gatk-3.8/python/CoverageEval.py

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#!/usr/bin/env python
import sys, itertools, FlatFileTable
from enum import Enum
def subset_list_by_indices(indices, list):
subset = []
for index in indices:
subset.append(list[index])
return subset
def chunk_generator(record_gen, key_fields):
"""Input:
record_gen: generator that produces dictionaries (records in database speak)
key_fields: keys in each dictionary used to determine chunk membership
Output:
locus_chunk: list of consecutive lines that have the same key_fields"""
locus_chunk = []
last_key = ""
first_record = True
for record in record_gen:
key = [record[f] for f in key_fields]
if key == last_key or first_record:
locus_chunk.append(record)
first_record = False
else:
if locus_chunk != []:
yield locus_chunk
locus_chunk = [record]
last_key = key
yield locus_chunk
class call_stats:
def __init__(self, call_type, coverage): #, acc_conf_calls, conf_call_rate, cum_corr_calls, cum_calls, coverage):
self.call_type = call_type
self.coverage = coverage
self.calls = 0
self.conf_ref_calls = 0
self.conf_het_calls = 0
self.conf_hom_calls = 0
self.conf_var_calls = 0
self.conf_genotype_calls = 0
self.conf_refvar_calls = 0
self.correct_genotype = 0
self.correct_refvar = 0
def add_stat(self, calls, conf_ref_calls, conf_het_calls, conf_hom_calls, conf_var_calls, conf_genotype_calls, conf_refvar_calls, correct_genotype, correct_refvar):
self.calls += calls
self.conf_ref_calls += conf_ref_calls
self.conf_het_calls += conf_het_calls
self.conf_hom_calls += conf_hom_calls
self.conf_var_calls += conf_var_calls
self.conf_genotype_calls += conf_genotype_calls
self.conf_refvar_calls += conf_refvar_calls
self.correct_genotype += correct_genotype
self.correct_refvar += correct_refvar
@staticmethod
def calc_discovery_stats(chunk):
conf_calls = 0
correct_genotype = 0
calls = 0
for record in chunk:
calls += 1
if abs(float(record["BtrLod"])) >= 5:
conf_calls += 1
if call_type.discovery_call_correct(record):
correct_genotype += 1
return correct_genotype, conf_calls, calls
@staticmethod
def calc_genotyping_stats(chunk):
conf_calls = 0
correct_genotype = 0
calls = 0
for record in chunk:
calls += 1
if abs(float(record["BtnbLod"])) >= 5:
conf_calls += 1
if call_type.genotyping_call_correct(record):
correct_genotype += 1
return correct_genotype, conf_calls, calls
@staticmethod
def stats_header():
return "TrueGenotype,Coverage,AccuracyConfidentGenotypingCalls,ConfidentGenotypingCallRate,AccuracyConfidentDiscoveryCalls,ConfidentDiscoveryCallRate,Calls,ConfRefCalls,ConfHetCalls,ConfHomCalls,ConfGenotypeCalls,CorrectGenotypes,ConfVarCalls,ConfDiscoveryCalls,CorrectDiscovery"
def __str__(self):
return ",".join(map(str, (self.calls, self.conf_ref_calls, self.conf_het_calls, self.conf_hom_calls, self.conf_genotype_calls, self.correct_genotype, self.conf_var_calls, self.conf_refvar_calls, self.correct_refvar)))
def stats_str(self):
return "%s,%d,%.5f,%.5f,%.5f,%.5f,%s" % (self.call_type, self.coverage, float(self.correct_genotype) / max(self.conf_genotype_calls,1), float(self.conf_genotype_calls) / max(self.calls,1), float(self.correct_refvar) / max(self.conf_refvar_calls,1), float(self.conf_refvar_calls) / max(self.calls,1), self.__str__())
class call_type:
"""Class that returns an Enum with the type of call provided by a record"""
call_types_3_state = Enum("HomozygousSNP","HeterozygousSNP","HomozygousReference")
call_types_3_state_short = Enum("Hom","Het","Ref")
call_types_2_state = Enum("Variant","Reference")
@staticmethod
def from_record_3_state(ref, genotype): # record):
"""Given reference base as string, determine whether called genotype is homref, het, homvar"""
#ref = record["ReferenceBase"][0]
#genotype = record["HapmapChipGenotype"]
return call_type.call_types_3_state[genotype.count(ref)]
@staticmethod
def from_record_2_state(ref, genotype):
"""Given reference base as string, determine whether called genotype is ref or var"""
#ref = record["ReferenceBase"][0]
#genotype = record["HapmapChipGenotype"]
return call_type.call_types_2_state[0] if genotype.count(ref) < 2 else call_type.call_types_2_state[1]
@staticmethod
def genotyping_call_correct(record):
return record["HapmapChipGenotype"] == record["BestGenotype"]
@staticmethod
def discovery_call_correct(record):
return call_type.from_record_2_state(record["ReferenceBase"][0], record["HapmapChipGenotype"]) == call_type.from_record_2_state(record["ReferenceBase"][0], record["BestGenotype"])
