats'] @@ -953,7 +772,7 @@ class MarkerRegression(object): # refit=False, # temp_data=tempdata #) - #print("p_values:", p_values) + #logger.debug("p_values:", p_values) self.dataset.group.markers.add_pvalues(p_values) @@ -962,7 +781,7 @@ class MarkerRegression(object): return self.dataset.group.markers.markers def trim_results(self, p_values): - print("len_p_values:", len(p_values)) + logger.debug("len_p_values:", len(p_values)) if len(p_values) > 500: p_values.sort(reverse=True) trimmed_values = p_values[:500] @@ -981,7 +800,7 @@ class MarkerRegression(object): kinship_matrix = np.fromfile(open(file_base + '.kin','r'),sep=" ") kinship_matrix.resize((len(plink_input.indivs),len(plink_input.indivs))) - print("Before creating params") + logger.debug("Before creating params") params = dict(pheno_vector = pheno_vector.tolist(), covariate_matrix = covariate_matrix.tolist(), @@ -994,18 +813,18 @@ class MarkerRegression(object): timestamp = datetime.datetime.now().isoformat(), ) - print("After creating params") + logger.debug("After creating params") json_params = json.dumps(params) Redis.set(key, json_params) Redis.expire(key, 60*60) - print("Before creating the command") + logger.debug("Before creating the command") command = PYLMM_COMMAND+' --key {} --species {}'.format(key, "human") - print("command is:", command) + logger.debug("command is:", command) os.system(command) @@ -1028,7 +847,7 @@ class MarkerRegression(object): return p_values, t_stats def get_lod_score_cutoff(self): - print("INSIDE GET LOD CUTOFF") + logger.debug("INSIDE GET LOD CUTOFF") high_qtl_count = 0 for marker in self.dataset.group.markers.markers: if marker['lod_score'] > 1: diff --git a/wqflask/wqflask/marker_regression/marker_regression_gn1.py b/wqflask/wqflask/marker_regression/marker_regression_gn1.py index 9cef3cec..bc147f75 100644 --- a/wqflask/wqflask/marker_regression/marker_regression_gn1.py +++ b/wqflask/wqflask/marker_regression/marker_regression_gn1.py @@ -44,6 +44,9 @@ from utility import Plot from wqflask.interval_analyst import GeneUtil from base.webqtlConfig import TMPDIR, GENERATED_TEXT_DIR, GENERATED_IMAGE_DIR +import utility.logger +logger = utility.logger.getLogger(__name__ ) + ######################################### # Inteval Mapping Plot Page ######################################### @@ -159,6 +162,7 @@ class MarkerRegression(object): #if not self.openMysql(): # return + logger.info("Running qtlreaper") #helper_functions.get_species_dataset_trait(self, start_vars) @@ -211,7 +215,7 @@ class MarkerRegression(object): self.plotScale = start_vars['mapping_scale'] else: self.plotScale = "physic" - + self.manhattan_plot = start_vars['manhattan_plot'] if 'permCheck' in start_vars.keys(): @@ -514,13 +518,13 @@ class MarkerRegression(object): if self.dataset.group.species == "mouse": if self.selectedChr == 20: - chrName = "X" + chrName = "X" else: chrName = self.selectedChr self.geneCol = GeneUtil.loadGenes(chrName, self.diffCol, self.startMb, self.endMb, webqtldatabase, "mouse") elif self.dataset.group.species == "rat": if self.selectedChr == 21: - chrName = "X" + chrName = "X" else: chrName = self.selectedChr self.geneCol = GeneUtil.loadGenes(chrName, self.diffCol, self.startMb, self.endMb, webqtldatabase, "rat") @@ -860,7 +864,7 @@ class MarkerRegression(object): BootCoord = [] i = 0 startX = xLeftOffset - + if self.selectedChr == -1: #ZS: If viewing full genome/all chromosomes for j, _chr in enumerate(self.genotype): BootCoord.append( []) @@ -883,8 +887,8 @@ class MarkerRegression(object): else: Xc = startX + (_locus.cM-_chr[0].cM)*plotXScale BootCoord[-1].append([Xc, self.bootResult[i]]) - i += 1 - + i += 1 + #reduce bootResult if self.selectedChr > -1: maxBootBar = 80.0 @@ -1851,7 +1855,7 @@ class MarkerRegression(object): if j == 0: canvas.drawLine(startPosX,yZero,startPosX,yZero+40, color=lineColor) startPosX += (self.ChrLengthDistList[j]+self.GraphInterval)*plotXScale - + centimorganLabelFont = pid.Font(ttf="verdana", size=18*zoom*1.5, bold=0) canvas.drawString("Centimorgans", xLeftOffset + (plotWidth - canvas.stringWidth("Megabases", font=centimorganLabelFont))/2, strYLoc + canvas.fontHeight(MBLabelFont)+ 10*(zoom%2) + 10, font=centimorganLabelFont, color=pid.black) @@ -2963,7 +2967,7 @@ class MarkerRegression(object): chr_as_int = 20 else: chr_as_int = int(theGO["Chromosome"]) - 1 - + 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)) geneLengthURL = "javascript:rangeView('%s', %f, %f)" % (theGO["Chromosome"], float(theGO["TxStart"])-(geneLength*0.1), float(theGO["TxEnd"])+(geneLength*0.1)) diff --git a/wqflask/wqflask/marker_regression/rqtl_mapping.py b/wqflask/wqflask/marker_regression/rqtl_mapping.py new file mode 100644 index 00000000..93bf717c --- /dev/null +++ b/wqflask/wqflask/marker_regression/rqtl_mapping.py @@ -0,0 +1,193 @@ +import rpy2.robjects as ro
+import numpy as np
+
+from base.webqtlConfig import TMPDIR
+from utility import webqtlUtil
+from utility.tools import locate, TEMPDIR
+
+def run_rqtl_geno(vals, dataset, method, model, permCheck, num_perm, do_control, control_marker, manhattan_plot, pair_scan):
+ geno_to_rqtl_function(dataset)
+
+ ## Get pointers to some common R functions
+ r_library = ro.r["library"] # Map the library function
+ r_c = ro.r["c"] # Map the c function
+ r_sum = ro.r["sum"] # Map the sum function
+ plot = ro.r["plot"] # Map the plot function
+ postscript = ro.r["postscript"] # Map the postscript function
+ png = ro.r["png"] # Map the png function
+ dev_off = ro.r["dev.off"] # Map the device off function
+
+ print(r_library("qtl")) # Load R/qtl
+
+ ## Get pointers to some R/qtl functions
+ scanone = ro.r["scanone"] # Map the scanone function
+ scantwo = ro.r["scantwo"] # Map the scantwo function
+ calc_genoprob = ro.r["calc.genoprob"] # Map the calc.genoprob function
+ read_cross = ro.r["read.cross"] # Map the read.cross function
+ write_cross = ro.r["write.cross"] # Map the write.cross function
