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authorzsloan2021-11-11 11:23:39 -0600
committerGitHub2021-11-11 11:23:39 -0600
commit8c77af63efae6f06d7c7c3269fc0e41811a8037a (patch)
tree9ffa4b84fd36f09e772db3e218bc980999324c41 /gn3/computations
parent607c6e627c23c1bce3b199b145855182ab51b211 (diff)
parent249b85102063debfeeb1b0565956059b8a3af1cf (diff)
downloadgenenetwork3-8c77af63efae6f06d7c7c3269fc0e41811a8037a.tar.gz
Merge branch 'main' into feature/add_rqtl_pairscan
Diffstat (limited to 'gn3/computations')
-rw-r--r--gn3/computations/biweight.py27
-rw-r--r--gn3/computations/correlations.py41
-rw-r--r--gn3/computations/partial_correlations.py289
-rw-r--r--gn3/computations/wgcna.py49
4 files changed, 354 insertions, 52 deletions
diff --git a/gn3/computations/biweight.py b/gn3/computations/biweight.py
deleted file mode 100644
index 7accd0c..0000000
--- a/gn3/computations/biweight.py
+++ /dev/null
@@ -1,27 +0,0 @@
-"""module contains script to call biweight midcorrelation in R"""
-import subprocess
-
-from typing import List
-from typing import Tuple
-
-from gn3.settings import BIWEIGHT_RSCRIPT
-
-
-def calculate_biweight_corr(trait_vals: List,
- target_vals: List,
- path_to_script: str = BIWEIGHT_RSCRIPT,
- command: str = "Rscript"
- ) -> Tuple[float, float]:
- """biweight function"""
-
- args_1 = ' '.join(str(trait_val) for trait_val in trait_vals)
- args_2 = ' '.join(str(target_val) for target_val in target_vals)
- cmd = [command, path_to_script] + [args_1] + [args_2]
-
- results = subprocess.check_output(cmd, universal_newlines=True)
- try:
- (corr_coeff, p_val) = tuple(
- [float(y.strip()) for y in results.split()])
- return (corr_coeff, p_val)
- except Exception as error:
- raise error
diff --git a/gn3/computations/correlations.py b/gn3/computations/correlations.py
index bb13ff1..c5c56db 100644
--- a/gn3/computations/correlations.py
+++ b/gn3/computations/correlations.py
@@ -1,6 +1,7 @@
"""module contains code for correlations"""
import math
import multiprocessing
+from contextlib import closing
from typing import List
from typing import Tuple
@@ -8,7 +9,7 @@ from typing import Optional
from typing import Callable
import scipy.stats
-from gn3.computations.biweight import calculate_biweight_corr
+import pingouin as pg
def map_shared_keys_to_values(target_sample_keys: List,
@@ -49,13 +50,9 @@ def normalize_values(a_values: List,
([2.3, 4.1, 5], [3.4, 6.2, 4.1], 3)
"""
- a_new = []
- b_new = []
for a_val, b_val in zip(a_values, b_values):
if (a_val and b_val is not None):
- a_new.append(a_val)
- b_new.append(b_val)
- return a_new, b_new, len(a_new)
+ yield a_val, b_val
def compute_corr_coeff_p_value(primary_values: List, target_values: List,
@@ -81,8 +78,10 @@ def compute_sample_r_correlation(trait_name, corr_method, trait_vals,
correlation coeff and p value
"""
- (sanitized_traits_vals, sanitized_target_vals,
- num_overlap) = normalize_values(trait_vals, target_samples_vals)
+
+ sanitized_traits_vals, sanitized_target_vals = list(
+ zip(*list(normalize_values(trait_vals, target_samples_vals))))
+ num_overlap = len(sanitized_traits_vals)
if num_overlap > 5:
@@ -102,11 +101,10 @@ package :not packaged in guix
"""
- try:
- results = calculate_biweight_corr(x_val, y_val)
- return results
- except Exception as error:
- raise error
+ results = pg.corr(x_val, y_val, method="bicor")
+ corr_coeff = results["r"].values[0]
+ p_val = results["p-val"].values[0]
+ return (corr_coeff, p_val)
def filter_shared_sample_keys(this_samplelist,
@@ -115,13 +113,9 @@ def filter_shared_sample_keys(this_samplelist,
filter the values using the shared keys