def print_record_debug(rec):
print "TEST Genotyping:", call_type.genotyping_call_correct(rec)
print "TEST Discovery:", call_type.discovery_call_correct(rec)
print "DIFF:", call_type.genotyping_call_correct(rec) != call_type.discovery_call_correct(rec)
print "\n".join([" %20s => '%s'" % (k,v) for k,v in sorted(rec.items())])
print call_type.from_record_2_state(rec["ReferenceBase"][0],rec["HapmapChipGenotype"])
print call_type.from_record_2_state(rec["ReferenceBase"][0],rec["BestGenotype"])
print
def aggregate_stats(filename, max_loci, table_filename, debug):
aggregate = dict()
fout = open(table_filename,"w")
fout.write(call_stats.stats_header()+"\n")
locus_gen = chunk_generator(FlatFileTable.record_generator(filename, None), ("Sequence","Position"))
for index, locus_chunk in enumerate(locus_gen):
if index >= max_loci:
break
if (index % 1000) == 0:
sys.stderr.write( str(index)+" loci processed, at: "+locus_chunk[0]["Sequence"]+":"+locus_chunk[0]["Position"]+"\n")
covs = dict()
coverage_chunk_gen = chunk_generator(locus_chunk, ("DownsampledCoverage", "Sequence", "Position"))
for cov_chunk in coverage_chunk_gen:
first_record = cov_chunk[0]
#stat = call_stats.calc_stats(cov_chunk)
for record in cov_chunk:
hapmap_genotyping_call_type = call_type.from_record_3_state(record["ReferenceBase"][0],record["HapmapChipGenotype"])
key = hapmap_genotyping_call_type, int(record["DownsampledCoverage"])
#key = call_type.from_record_3_state(record)#, int(record["DownsampledCoverage"])
record["DownsampledCoverage"] = int(record["DownsampledCoverage"])
record["HapmapChipCallType"] = hapmap_genotyping_call_type
value = record
correct_genotype, conf_genotype_calls, genotype_calls = call_stats.calc_genotyping_stats([record])
correct_refvar, conf_refvar_calls, refvar_calls = call_stats.calc_discovery_stats([record])
assert(genotype_calls == refvar_calls)
conf_ref_calls = 0
conf_het_calls = 0
conf_hom_calls = 0
best_genotyping_call_type = call_type.from_record_3_state(record["ReferenceBase"][0],record["BestGenotype"])
if conf_genotype_calls:
if best_genotyping_call_type.index == 0: conf_hom_calls = 1
if best_genotyping_call_type.index == 1: conf_het_calls = 1
if best_genotyping_call_type.index == 2: conf_ref_calls = 1
conf_var_calls = 0
if conf_refvar_calls:
this_variant_call_type = call_type.from_record_2_state(record["ReferenceBase"][0],record["BestGenotype"])
conf_var_calls = 1 if this_variant_call_type.index == 0 else 0
aggregate.setdefault(key, call_stats(*key))
#print ",".join(map(str,(genotype_calls, conf_ref_calls, conf_het_calls, conf_hom_calls, conf_var_calls, conf_genotype_calls, conf_refvar_calls, correct_genotype, correct_refvar)))
aggregate[key].add_stat(genotype_calls, conf_ref_calls, conf_het_calls, conf_hom_calls, conf_var_calls, conf_genotype_calls, conf_refvar_calls, correct_genotype, correct_refvar)
if debug:# and conf_refvar_calls:
print "KEYS:",key
print_record_debug(record)
for key, records in sorted(aggregate.items()):
fout.write(records.stats_str()+"\n")
fout.close()
#return aggregate
class weighted_avg:
def __init__(self):
self.sum = 0.0
self.count = 0
def add(self, value, counts):
self.sum += value*counts
self.count += counts
def return_avg(self):
return float(self.sum) / max(self.count,1)
def stats_from_hist(depth_hist_filename, stats_filename, variant_eval_dir, depth_multiplier=1.0):
#hist_zero = {"CallType" : ,"Coverage","AccuracyConfidentCalls","ConfidentCallRate","CumCorrectCalls","CumCalls","CumgCorrectFraction"}
#prob_genotype = [1e-5, 1e-3, 1-1e-3]
#prob_genotype = [0.37, 0.62, .0]
#prob_genotype = [0.203, 0.304, .491]
#prob_genotype = [0.216, 0.302, .481]
#prob_genotype = [0.205, 0.306, 0.491] # Based on CEU NA12878 actual hapmap chip calls
prob_genotype = [0.213, 0.313, 0.474] # Based on YRB NA19240 actual hapmap chip calls
hist = []
hist_gen = FlatFileTable.record_generator(depth_hist_filename, sep=" ", skip_n_lines=3)
for index, record in enumerate(hist_gen):
assert int(record["depth"]) == index
hist.append(int(record["count"]))
stats_dict = dict()
stats_gen = FlatFileTable.record_generator(stats_filename, sep=",")
for record in stats_gen:
key1 = int(record["Coverage"])
key2 = record["TrueGenotype"]
#print key2
stats_dict.setdefault(key1, dict()) # create a nested dict if it doesn't exist
stats_dict[key1][key2] = record # create an entry for these keys