+ GENOtoCSVR = ro.r["GENOtoCSVR"] # Map the local GENOtoCSVR function
+
+ crossname = dataset.group.name
+ genofilelocation = locate(crossname + ".geno", "genotype")
+ crossfilelocation = TMPDIR + crossname + ".cross"
+
+ #print("Conversion of geno to cross at location:", genofilelocation, " to ", crossfilelocation)
+
+ cross_object = GENOtoCSVR(genofilelocation, crossfilelocation) # TODO: Add the SEX if that is available
+
+ if manhattan_plot:
+ cross_object = calc_genoprob(cross_object)
+ else:
+ cross_object = calc_genoprob(cross_object, step=1, stepwidth="max")
+
+ cross_object = add_phenotype(cross_object, sanitize_rqtl_phenotype(vals)) # Add the phenotype
+
+ # for debug: write_cross(cross_object, "csvr", "test.csvr")
+
+ # Scan for QTLs
+ covar = create_covariates(control_marker, cross_object) # Create the additive covariate matrix
+
+ if pair_scan:
+ if do_control == "true": # If sum(covar) > 0 we have a covariate matrix
+ print("Using covariate"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", addcovar = covar, model=model, method=method, n_cluster = 16)
+ else:
+ print("No covariates"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", model=model, method=method, n_cluster = 16)
+
+ #print("Pair scan results:", result_data_frame)
+
+ pair_scan_filename = webqtlUtil.genRandStr("scantwo_") + ".png"
+ png(file=TEMPDIR+pair_scan_filename)
+ plot(result_data_frame)
+ dev_off()
+
+ return process_pair_scan_results(result_data_frame)
+ else:
+ if do_control == "true":
+ print("Using covariate"); result_data_frame = scanone(cross_object, pheno = "the_pheno", addcovar = covar, model=model, method=method)
+ else:
+ print("No covariates"); result_data_frame = scanone(cross_object, pheno = "the_pheno", model=model, method=method)
+
+ if num_perm > 0 and permCheck == "ON": # Do permutation (if requested by user)
+ if do_control == "true":
+ perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", addcovar = covar, n_perm = num_perm, model=model, method=method)
+ else:
+ perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", n_perm = num_perm, model=model, method=method)
+
+ perm_output, suggestive, significant = process_rqtl_perm_results(num_perm, perm_data_frame) # Functions that sets the thresholds for the webinterface
+ return perm_output, suggestive, significant, process_rqtl_results(result_data_frame)
+ else:
+ return process_rqtl_results(result_data_frame)
+
+def geno_to_rqtl_function(dataset): # TODO: Need to figure out why some genofiles have the wrong format and don't convert properly
+
+ ro.r("""
+ trim <- function( x ) { gsub("(^[[:space:]]+|[[:space:]]+$)", "", x) }
+
+ getGenoCode <- function(header, name = 'unk'){
+ mat = which(unlist(lapply(header,function(x){ length(grep(paste('@',name,sep=''), x)) })) == 1)
+ return(trim(strsplit(header[mat],':')[[1]][2]))
+ }
+
+ GENOtoCSVR <- function(genotypes = '%s', out = 'cross.csvr', phenotype = NULL, sex = NULL, verbose = FALSE){
+ header = readLines(genotypes, 40) # Assume a geno header is not longer than 40 lines
+ toskip = which(unlist(lapply(header, function(x){ length(grep("Chr\t", x)) })) == 1)-1 # Major hack to skip the geno headers
+
+ genocodes <- c(getGenoCode(header, 'mat'), getGenoCode(header, 'het'), getGenoCode(header, 'pat')) # Get the genotype codes
+ type <- getGenoCode(header, 'type')
+ genodata <- read.csv(genotypes, sep='\t', skip=toskip, header=TRUE, na.strings=getGenoCode(header,'unk'), colClasses='character', comment.char = '#')
+ cat('Genodata:', toskip, " ", dim(genodata), genocodes, '\n')
+ if(is.null(phenotype)) phenotype <- runif((ncol(genodata)-4)) # If there isn't a phenotype, generate a random one
+ if(is.null(sex)) sex <- rep('m', (ncol(genodata)-4)) # If there isn't a sex phenotype, treat all as males
+ outCSVR <- rbind(c('Pheno', '', '', phenotype), # Phenotype
+ c('sex', '', '', sex), # Sex phenotype for the mice
+ cbind(genodata[,c('Locus','Chr', 'cM')], genodata[, 5:ncol(genodata)])) # Genotypes
+ write.table(outCSVR, file = out, row.names=FALSE, col.names=FALSE,quote=FALSE, sep=',') # Save it to a file
+ require(qtl)
+ cross = read.cross(file=out, 'csvr', genotypes=genocodes) # Load the created cross file using R/qtl read.cross
+ if(type == 'riset') cross <- convert2riself(cross) # If its a RIL, convert to a RIL in R/qtl
+ return(cross)
+ }
+ """ % (dataset.group.name + ".geno"))
+
+def add_phenotype(cross, pheno_as_string):
+ ro.globalenv["the_cross"] = cross
+ ro.r('the_cross$pheno <- cbind(pull.pheno(the_cross), the_pheno = '+ pheno_as_string +')')
+ return ro.r["the_cross"]
+
+def create_covariates(control_marker, cross):
+ ro.globalenv["the_cross"] = cross
+ ro.r('genotypes <- pull.geno(the_cross)') # Get the genotype matrix
+ userinputS = control_marker.replace(" ", "").split(",") # TODO: sanitize user input, Never Ever trust a user
+ covariate_names = ', '.join('"{0}"'.format(w) for w in userinputS)
+ #print("Marker names of selected covariates:", covariate_names)
+ ro.r('covnames <- c(' + covariate_names + ')')
+ ro.r('covInGeno <- which(covnames %in% colnames(genotypes))')
+ ro.r('covnames <- covnames[covInGeno]')
+ ro.r("cat('covnames (purged): ', covnames,'\n')")
+ ro.r('covariates <- genotypes[,covnames]') # Get the covariate matrix by using the marker name as index to the genotype file
+ #print("R/qtl matrix of covariates:", ro.r["covariates"])
+ return ro.r["covariates"]
+
+def sanitize_rqtl_phenotype(vals):
+ pheno_as_string = "c("
+ for i, val in enumerate(vals):
+ if val == "x":
+ if i < (len(vals) - 1):
+ pheno_as_string += "NA,"
+ else:
+ pheno_as_string += "NA"
+ else:
+ if i < (len(vals) - 1):
+ pheno_as_string += str(val) + ","
+ else:
+ pheno_as_string += str(val)
+ pheno_as_string += ")"
+ return pheno_as_string
+
+def process_pair_scan_results(result):
+ pair_scan_results = []
+
+ result = result[1]
+ output = [tuple([result[j][i] for j in range(result.ncol)]) for i in range(result.nrow)]
+ #print("R/qtl scantwo output:", output)
+