"""
- this_vals = []
- target_vals = []
for key, value in target_samplelist.items():
if key in this_samplelist:
- target_vals.append(value)
- this_vals.append(this_samplelist[key])
- return (this_vals, target_vals)
+ yield this_samplelist[key], value
def fast_compute_all_sample_correlation(this_trait,
@@ -140,9 +134,10 @@ def fast_compute_all_sample_correlation(this_trait,
for target_trait in target_dataset:
trait_name = target_trait.get("trait_id")
target_trait_data = target_trait["trait_sample_data"]
- processed_values.append((trait_name, corr_method, *filter_shared_sample_keys(
- this_trait_samples, target_trait_data)))
- with multiprocessing.Pool(4) as pool:
+ processed_values.append((trait_name, corr_method,
+ list(zip(*list(filter_shared_sample_keys(
+ this_trait_samples, target_trait_data))))))
+ with closing(multiprocessing.Pool()) as pool:
results = pool.starmap(compute_sample_r_correlation, processed_values)
for sample_correlation in results:
@@ -173,8 +168,8 @@ def compute_all_sample_correlation(this_trait,
for target_trait in target_dataset:
trait_name = target_trait.get("trait_id")
target_trait_data = target_trait["trait_sample_data"]
- this_vals, target_vals = filter_shared_sample_keys(
- this_trait_samples, target_trait_data)
+ this_vals, target_vals = list(zip(*list(filter_shared_sample_keys(
+ this_trait_samples, target_trait_data))))
sample_correlation = compute_sample_r_correlation(
trait_name=trait_name,
diff --git a/gn3/computations/partial_correlations.py b/gn3/computations/partial_correlations.py
new file mode 100644
index 0000000..07dc16d
--- /dev/null
+++ b/gn3/computations/partial_correlations.py
@@ -0,0 +1,289 @@
+"""
+This module deals with partial correlations.
+
+It is an attempt to migrate over the partial correlations feature from
+GeneNetwork1.
+"""
+
+from functools import reduce
+from typing import Any, Tuple, Sequence
+from scipy.stats import pearsonr, spearmanr
+
+from gn3.settings import TEXTDIR
+from gn3.data_helpers import parse_csv_line
+
+def control_samples(controls: Sequence[dict], sampleslist: Sequence[str]):
+ """
+ Fetches data for the control traits.
+
+ This migrates `web/webqtl/correlation/correlationFunction.controlStrain` in
+ GN1, with a few modifications to the arguments passed in.
+
+ PARAMETERS:
+ controls: A map of sample names to trait data. Equivalent to the `cvals`
+ value in the corresponding source function in GN1.
+ sampleslist: A list of samples. Equivalent to `strainlst` in the
+ corresponding source function in GN1
+ """
+ def __process_control__(trait_data):
+ def __process_sample__(acc, sample):
+ if sample in trait_data["data"].keys():
+ sample_item = trait_data["data"][sample]
+ val = sample_item["value"]
+ if val is not None:
+ return (
+ acc[0] + (sample,),
+ acc[1] + (val,),
+ acc[2] + (sample_item["variance"],))
+ return acc
+ return reduce(
+ __process_sample__, sampleslist, (tuple(), tuple(), tuple()))
+
+ return reduce(
+ lambda acc, item: (
+ acc[0] + (item[0],),
+ acc[1] + (item[1],),
+ acc[2] + (item[2],),
+ acc[3] + (len(item[0]),),
+ ),
+ [__process_control__(trait_data) for trait_data in controls],
+ (tuple(), tuple(), tuple(), tuple()))
+
+def dictify_by_samples(samples_vals_vars: Sequence[Sequence]) -> Sequence[dict]:
+ """
+ Build a sequence of dictionaries from a sequence of separate sequences of
+ samples, values and variances.
+
+ This is a partial migration of
+ `web.webqtl.correlation.correlationFunction.fixStrains` function in GN1.
+ This implementation extracts code that will find common use, and that will
+ find use in more than one place.