acc = dict()
call_rate = dict()
conf_calls = dict()
start = 1
end = 1000
for depth, depth_count in enumerate(hist[start:end+1],start): # For Cd = depth count
#print "DEPTH: "+str(depth)
try:
depth = max(int(float(depth*depth_multiplier)),1)
depth_entries = stats_dict[depth]
except KeyError:
print "Stopped on depth",depth
break
if True:
for true_genotype, stat in depth_entries.items(): # For t (SNP type) = true_genotype
#print "TRUE_GENOTYPE: "+str(true_genotype)
for genotype in call_type.call_types_3_state:
conf_calls.setdefault(genotype, 0.0)
prob_conf_x_call = float(stat["Conf"+str(call_type.call_types_3_state_short[genotype.index])+"Calls"])/float(stat["Calls"])
conf_calls[genotype] += depth_count * prob_conf_x_call * prob_genotype[genotype.index]
#if genotype.index == 1:
# print "%.5f " % prob_conf_x_call, depth, depth_count, conf_calls[genotype], int(stat["Conf"+str(call_type.call_types_3_state_short[genotype.index])+"Calls"]), int(stat["Calls"])
acc.setdefault(true_genotype,weighted_avg())
call_rate.setdefault(true_genotype,weighted_avg())
acc[true_genotype].add(float(stat["AccuracyConfidentGenotypingCalls"]), depth_count)
call_rate[true_genotype].add(float(stat["ConfidentGenotypingCallRate"]), depth_count)
import numpy
for genotype in call_type.call_types_3_state:
print "%19s accuracy : %.3f" % (str(genotype), acc[str(genotype)].return_avg())
print "%19s call rate: %.3f" % (str(genotype), call_rate[str(genotype)].return_avg())
print "\nExpected performance given perfect accuracy and call rate:"
print "%19s %7s %7s %7s" % ("", "Actual", "Perfect", "Diff.")
total_hist_sites = numpy.sum(hist)
for genotype in call_type.call_types_3_state:
predicted = conf_calls[genotype]
perfect = prob_genotype[genotype.index]*total_hist_sites
diff = perfect - predicted
print "%19s calls: %7d %7d %7d" % (genotype, predicted, perfect, diff)
#stats_gen = FlatFileTable.record_generator(stats_filename, sep=",")
#for chunk in chunk_generator(stats_gen, key_fields=("True_Genotype")):
print "\nCoverage histogram mean: %.2f" % numpy.average(range(len(hist)), weights=hist)
# STEM AND LEAF PLOT
# If VariantEval directory given, compare with those results
def usage(parser):
parser.print_usage()
sys.exit()
if __name__ == "__main__":
from optparse import OptionParser
parser = OptionParser()
parser.add_option("-c", "--genotype_call_file", help="GELI file to use in generating coverage stat table", dest="genotype_filename", )
parser.add_option("-s", "--stats_file", help="file to containing empirical genotyping stats", dest="stats_filename", default=None)
parser.add_option("-g", "--histogram_file", help="file containing counts of each depth of coverage", dest="hist_filename")
parser.add_option("-m", "--max_loci", help="maximum number of loci to parse (for debugging)", default=sys.maxint, dest="max_loci", type="int")
parser.add_option("-e", "--evaluate", help="evaluate genotypes; requires a stats file and a histogram file", default=False, dest="evaluate_genotypes", action="store_true")
parser.add_option("-d", "--debug", help="provide debugging output", default=False, dest="debug", action="store_true")
parser.add_option("-p", "--depth_multiplier", help="multiply all depths in histogram by this value; for \"downsampling\" depth", default=1.0, dest="depth_multiplier", type=float)
parser.add_option("-v", "--variant_eval_dir", help="directory with output of VariantEval to compare this prediction to", default=None, dest="variant_eval_dir")
(options, args) = parser.parse_args()
if not options.evaluate_genotypes:
print "Creating performance tables from genotypes file"
#if options.stats_filename == None:
# sys.exit("Must provide -s stats fliname option")
if options.genotype_filename == None:
sys.exit("Must provide -c genotype call filename option")
stats_filename = options.stats_filename if options.stats_filename != None else options.genotype_filename+".stats"
aggregate_stats(options.genotype_filename, options.max_loci, options.stats_filename, options.debug)
else:
print "Evaluating genotypes"
print "Depth multiplier:",options.depth_multiplier
if options.hist_filename == None:
sys.exit("Must provide -g histogram filename option")
if options.stats_filename == None:
sys.exit("Must provide -s stats fliname option")
stats_from_hist(options.hist_filename, options.stats_filename, options.variant_eval_dir, options.depth_multiplier)