+ for i, line in enumerate(result.iter_row()):
+ marker = {}
+ marker['name'] = result.rownames[i]
+ marker['chr1'] = output[i][0]
+ marker['Mb'] = output[i][1]
+ marker['chr2'] = int(output[i][2])
+ pair_scan_results.append(marker)
+
+ #print("pair_scan_results:", pair_scan_results)
+
+ return pair_scan_results
+
+def process_rqtl_perm_results(num_perm, results):
+ perm_vals = []
+ for line in str(results).split("\n")[1:(num_perm+1)]:
+ #print("R/qtl permutation line:", line.split())
+ perm_vals.append(float(line.split()[1]))
+
+ perm_output = perm_vals
+ suggestive = np.percentile(np.array(perm_vals), 67)
+ significant = np.percentile(np.array(perm_vals), 95)
+ print("SIGNIFICANT:", significant)
+
+ return perm_output, suggestive, significant
+
+def process_rqtl_results(result): # TODO: how to make this a one liner and not copy the stuff in a loop
+ qtl_results = []
+
+ output = [tuple([result[j][i] for j in range(result.ncol)]) for i in range(result.nrow)]
+ #print("R/qtl scanone output:", output)
+
+ for i, line in enumerate(result.iter_row()):
+ marker = {}
+ marker['name'] = result.rownames[i]
+ marker['chr'] = output[i][0]
+ marker['Mb'] = output[i][1]
+ marker['lod_score'] = output[i][2]
+ qtl_results.append(marker)
+
+ return qtl_results
\ No newline at end of file diff --git a/wqflask/wqflask/show_trait/show_trait.py b/wqflask/wqflask/show_trait/show_trait.py index 912beabe..d9617c7c 100644 --- a/wqflask/wqflask/show_trait/show_trait.py +++ b/wqflask/wqflask/show_trait/show_trait.py @@ -23,8 +23,7 @@ from basicStatistics import BasicStatisticsFunctions from pprint import pformat as pf -from utility.tools import flat_files -MAPPING_PATH = flat_files("mapping") +from utility.tools import flat_files, flat_file_exists from utility.logger import getLogger logger = getLogger(__name__ ) @@ -163,11 +162,12 @@ class ShowTrait(object): def get_mapping_methods(self): '''Only display mapping methods when the dataset group's genotype file exists''' def check_plink_gemma(): - if (os.path.isfile(MAPPING_PATH+"/"+self.dataset.group.name+".bed") and - os.path.isfile(MAPPING_PATH+"/"+self.dataset.group.name+".map")): - return True - else: - return False + if flat_file_exists("mapping"): + MAPPING_PATH = flat_files("mapping")+"/" + if 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b/wqflask/wqflask/static/gif/error/animated-gifs-stickmen-069.gif Binary files differnew file mode 100644 index 00000000..473212e4 --- /dev/null +++ b/wqflask/wqflask/static/gif/error/animated-gifs-stickmen-069.gif diff --git a/wqflask/wqflask/templates/base.html b/wqflask/wqflask/templates/base.html index 6af07edc..c3826a90 100644 --- a/wqflask/wqflask/templates/base.html +++ b/wqflask/wqflask/templates/base.html @@ -80,9 +80,9 @@ </div> </div> </div> - + <div class="container-fluid" style="background-color: #d5d5d5; height: 95px;"> - + <form method="get" action="/gsearch"> <div class="row"> <select class="form-control col-xs-2" style="width: 170px; margin-top: 15px; margin-left: 10px;" name="type"> @@ -101,62 +101,50 @@ ================================================== --> <footer class="footer"> <div class="container"> - <p class="pull-right"><a href="#">Back to top</a></p> - <p>Launched in 1994 as - <A HREF="http://www.ncbi.nlm.nih.gov/pubmed?term=8043953"> - The Portable Dictionary of the Mouse Genome</A> and in 2001 as WebQTL. - </p> - <p>Operated by - <A HREF="mailto:rwilliams@uthsc.edu">Rob Williams</A>, - <A HREF="mailto:lyan6@uthsc.edu">Lei Yan</A>, - <A HREF="mailto:zachary.a.sloan@gmail.com">Zachary Sloan</A>, and - <A HREF="mailto:acenteno@uthsc.edu" target="_blank">Arthur Centeno</A>. - </p> <p> - Designed and coded by <a href="http://penguinpython.com">Sam Ockman</a>, Xiaodong Zhou, - Christian Fernandez, - Ning Liu, Rudi Alberts, Elissa Chesler, Jintao Wang, Kenneth Manly, Robert W. Williams, - and <A HREF="/credit.html">colleagues</A>. - </p> - <p>Built with <a href="http://twitter.github.com/bootstrap/">bootstrap</a>, - <a href="http://coffeescript.org/">coffeescript</a>, - <a href="http://flask.pocoo.org/">flask</a>, - <a href="http://en.wikipedia.org/wiki/Linux">linux</a>, - <a href="http://www.python.org/">python</a> and good intentions. +GeneNetwork is a framework for web based genetics + launched in 1994 as + <a href="http://www.ncbi.nlm.nih.gov/pubmed?term=8043953"> + The Portable Dictionary of the Mouse Genome</a> (previously <a href="https://www.ncbi.nlm.nih.gov/pubmed/15043217">WebQTL</a>). + </p> + <p>Operated by + <a href="mailto:rwilliams@uthsc.edu">Rob Williams</a>, + <a href="mailto:lyan6@uthsc.edu">Lei Yan</a>, + <a href="mailto:zachary.a.sloan@gmail.com">Zachary Sloan</a>, and + <a href="mailto:acenteno@uthsc.edu">Arthur Centeno</a>. </p> - <br /> + <p>Published in + <a href="http://joss.theoj.org/papers/10.21105/joss.00025"><img src="https://camo.githubusercontent.com/846b750f582ae8f1d0b4f7e8fee78bed705c88ba/687474703a2f2f6a6f73732e7468656f6a2e6f72672f7061706572732f31302e32313130352f6a6f73732e30303032352f7374617475732e737667" alt="JOSS" data-canonical-src="http://joss.theoj.org/papers/10.21105/joss.00025/status.svg" style="max-width:100%;"></a> + </p> + <br /> <p>GeneNetwork is supported by:</p> <UL> <LI> - <a target="_blank" href="http://citg.uthsc.edu"> + <a href="http://citg.uthsc.edu"> The UT Center for Integrative and Translational Genomics </A> </li> - <LI><a target="_blank" href="http://www.iniastress.org">NIAAA</A> + <LI><a href="http://www.iniastress.org">NIAAA</A> Integrative Neuroscience Initiative on Alcoholism (U01 AA016662, U01 AA013499, U24 AA013513, U01 AA014425) </li> <LI> - <a target="_blank" - href="http://www.drugabuse.gov/about/organization/Genetics/geneexpression/index.html">NIDA</A>, <a class="smallsize" target="_blank" href="http://www.nimh.nih.gov/">NIMH</A> - , and <a class="smallsize" target="_blank" href="http://www.niaaa.nih.gov/"> + <a + href="https://www.drugabuse.gov/">NIDA</A>, <a class="smallsize" href="http://www.nimh.nih.gov/">NIMH</A> + , and <a class="smallsize" href="http://www.niaaa.nih.gov/"> NIAAA</A> (P20-DA 21131) </li> - <LI>NCI <a target="_blank" href="http://emice.nci.nih.gov/">MMHCC</A> (U01CA105417) and - <a target="_blank" href="http://www.ncrr.nih.gov/">NCRR</A> - <a target="_blank" href="http://www.nbirn.net/TestBeds/Mouse/index.htm">BIRN</A> + <LI>NCI <a href="http://emice.nci.nih.gov/">MMHCC</A> (U01CA105417) and + <a href="https://en.wikipedia.org/wiki/National_Center_for_Research_Resources">NCRR</a> + <a href="https://en.wikipedia.org/wiki/Biomedical_Informatics_Research_Network">BIRN</a> (U24 RR021760) </li> </UL> <!