+ """
+ return tuple(
+ {
+ sample: {"sample_name": sample, "value": val, "variance": var}
+ for sample, val, var in zip(*trait_line)
+ } for trait_line in zip(*(samples_vals_vars[0:3])))
+
+def fix_samples(primary_trait: dict, control_traits: Sequence[dict]) -> Sequence[Sequence[Any]]:
+ """
+ Corrects sample_names, values and variance such that they all contain only
+ those samples that are common to the reference trait and all control traits.
+
+ This is a partial migration of the
+ `web.webqtl.correlation.correlationFunction.fixStrain` function in GN1.
+ """
+ primary_samples = tuple(
+ present[0] for present in
+ ((sample, all(sample in control.keys() for control in control_traits))
+ for sample in primary_trait.keys())
+ if present[1])
+ control_vals_vars: tuple = reduce(
+ lambda acc, x: (acc[0] + (x[0],), acc[1] + (x[1],)),
+ ((item["value"], item["variance"])
+ for sublist in [tuple(control.values()) for control in control_traits]
+ for item in sublist),
+ (tuple(), tuple()))
+ return (
+ primary_samples,
+ tuple(primary_trait[sample]["value"] for sample in primary_samples),
+ control_vals_vars[0],
+ tuple(primary_trait[sample]["variance"] for sample in primary_samples),
+ control_vals_vars[1])
+
+def find_identical_traits(
+ primary_name: str, primary_value: float, control_names: Tuple[str, ...],
+ control_values: Tuple[float, ...]) -> Tuple[str, ...]:
+ """
+ Find traits that have the same value when the values are considered to
+ 3 decimal places.
+
+ This is a migration of the
+ `web.webqtl.correlation.correlationFunction.findIdenticalTraits` function in
+ GN1.
+ """
+ def __merge_identicals__(
+ acc: Tuple[str, ...],
+ ident: Tuple[str, Tuple[str, ...]]) -> Tuple[str, ...]:
+ return acc + ident[1]
+
+ def __dictify_controls__(acc, control_item):
+ ckey = "{:.3f}".format(control_item[0])
+ return {**acc, ckey: acc.get(ckey, tuple()) + (control_item[1],)}
+
+ return (reduce(## for identical control traits
+ __merge_identicals__,
+ (item for item in reduce(# type: ignore[var-annotated]
+ __dictify_controls__, zip(control_values, control_names),
+ {}).items() if len(item[1]) > 1),
+ tuple())
+ or
+ reduce(## If no identical control traits, try primary and controls
+ __merge_identicals__,
+ (item for item in reduce(# type: ignore[var-annotated]
+ __dictify_controls__,
+ zip((primary_value,) + control_values,
+ (primary_name,) + control_names), {}).items()
+ if len(item[1]) > 1),
+ tuple()))
+
+def tissue_correlation(
+ primary_trait_values: Tuple[float, ...],
+ target_trait_values: Tuple[float, ...],
+ method: str) -> Tuple[float, float]:
+ """
+ Compute the correlation between the primary trait values, and the values of
+ a single target value.
+
+ This migrates the `cal_tissue_corr` function embedded in the larger
+ `web.webqtl.correlation.correlationFunction.batchCalTissueCorr` function in
+ GeneNetwork1.
+ """
+ def spearman_corr(*args):
+ result = spearmanr(*args)
+ return (result.correlation, result.pvalue)
+
+ method_fns = {"pearson": pearsonr, "spearman": spearman_corr}
+
+ assert len(primary_trait_values) == len(target_trait_values), (
+ "The lengths of the `primary_trait_values` and `target_trait_values` "
+ "must be equal")
+ assert method in method_fns.keys(), (
+ "Method must be one of: {}".format(",".join(method_fns.keys())))
+
+ corr, pvalue = method_fns[method](primary_trait_values, target_trait_values)
+ return (round(corr, 10), round(pvalue, 10))
+
+def batch_computed_tissue_correlation(
+ primary_trait_values: Tuple[float, ...], target_traits_dict: dict,
+ method: str) -> Tuple[dict, dict]:
+ """
+ This is a migration of the
+ `web.webqtl.correlation.correlationFunction.batchCalTissueCorr` function in
+ GeneNetwork1
+ """
+ def __corr__(acc, target):
+ corr = tissue_correlation(primary_trait_values, target[1], method)
+ return ({**acc[0], target[0]: corr[0]}, {**acc[0], target[1]: corr[1]})
+ return reduce(__corr__, target_traits_dict.items(), ({}, {}))
+
+def correlations_of_all_tissue_traits(
+ primary_trait_symbol_value_dict: dict, symbol_value_dict: dict,
+ method: str) -> Tuple[dict, dict]:
+ """
+ Computes and returns the correlation of all tissue traits.