--</p>--> - <ul class="footer-links"> - <li><a href="http://listserv.uthsc.edu/mailman/listinfo/genenetwork-dev">Join the mailing list</a></li> - <!--<li><a href="#">Friend us on facebook</a></li>--> - <!--<li><a href="#">Follow us on twitter</a></li>--> - </ul> + Join the <a href="http://listserv.uthsc.edu/mailman/listinfo/genenetwork-dev">mailing list</a> </div> </footer> diff --git a/wqflask/wqflask/templates/collections/add.html b/wqflask/wqflask/templates/collections/add.html index 47b87d73..d45aa015 100644 --- a/wqflask/wqflask/templates/collections/add.html +++ b/wqflask/wqflask/templates/collections/add.html @@ -25,7 +25,7 @@ <select name="existing_collection" class="form-control"> {% for col in collections %} - <option value="{{ col.id }}">{{ col.name }}</option> + <option value="{{ col.id }}:{{ col.name }}">{{ col.name }}</option> {% endfor %} </select> <br /> diff --git a/wqflask/wqflask/templates/ctl_setup.html b/wqflask/wqflask/templates/ctl_setup.html index 9c0d7bea..51553322 100644 --- a/wqflask/wqflask/templates/ctl_setup.html +++ b/wqflask/wqflask/templates/ctl_setup.html @@ -1,65 +1,70 @@ {% extends "base.html" %} -{% block title %}WCGNA analysis{% endblock %} +{% block title %}CTL analysis{% endblock %} {% block content %} <!-- Start of body --> <div class="container"> + {% if request.form['trait_list'].split(",")|length < 2 %} + <div class="alert alert-danger" role="alert"> + <span class="glyphicon glyphicon-exclamation-sign" aria-hidden="true"></span> + <span class="sr-only">Error:</span> + <h2>Too few traits as input</h2> + Please make sure you select enough traits to perform CTL. Your collection needs to contain at least 2 different traits. You provided {{request.form['trait_list'].split(',')|length}} traits as input. + </div> + {% else %} <h1>CTL analysis parameters</h1> - {{(request.form['trait_list'].split(',')|length -1)}} phenotypes as input + {{(request.form['trait_list'].split(',')|length -1)}} traits as input -<form action="/ctl_results" method="post" class="form-horizontal"> - <input type="hidden" name="trait_list" id="trait_list" value= "{{request.form['trait_list']}}"> + <form action="/ctl_results" method="post" class="form-horizontal"> + <input type="hidden" name="trait_list" id="trait_list" value= "{{request.form['trait_list']}}"> + <div class="dropdown"> + <label for="Strategy">Strategy</label> + <div class="col-sm-10"> + <select name="strategy" id="strategy"> + <option value="Exact">Exact</option> + <option value="Full">Full</option> + <option value="Pairwise">Pairwise</option> + </select> + </div> + </div> - <div class="dropdown"> - <label for="Strategy">Strategy</label> - <div class="col-sm-10"> - <select name="strategy" id="strategy"> - <option value="Exact">Exact</option> - <option value="Full">Full</option> - <option value="Pairwise">Pairwise</option> - </select> - </div> - </div> + <div class="dropdown"> + <label for="Permutations">Number of permutation (Used when strategy is Full or Pairwise)</label> + <div class="col-sm-10"> + <select name="nperm" id="nperm"> + <option value="100">100</option> + <option value="1000" selected="selected">1000</option> + <option value="10000">10000</option> + </select> + </div> + </div> - <div class="dropdown"> - <label for="Permutations">Number of permutation (Used when strategy is Full or Pairwise)</label> - <div class="col-sm-10"> - <select name="nperm" id="nperm"> - <option value="100">100</option> - <option value="1000" selected="selected">1000</option> - <option value="10000">10000</option> - </select> - </div> - </div> - - <div class="dropdown"> - <label for="Coefficient">Type of correlation coefficient</label> - <div class="col-sm-10"> - <select name="parametric" id="parametric"> - <option value="False">Spearman</option> - <option value="True">Pearson</option> - </select> - </div> - </div> - - - <div class="dropdown"> - <label for="Significance">Significance level</label> - <div class="col-sm-10"> - <select name="significance" id="significance"> - <option value="0.1">0.1</option> - <option value="0.05" selected="selected">0.05</option> - <option value="0.001">0.001</option> - </select> - </div> - </div> - <br> - <div class="form-group"> - <div class="col-sm-10"> - <input type="submit" class="btn btn-primary" value="Run CTL using these settings" /> - </div> - </div> + <div class="dropdown"> + <label for="Coefficient">Type of correlation coefficient</label> + <div class="col-sm-10"> + <select name="parametric" id="parametric"> + <option value="False">Spearman</option> + <option value="True">Pearson</option> + </select> + </div> + </div> + <div class="dropdown"> + <label for="Significance">Significance level</label> + <div class="col-sm-10"> + <select name="significance" id="significance"> + <option value="0.1">0.1</option> + <option value="0.05" selected="selected">0.05</option> + <option value="0.001">0.001</option> + </select> + </div> + </div> + <br> + <div class="form-group"> + <div class="col-sm-10"> + <input type="submit" class="btn btn-primary" value="Run CTL using these settings" /> + </div> + </div> </form> - +{% endif %} </div> {% endblock %} diff --git a/wqflask/wqflask/templates/error.html b/wqflask/wqflask/templates/error.html new file mode 100644 index 00000000..7ab2bf2f --- /dev/null +++ b/wqflask/wqflask/templates/error.html @@ -0,0 +1,61 @@ +{% extends "base.html" %} +{% block title %}Error: {{message}}{% endblock %} +{% block content %} +<!-- Start of body --> + +<div class="col-md-8"> +<div class="form-group has-error"> + <div class="control-label" for="inputError1"> + + <img src="/static/gif/error/{{ error_image }}"> + + <h1>ERROR</h1> + + <p> + This error is not what we wanted to see. Unfortunately errors + are part of all software systems and we need to resolve this + together. + </p> + <p> + <b>It is important to report this ERROR so we can fix it for everyone</b>. + </p> + + <p> + Report to the GeneNetwork team by recording the steps you take + to reproduce this ERROR. Next to those steps, copy-paste below + stack trace, either as + a <a href="https://github.com/genenetwork/genenetwork2/issues/new">new + issue</a> or E-mail this full page to one of the developers + directly. + </p> + </div> + + <p> + (GeneNetwork error: {{message[:128]}}) + </p> + + <pre> + {{ stack[0] }} + {{ message }} (error) + {{ stack[-3] }} + {{ stack[-2] }} + </pre> + + <p> + To check if this already a known issue, search the + <a href="https://github.com/genenetwork/genenetwork2/issues">issue + tracker</a>. + </p> + + <a href="#Stack" class="btn btn-default" data-toggle="collapse">Toggle full stack trace</a> + <div id="Stack" class="collapse"> + <pre> + {% for line in stack %} {{ line }} + {% endfor %} + </pre> + </div> +</div> +</div> + + +{% endblock %} diff --git a/wqflask/wqflask/templates/index_page.html b/wqflask/wqflask/templates/index_page.html index dc7e058c..3b96d1e1 100644 --- a/wqflask/wqflask/templates/index_page.html +++ b/wqflask/wqflask/templates/index_page.html @@ -72,7 +72,7 @@ </div> <!-- USER HELP --> - <!--<p >Databases marked with <b>**</b>--> + <!--<p>Databases marked with <b>**</b>--> <!-- suffix are not public yet.<br>--> <!-- Access requires <a href="/account.html" target=--> <!-- "_blank" class="fs14">user login</a>.</p>--> @@ -140,27 +140,26 @@ chromosome 1 between 25 and 30 Mb.</li> <li><b>MEAN=(15 16) LRS=(23 46)</b> in the <b>Combined</b> field finds - highly expressed genes (15 to 16 log2 units) AND with peak <a href="http://www.genenetwork.org/glossary.html#L" target="_blank">LRS</a> + highly expressed genes (15 to 16 log2 units) AND with peak <a href="http://www.genenetwork.org/glossary.html#L">LRS</a> linkage between 23 and 46.</li> - <li><b>RIF=mitochondrial</b> searches RNA databases for <a href="https://en.wikipedia.org/wiki/GeneRIF" target="_blank"> + <li><b>RIF=mitochondrial</b> searches RNA databases for <a href="https://en.wikipedia.org/wiki/GeneRIF"> GeneRIF</a> links.</li> - <li><b>WIKI=nicotine</b> searches <a href="http://www.genenetwork.org/webqtl/main.py?FormID=geneWiki" target="_blank"> + <li><b>WIKI=nicotine</b> searches <a href="http://www.genenetwork.org/webqtl/main.py?FormID=geneWiki"> GeneWiki</a> for genes that you or other users have annotated with the word <i>nicotine</i>.</li> <li><b>GO:0045202</b> searches for synapse-associated genes listed in the - <a href="http://www.godatabase.org/cgi-bin/amigo/go.cgi" target="_blank"> - Gene Ontology</a>.</li> + <a href="http://amigo.geneontology.org/amigo/medial_search?q=GO%3A0045202">Gene Ontology</a>.</li> <li><b>GO:0045202 LRS=(9 99 Chr4 122 155) cisLRS=(9 999 10)</b> - finds synapse-associated genes with <a href="http://www.genenetwork.org/glossary.html#E" target="_blank"> + finds synapse-associated genes with <a href="http://www.genenetwork.org/glossary.html#E"> cis eQTL</a> on Chr 4 from 122 and 155 Mb with LRS scores between 9 and 999.</li> <li><b>RIF=diabetes LRS=(9 999 Chr2 100 105) transLRS=(9 999 10)</b> - finds diabetes-associated transcripts with peak <a href="http://www.genenetwork.org/glossary.html#E" target="_blank"> + finds diabetes-associated transcripts with peak <a href="http://www.genenetwork.org/glossary.html#E"> trans eQTLs</a> on Chr 2 between 100 and 105 Mb with LRS scores between 9 and 999.</li> </ul> @@ -176,7 +175,7 @@ <h3>Thirty minute tour</h3> <p> Take the 30 minute - GeneNetwork <a href="http://www.genenetwork.org/tutorial/WebQTLTour/" target="_blank" class="fs14">tour</a> that includes screen shots and + GeneNetwork <a href="http://www.genenetwork.org/tutorial/WebQTLTour/" class="fs14">tour</a> that includes screen shots and typical steps in the analysis. </p> @@ -187,8 +186,8 @@ and Database fields above. </p> - <p>The <a href="/conditionsofUse.html" target="_blank">conditions</a> - and <a href="/statusandContact.html" target="_blank">contact + <p>The <a href="/conditionsofUse.html">conditions</a> + and <a href="/statusandContact.html">contact </a> pages have information on the status of data sets and advice on their use and citation.</p> @@ -201,25 +200,25 @@ </div> <h3>Websites affiliated with GeneNetwork</h3> <ul> - <li><a href="http://ucscbrowser.genenetwork.org/" target="_blank">Genome + <li><a href="http://ucscbrowser.genenetwork.org/">Genome browser</a> at UTHSC</li> - <li><a href="http://galaxy.genenetwork.org/" target="_blank">Galaxy</a> at + <li><a href="http://galaxy.genenetwork.org/">Galaxy</a> at UTHSC</li> - <li>GeneNetwork 1 at <a href="http://ec2.genenetwork.org/" target="_blank">Amazon + <li>GeneNetwork 1 at <a href="http://ec2.genenetwork.org/">Amazon Cloud (EC2)</a></li> - <li>GeneNetwork 1 Source Code at <a href="http://sourceforge.net/projects/genenetwork/" target="_blank">SourceForge</a></li> + <li>GeneNetwork 1 Source Code at <a href="http://sourceforge.net/projects/genenetwork/">SourceForge</a></li> - <li>GeneNetwork 2 Source Code at <a href="https://github.com/genenetwork/genenetwork2" target="_blank">GitHub</a></li> + <li>GeneNetwork 2 Source Code at <a href="https://github.com/genenetwork/genenetwork2">GitHub</a></li> </ul> <h3>GN1 Mirror and development sites</h3> <ul> - <li><a href="http://www.genenetwork.org/" target="_blank">Main GN1 site at UTHSC</a> (main site)</li> - <li><a href="http://genenetwork.helmholtz-hzi.de/" target="_blank">Germany at the HZI</a></li> - <li><a href="http://genenetwork.memphis.edu/" target="_blank">Memphis at the U of M</a></li> + <li><a href="http://www.genenetwork.org/">Main GN1 site at UTHSC</a> (main site)</li> + <li><a href="http://genenetwork.helmholtz-hzi.de/">Germany at the HZI</a></li> + <li><a href="http://gn2.genenetwork.org/">Memphis at the U of M</a></li> </ul> </section> @@ -256,7 +255,7 @@ <h3>User Guide</h3> <h5>Read the - <a href="http://www.genenetwork.org/index4.html" target="_blank"> + <a href="http://www.genenetwork.org/index4.html"> user guide</a>.