+
+ This is a migration of the
+ `web.webqtl.correlation.correlationFunction.calculateCorrOfAllTissueTrait`
+ function in GeneNetwork1.
+ """
+ primary_trait_values = tuple(primary_trait_symbol_value_dict.values())[0]
+ return batch_computed_tissue_correlation(
+ primary_trait_values, symbol_value_dict, method)
+
+def good_dataset_samples_indexes(
+ samples: Tuple[str, ...],
+ samples_from_file: Tuple[str, ...]) -> Tuple[int, ...]:
+ """
+ Return the indexes of the items in `samples_from_files` that are also found
+ in `samples`.
+
+ This is a partial migration of the
+ `web.webqtl.correlation.PartialCorrDBPage.getPartialCorrelationsFast`
+ function in GeneNetwork1.
+ """
+ return tuple(sorted(
+ samples_from_file.index(good) for good in
+ set(samples).intersection(set(samples_from_file))))
+
+def determine_partials(
+ primary_vals, control_vals, all_target_trait_names,
+ all_target_trait_values, method):
+ """
+ This **WILL** be a migration of
+ `web.webqtl.correlation.correlationFunction.determinePartialsByR` function
+ in GeneNetwork1.
+
+ The function in GeneNetwork1 contains code written in R that is then used to
+ compute the partial correlations.
+ """
+ ## This function is not implemented at this stage
+ return tuple(
+ primary_vals, control_vals, all_target_trait_names,
+ all_target_trait_values, method)
+
+def compute_partial_correlations_fast(# pylint: disable=[R0913, R0914]
+ samples, primary_vals, control_vals, database_filename,
+ fetched_correlations, method: str, correlation_type: str) -> Tuple[
+ float, Tuple[float, ...]]:
+ """
+ This is a partial migration of the
+ `web.webqtl.correlation.PartialCorrDBPage.getPartialCorrelationsFast`
+ function in GeneNetwork1.
+ """
+ assert method in ("spearman", "pearson")
+ with open(f"{TEXTDIR}/{database_filename}", "r") as dataset_file:
+ dataset = tuple(dataset_file.readlines())
+
+ good_dataset_samples = good_dataset_samples_indexes(
+ samples, parse_csv_line(dataset[0])[1:])
+
+ def __process_trait_names_and_values__(acc, line):
+ trait_line = parse_csv_line(line)
+ trait_name = trait_line[0]
+ trait_data = trait_line[1:]
+ if trait_name in fetched_correlations.keys():
+ return (
+ acc[0] + (trait_name,),
+ acc[1] + tuple(
+ trait_data[i] if i in good_dataset_samples else None
+ for i in range(len(trait_data))))
+ return acc
+
+ processed_trait_names_values: tuple = reduce(
+ __process_trait_names_and_values__, dataset[1:], (tuple(), tuple()))
+ all_target_trait_names: Tuple[str, ...] = processed_trait_names_values[0]
+ all_target_trait_values: Tuple[float, ...] = processed_trait_names_values[1]
+
+ all_correlations = determine_partials(
+ primary_vals, control_vals, all_target_trait_names,
+ all_target_trait_values, method)
+ ## Line 772 to 779 in GN1 are the cause of the weird complexity in the
+ ## return below. Once the surrounding code is successfully migrated and
+ ## reworked, this complexity might go away, by getting rid of the
+ ## `correlation_type` parameter
+ return len(all_correlations), tuple(
+ corr + (
+ (fetched_correlations[corr[0]],) if correlation_type == "literature"
+ else fetched_correlations[corr[0]][0:2])
+ for idx, corr in enumerate(all_correlations))
+
+def partial_correlation_matrix(
+ xdata: Tuple[float, ...], ydata: Tuple[float, ...],
+ zdata: Tuple[float, ...], method: str = "pearsons",
+ omit_nones: bool = True) -> float:
+ """
+ Computes the partial correlation coefficient using the
+ 'variance-covariance matrix' method
+
+ This is a partial migration of the
+ `web.webqtl.correlation.correlationFunction.determinPartialsByR` function in
+ GeneNetwork1, specifically the `pcor.mat` function written in the R
+ programming language.