</h5> </section>--> diff --git a/wqflask/wqflask/templates/index_page_orig.html b/wqflask/wqflask/templates/index_page_orig.html index 9fba0e31..73d3e718 100755 --- a/wqflask/wqflask/templates/index_page_orig.html +++ b/wqflask/wqflask/templates/index_page_orig.html @@ -7,15 +7,15 @@ <header class="jumbotron subhead" id="overview"> <div class="container"> <h1>GeneNetwork</h1> - <p class="lead">Open source bioinformatics for systems genetics</p> + <p class="lead">Open source bioinformatics for systems genetics</p> </div> </header> --> <div class="container-fluid"> - + {{ flash_me() }} - + <div class="row" style="width: 1400px !important;"> <div class="col-xs-5"> @@ -90,7 +90,7 @@ <!-- GET ANY HELP --> <div class="form-group"> <label for="btsearch" class="col-xs-1 control-label" style="width: 65px !important;"></label> - <div class="col-xs-10 controls"> + <div class="col-xs-10 controls"> <div class="col-xs-12 controls"> Enter terms, genes, ID numbers in the <b>Search</b> field.<br> Use <b>*</b> or <b>?</b> wildcards (Cyp*a?, synap*).<br> @@ -113,7 +113,7 @@ <div class="col-xs-10 controls"> <div class="col-xs-2 controls" style="width: 100px !important;"> <input id="btsearch" type="submit" class="btn btn-primary form-control" value="Search"> - </div> + </div> </div> </div> @@ -140,27 +140,27 @@ chromosome 1 between 25 and 30 Mb.</li> <li><b>MEAN=(15 16) LRS=(23 46)</b> in the <b>Combined</b> field finds - highly expressed genes (15 to 16 log2 units) AND with peak <a href="http://www.genenetwork.org/glossary.html#L" target="_blank">LRS</a> + highly expressed genes (15 to 16 log2 units) AND with peak <a href="http://www.genenetwork.org/glossary.html#L">LRS</a> linkage between 23 and 46.</li> - <li><b>RIF=mitochondrial</b> searches RNA databases for <a href="https://en.wikipedia.org/wiki/GeneRIF" target="_blank"> + <li><b>RIF=mitochondrial</b> searches RNA databases for <a href="https://en.wikipedia.org/wiki/GeneRIF"> GeneRIF</a> links.</li> - <li><b>WIKI=nicotine</b> searches <a href="http://www.genenetwork.org/webqtl/main.py?FormID=geneWiki" target="_blank"> + <li><b>WIKI=nicotine</b> searches <a href="http://www.genenetwork.org/webqtl/main.py?FormID=geneWiki"> GeneWiki</a> for genes that you or other users have annotated with the word <i>nicotine</i>.</li> <li><b>GO:0045202</b> searches for synapse-associated genes listed in the - <a href="http://www.godatabase.org/cgi-bin/amigo/go.cgi" target="_blank"> + <a href="http://amigo.geneontology.org/amigo/medial_search?q=GO%3A0045202"> Gene Ontology</a>.</li> <li><b>GO:0045202 LRS=(9 99 Chr4 122 155) cisLRS=(9 999 10)</b> - finds synapse-associated genes with <a href="http://www.genenetwork.org/glossary.html#E" target="_blank"> + finds synapse-associated genes with <a href="http://www.genenetwork.org/glossary.html#E"> cis eQTL</a> on Chr 4 from 122 and 155 Mb with LRS scores between 9 and 999.</li> <li><b>RIF=diabetes LRS=(9 999 Chr2 100 105) transLRS=(9 999 10)</b> - finds diabetes-associated transcripts with peak <a href="http://www.genenetwork.org/glossary.html#E" target="_blank"> + finds diabetes-associated transcripts with peak <a href="http://www.genenetwork.org/glossary.html#E"> trans eQTLs</a> on Chr 2 between 100 and 105 Mb with LRS scores between 9 and 999.</li> </ul> @@ -176,7 +176,7 @@ <h3>Thirty minute tour</h3> <p> Take the 30 minute - GeneNetwork <a href="http://www.genenetwork.org/tutorial/WebQTLTour/" target="_blank" class="fs14">tour</a> that includes screen shots and + GeneNetwork <a href="http://www.genenetwork.org/tutorial/WebQTLTour/" class="fs14">tour</a> that includes screen shots and typical steps in the analysis. </p> @@ -187,8 +187,8 @@ and Database fields above. </p> - <p>The <a href="/conditionsofUse.html" target="_blank">conditions</a> - and <a href="/statusandContact.html" target="_blank">contact + <p>The <a href="/conditionsofUse.html">conditions</a> + and <a href="/statusandContact.html">contact </a> pages have information on the status of data sets and advice on their use and citation.</p> @@ -201,25 +201,25 @@ </div> <h3>Websites affiliated with GeneNetwork</h3> <ul> - <li><a href="http://ucscbrowser.genenetwork.org/" target="_blank">Genome + <li><a href="http://ucscbrowser.genenetwork.org/">Genome browser</a> at UTHSC</li> - <li><a href="http://galaxy.genenetwork.org/" target="_blank">Galaxy</a> at + <li><a href="http://galaxy.genenetwork.org/">Galaxy</a> at UTHSC</li> - <li>GeneNetwork 1 at <a href="http://ec2.genenetwork.org/" target="_blank">Amazon + <li>GeneNetwork 1 at <a href="http://ec2.genenetwork.org/">Amazon Cloud (EC2)</a></li> - <li>GeneNetwork 1 Source Code at <a href="http://sourceforge.net/projects/genenetwork/" target="_blank">SourceForge</a></li> + <li>GeneNetwork 1 Source Code at <a href="http://sourceforge.net/projects/genenetwork/">SourceForge</a></li> - <li>GeneNetwork 2 Source Code at <a href="https://github.com/genenetwork/genenetwork2" target="_blank">GitHub</a></li> + <li>GeneNetwork 2 Source Code at <a href="https://github.com/genenetwork/genenetwork2">GitHub</a></li> </ul> <h3>GN1 Mirror and development sites</h3> <ul> - <li><a href="http://www.genenetwork.org/" target="_blank">Main GN1 site at UTHSC</a> (main site)</li> - <li><a href="http://genenetwork.helmholtz-hzi.de/" target="_blank">Germany at the HZI</a></li> - <li><a href="http://genenetwork.memphis.edu/" target="_blank">Memphis at the U of M</a></li> + <li><a href="http://www.genenetwork.org/">Main GN1 site at UTHSC</a> (main site)</li> + <li><a href="http://genenetwork.helmholtz-hzi.de/">Germany at the HZI</a></li> + <li><a href="http://gn2.genenetwork.org/">Memphis at the U of M</a></li> </ul> </section> @@ -256,7 +256,7 @@ <h3>User Guide</h3> <h5>Read the - <a href="http://www.genenetwork.org/index4.html" target="_blank"> + <a href="http://www.genenetwork.org/index4.html"> user guide</a>.</h5> </section>--> @@ -272,10 +272,10 @@ <script> function pressed(e) { // Has the enter key been pressed? - if ( (window.event ? event.keyCode : e.which) == 13) { + if ( (window.event ? event.keyCode : e.which) == 13) { // If enter key has been pressed and the search fields are non-empty - // manually submit the <form> - if( event.target.value.trim() != "" ) { + // manually submit the <form> + if( event.target.value.trim() != "" ) { document.forms[1].submit(); } } diff --git a/wqflask/wqflask/templates/show_trait_mapping_tools.html b/wqflask/wqflask/templates/show_trait_mapping_tools.html index 3d9c2521..0f293942 100644 --- a/wqflask/wqflask/templates/show_trait_mapping_tools.html +++ b/wqflask/wqflask/templates/show_trait_mapping_tools.html @@ -2,7 +2,7 @@ {% if (use_pylmm_rqtl and dataset.group.species != "human") or use_plink_gemma %} <div class="col-xs-4"> <div class="tabbable"> <!-- Only required for left/right tabs --> - + <ul class="nav nav-pills"> {% if use_pylmm_rqtl and not use_plink_gemma and dataset.group.species != "human" %} <li class="active"> @@ -61,7 +61,7 @@ No </label> </div> - </div> + </div> <!-- <div class="mapping_method_fields form-group"> @@ -75,7 +75,7 @@ <div class="mapping_method_fields form-group"> <label style="text-align:left;" class="col-xs-12 control-label">Display Additive Effect</label> - <div class="col-xs-12 controls" id="display_additive_effect"> + <div class="col-xs-12 controls" id="display_additive_effect"> <label class="radio-inline"> <input type="radio" name="display_additive" id="display_additive" value="yes" checked=""> Yes @@ -90,8 +90,8 @@ <div class="mapping_method_fields form-group"> - <label style="text-align:left;" class="col-xs-12 control-label">Marker Regr.</label> - <div class="col-xs-12 controls"> + <label style="text-align:left;" class="col-xs-3 control-label">Marker<br>Regression</label> + <div style="margin-left: 20px;" class="col-xs-4 controls"> <label class="radio-inline"> <input type="radio" name="manhattan_plot_reaper" value="True"> Yes @@ -146,7 +146,7 @@ <div class="mapping_method_fields form-group"> <label style="text-align:left;" class="col-xs-12 control-label">Manhattan Plot</label> - <div class="col-xs-12 controls"> + <div class="col-xs-12 controls"> <label class="radio-inline"> <input type="radio" name="manhattan_plot_pylmm" value="True"> Yes @@ -167,7 +167,7 @@ </div> </div> <div class="tab-pane" id="rqtl_geno"> - + <div style="margin-top: 20px" class="form-horizontal"> <div class="mapping_method_fields form-group"> <label for="mapping_permutations" class="col-xs-3 control-label">Permutations</label> @@ -226,7 +226,7 @@ <div class="mapping_method_fields form-group"> <label style="text-align:left;" class="col-xs-12 control-label">Pair Scan</label> - <div class="col-xs-12 controls"> + <div class="col-xs-12 controls"> <label class="radio-inline"> <input type="radio" name="pair_scan" value="true"> Yes @@ -240,7 +240,7 @@ <div class="mapping_method_fields form-group"> <label style="text-align:left;" class="col-xs-12 control-label">Manhattan Plot</label> - <div class="col-xs-12 controls"> + <div class="col-xs-12 controls"> <label class="radio-inline"> <input type="radio" name="manhattan_plot_rqtl" value="True"> Yes @@ -272,7 +272,7 @@ </div> </div> </div> - + <div class="form-group"> <label for="plink_compute" class="col-xs-1 control-label"></label> <div style="margin-left:20px;" class="col-xs-4 controls"> @@ -282,7 +282,7 @@ </div> </div> </div> - + <div class="tab-pane" id="gemma"> <div style="padding: 20px" class="form-horizontal"> <div class="mapping_method_fields form-group"> @@ -292,7 +292,7 @@ </div> </div> </div> - + <div class="form-group"> <label for="gemma_compute" class="col-xs-1 control-label"></label> <div style="margin-left:20px;" class="col-xs-4 controls"> @@ -301,12 +301,12 @@ </button> </div> </div> - </div> + </div> {% endif %} </div> </div> </div> - <div class="col-xs-6"> + <div class="col-xs-6"> <dl> <dt>Interval Mapping</dt> <dd>Interval mapping is a process in which the statistical significance of a hypothetical QTL is evaluated at regular points across a chromosome, even in the absence of explicit genotype data at those points.</dd> diff --git a/wqflask/wqflask/templates/wgcna_setup.html b/wqflask/wqflask/templates/wgcna_setup.html index b4a5730d..c5461497 100644 --- a/wqflask/wqflask/templates/wgcna_setup.html +++ b/wqflask/wqflask/templates/wgcna_setup.html @@ -4,49 +4,46 @@ {% block content %} <!-- Start of body --> <h1> WGCNA analysis parameters</h1> <div class="container"> - {% if request.form['trait_list'].split(",")|length <= 4 %} - - <div class="alert alert-danger" role="alert"> - <span class="glyphicon glyphicon-exclamation-sign" aria-hidden="true"></span> - <span class="sr-only">Error:</span> - <h2> - Too few phenotypes as input - </h2> - Please make sure you select enough phenotypes / genes to perform WGCNA, your collection needs to contain at least 4 different phenotypes. You provided {{request.form['trait_list'].split(',')|length}} phenotypes as input - </div> - {% else %} - <form action="/wgcna_results" method="post" class="form-horizontal"> - <input type="hidden" name="trait_list" id="trait_list" value= "{{request.form['trait_list']}}"> - <div class="form-group"> - <label for="SoftThresholds"> Soft threshold: </label> - <div class="col-sm-10"> - <input type="text" class="form-inline" name="SoftThresholds" id="SoftThresholds" value="1,2,3,4,5,6,7,8,9"> - </div> - </div> - <div class="form-group"> - <label for="MinModuleSize"> Minimum module size: </label> - <div class="col-sm-10"> - <input type="text" class="form-inline" name="MinModuleSize" id="MinModuleSize" value="30"> - </div> - </div> - <div class="form-group"> - <label for="TOMtype"> TOMtype: </label> - <div class="col-sm-10"> - <input type="text" class="form-inline" name="TOMtype" id="TOMtype" value="unsigned"> - </div> - </div> - <div class="form-group"> - <label for="mergeCutHeight"> mergeCutHeight: </label> - <div class="col-sm-10"> - <input type="text" class="form-inline" name="mergeCutHeight" id="mergeCutHeight" value="0.25"> - </div> - </div> - <div class="form-group"> - <div class="col-sm-10"> - <input type="submit" class="btn btn-primary" value="Run WGCNA using these settings" /> - </div> - </div> - </form> - {% endif %} + {% if request.form['trait_list'].split(",")|length < 4 %} + <div class="alert alert-danger" role="alert"> + <span class="glyphicon glyphicon-exclamation-sign" aria-hidden="true"></span> + <span class="sr-only">Error:</span> + <h2>Too few phenotypes as input</h2> + Please make sure you select enough phenotypes / genes to perform WGCNA. Your collection needs to contain at least 4 different phenotypes. You provided {{request.form['trait_list'].split(',')|length}} phenotypes as input. + </div> + {% else %} + <form action="/wgcna_results" method="post" class="form-horizontal"> + <input type="hidden" name="trait_list" id="trait_list" value= "{{request.form['trait_list']}}"> + <div class="form-group"> + <label for="SoftThresholds"> Soft threshold: </label> + <div class="col-sm-10"> + <input type="text" class="form-inline" name="SoftThresholds" id="SoftThresholds" value="1,2,3,4,5,6,7,8,9"> + </div> + </div> + <div class="form-group"> + <label for="MinModuleSize"> Minimum module size: </label> + <div class="col-sm-10"> + <input type="text" class="form-inline" name="MinModuleSize" id="MinModuleSize" value="30"> + </div> + </div> + <div class="form-group"> + <label for="TOMtype"> TOMtype: </label> + <div class="col-sm-10"> + <input type="text" class="form-inline" name="TOMtype" id="TOMtype" value="unsigned"> + </div> + </div> + <div class="form-group"> + <label for="mergeCutHeight"> mergeCutHeight: </label> + <div class="col-sm-10"> + <input type="text" class="form-inline" name="mergeCutHeight" id="mergeCutHeight" value="0.25"> + </div> + </div> + <div class="form-group"> + <div class="col-sm-10"> + <input type="submit" class="btn btn-primary" value="Run WGCNA using these settings" /> + </div> + </div> + </form> + {% endif %} </div> {% endblock %} diff --git a/wqflask/wqflask/views.py b/wqflask/wqflask/views.py index 08eb5ad6..8ea3f48f 100644 --- a/wqflask/wqflask/views.py +++ b/wqflask/wqflask/views.py @@ -4,6 +4,11 @@ from __future__ import absolute_import, division, print_function +import traceback # for error page +import os # for error gifs +import random # for random error gif +import datetime # for errors +import time # for errors import sys import csv import xlsxwriter @@ -27,7 +32,7 @@ import base64 import array import sqlalchemy from wqflask import app -from flask import g, Response, request, render_template, send_from_directory, jsonify, redirect +from flask import g, Response, request, make_response, render_template, send_from_directory, jsonify, redirect from wqflask import search_results from wqflask import gsearch from wqflask import update_search_results @@ -60,6 +65,8 @@ from wqflask import user_manager from wqflask import collect from wqflask.database import db_session +import werkzeug + import utility.logger logger = utility.logger.getLogger(__name__ ) @@ -84,6 +91,31 @@ def shutdown_session(exception=None): # from wqflask import tracer # tracer.turn_on() +@app.errorhandler(Exception) +def handle_bad_request(e): + err_msg = str(e) + logger.error(err_msg) + logger.error(request.url) + # get the stack trace and send it to the logger + exc_type, exc_value, exc_traceback = sys.exc_info() + logger.error(traceback.format_exc()) + now = datetime.datetime.utcnow() + time_str = now.strftime('%l:%M%p UTC %b %d, %Y') + formatted_lines = [request.url + " ("+time_str+")"]+traceback.format_exc().splitlines() + + # Handle random animations + # Use a cookie to have one animation on refresh + animation = request.cookies.get(err_msg[:32]) + if not animation: + list = [fn for fn in os.listdir("./wqflask/static/gif/error") if fn.endswith(".gif") ] + animation = random.choice(list) + + resp = make_response(render_template("error.html",message=err_msg,stack=formatted_lines,error_image=animation)) + + # logger.error("Set cookie %s with %s" % (err_msg, animation)) + resp.set_cookie(err_msg[:32],animation) + return resp + @app.route("/") def index_page(): logger.info("Sending index_page") @@ -407,6 +439,7 @@ def mapping_results_container_page(): @app.route("/marker_regression", methods=('POST',)) def marker_regression_page(): initial_start_vars = request.form + logger.debug("Marker regression called with initial_start_vars:", initial_start_vars.items()) temp_uuid = initial_start_vars['temp_uuid'] wanted = ( 'trait_id', @@ -444,11 +477,11 @@ def marker_regression_page(): 'mapmethod_rqtl_geno', 'mapmodel_rqtl_geno' ) - logger.info("Marker regression called with initial_start_vars:", initial_start_vars) start_vars = {} for key, value in initial_start_vars.iteritems(): if key in wanted or key.startswith(('value:')): start_vars[key] = value + logger.debug("Marker regression called with start_vars:", start_vars) version = "v3" key = "marker_regression:{}:".format(version) + json.dumps(start_vars, sort_keys=True) @@ -577,7 +610,7 @@ def network_graph_page(): return render_template("network_graph.html", **template_vars.__dict__) else: return render_template("empty_collection.html", **{'tool':'Network Graph'}) - + @app.route("/corr_compute", methods=('POST',)) def corr_compute_page(): logger.info("In corr_compute, request.form is:", pf(request.form)) |