+ """
+ return 0
+
+def partial_correlation_recursive(
+ xdata: Tuple[float, ...], ydata: Tuple[float, ...],
+ zdata: Tuple[float, ...], method: str = "pearsons",
+ omit_nones: bool = True) -> float:
+ """
+ Computes the partial correlation coefficient using the 'recursive formula'
+ method
+
+ This is a partial migration of the
+ `web.webqtl.correlation.correlationFunction.determinPartialsByR` function in
+ GeneNetwork1, specifically the `pcor.rec` function written in the R
+ programming language.
+ """
+ return 0
diff --git a/gn3/computations/wgcna.py b/gn3/computations/wgcna.py
index fd508fa..ab12fe7 100644
--- a/gn3/computations/wgcna.py
+++ b/gn3/computations/wgcna.py
@@ -3,8 +3,11 @@
import os
import json
import uuid
-from gn3.settings import TMPDIR
+import subprocess
+import base64
+
+from gn3.settings import TMPDIR
from gn3.commands import run_cmd
@@ -14,12 +17,46 @@ def dump_wgcna_data(request_data: dict):
temp_file_path = os.path.join(TMPDIR, filename)
+ request_data["TMPDIR"] = TMPDIR
+
with open(temp_file_path, "w") as output_file:
json.dump(request_data, output_file)
return temp_file_path
+def stream_cmd_output(socketio, request_data, cmd: str):
+ """function to stream in realtime"""
+ # xtodo syncing and closing /edge cases
+
+ socketio.emit("output", {"data": f"calling you script {cmd}"},
+ namespace="/", room=request_data["socket_id"])
+ results = subprocess.Popen(
+ cmd, stdout=subprocess.PIPE, stderr=subprocess.STDOUT, shell=True)
+
+ if results.stdout is not None:
+
+ for line in iter(results.stdout.readline, b""):
+ socketio.emit("output",
+ {"data": line.decode("utf-8").rstrip()},
+ namespace="/", room=request_data["socket_id"])
+
+ socketio.emit(
+ "output", {"data":
+ "parsing the output results"}, namespace="/",
+ room=request_data["socket_id"])
+
+
+def process_image(image_loc: str) -> bytes:
+ """encode the image"""
+
+ try:
+ with open(image_loc, "rb") as image_file:
+ return base64.b64encode(image_file.read())
+ except FileNotFoundError:
+ return b""
+
+
def compose_wgcna_cmd(rscript_path: str, temp_file_path: str):
"""function to componse wgcna cmd"""
# (todo):issue relative paths to abs paths
@@ -32,6 +69,8 @@ def call_wgcna_script(rscript_path: str, request_data: dict):
generated_file = dump_wgcna_data(request_data)
cmd = compose_wgcna_cmd(rscript_path, generated_file)
+ # stream_cmd_output(request_data, cmd) disable streaming of data
+
try:
run_cmd_results = run_cmd(cmd)
@@ -40,8 +79,14 @@ def call_wgcna_script(rscript_path: str, request_data: dict):
if run_cmd_results["code"] != 0:
return run_cmd_results
+
+ output_file_data = json.load(outputfile)
+ output_file_data["output"]["image_data"] = process_image(
+ output_file_data["output"]["imageLoc"]).decode("ascii")
+ # json format only supports unicode string// to get image data reconvert
+
return {
- "data": json.load(outputfile),
+ "data": output_file_data,
**run_cmd_results
}
except FileNotFoundError: