Mercurial > repos > iuc > medaka_consensus
diff annotateVCF.py @ 4:84dcccebad3d draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/medaka commit e80b649094384fc6d7a8f917300db3550cc99a44"
author | iuc |
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date | Tue, 01 Sep 2020 03:07:44 -0400 |
parents | |
children | 22f6a0e7424f |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/annotateVCF.py Tue Sep 01 03:07:44 2020 -0400 @@ -0,0 +1,398 @@ +#!/usr/bin/env python3 + +# Takes in VCF file and a samtools mpileup output file +# Fills in annotation for the VCF file including AF, DP +# SB, and DP4 +# +# Usage statement: +# python annotateVCF.py in_vcf.vcf in_mpileup.txt out_vcf.vcf +# +# Can generate in_mileup.txt with samtools mpileup (and can restrict which sites to generate pileups for with in_vcf.vcf) + +# 08/24/2020 - Nathan P. Roach, natproach@gmail.com + +import sys +from math import isnan, log10 + +from scipy.stats import fisher_exact + + +def pval_to_phredqual(pval): + return int(round(-10. * log10(pval))) + + +def parseSimpleSNPpileup(fields, ref_base, alt_base): + base_to_idx = { + 'A': 0, + 'a': 0, + 'T': 1, + 't': 1, + 'C': 2, + 'c': 2, + 'G': 3, + 'g': 3 + } + + base_to_idx_stranded = { + 'A': 0, + 'T': 1, + 'C': 2, + 'G': 3, + 'a': 4, + 't': 5, + 'c': 6, + 'g': 7 + } + ref_base2 = fields[2] + counts = [0, 0, 0, 0] + stranded_counts = [0, 0, 0, 0, 0, 0, 0, 0] + ref_idx = base_to_idx[fields[2]] + dp = int(fields[3]) + carrot_flag = False + ins_flag = False + ins_str = "" + ins_len = 0 + insertion = "" + del_flag = False + del_str = "" + del_len = 0 + deletion = "" + # dollar_flag = False + for base in fields[4]: + if carrot_flag: + carrot_flag = False + continue + if ins_len > 0: + insertion += base + ins_len -= 1 + continue + if del_len > 0: + deletion += base + del_len -= 1 + continue + if ins_flag: + if base.isdigit(): + ins_str += base + else: + ins_len = int(ins_str) - 1 + insertion = base + ins_flag = False + elif del_flag: + if base.isdigit(): + del_str += base + else: + del_len = int(del_str) - 1 + deletion = base + del_flag = False + else: + if base == '^': + carrot_flag = True + continue + elif base == '$': + continue + elif base == '+': + ins_flag = True + elif base == '-': + del_flag = True + elif base == '.': + counts[ref_idx] += 1 + stranded_counts[base_to_idx_stranded[ref_base2]] += 1 + elif base == ',': + counts[ref_idx] += 1 + stranded_counts[base_to_idx_stranded[ref_base2.lower()]] += 1 + elif base == 'N' or base == 'n': + continue + elif base == '*': + continue + else: + counts[base_to_idx[base]] += 1 + stranded_counts[base_to_idx_stranded[base]] += 1 + af = float(counts[base_to_idx[alt_base]]) / float(sum(counts)) + if float(sum(stranded_counts[0:4])) == 0: + faf = float("nan") + else: + faf = float(stranded_counts[base_to_idx_stranded[alt_base]]) / float(sum(stranded_counts[0:4])) + if float(sum(stranded_counts[4:])) == 0: + raf = float("nan") + else: + raf = float(stranded_counts[base_to_idx_stranded[alt_base.lower()]]) / float(sum(stranded_counts[4:])) + dp4 = [stranded_counts[base_to_idx_stranded[ref_base]], + stranded_counts[base_to_idx_stranded[ref_base.lower()]], + stranded_counts[base_to_idx_stranded[alt_base]], + stranded_counts[base_to_idx_stranded[alt_base.lower()]]] + return (dp, af, faf, raf, dp4) + + +def parseIndelPileup(fields, ref_base, alt_base): + counts = [0, 0, 0, 0, 0, 0, 0, 0, 0] # indel ref match, indel fwd ref match, indel rev ref match, indel alt match, indel fwd alt match, indel rev alt match, other, other fwd, other rev + ref_base2 = fields[2] + + carrot_flag = False + ins_flag = False + ins_str = "" + ins_len = 0 + del_flag = False + del_str = "" + del_len = 0 + first_iter = True + forward_flag = False + last_seq = "" + last_seq_code = 'b' + for base in fields[4]: + if ins_flag: + if base.isdigit(): + ins_str += base + else: + ins_len = int(ins_str) + ins_flag = False + if del_flag: + if base.isdigit(): + del_str += base + else: + del_len = int(del_str) + del_flag = False + if ins_len > 0: + last_seq += base + last_seq_code = 'i' + ins_len -= 1 + continue + if del_len > 0: + last_seq += base + last_seq_code = 'd' + del_len -= 1 + continue + if carrot_flag: + carrot_flag = False + continue + if base == '.' or base == ','\ + or base == 'A' or base == 'a'\ + or base == 'C' or base == 'c'\ + or base == 'G' or base == 'g'\ + or base == 'T' or base == 't'\ + or base == 'N' or base == 'n'\ + or base == '>' or base == '<'\ + or base == '*' or base == '#': + if first_iter: + first_iter = False + else: + if last_seq_code == 'i': + if last_seq.upper() == alt_base.upper(): + counts[3] += 1 + if forward_flag: + counts[4] += 1 + else: + counts[5] += 1 + else: + counts[6] += 1 + if forward_flag: + counts[7] += 1 + else: + counts[8] += 1 + elif last_seq_code == 'd': + if last_seq.upper() == ref_base.upper(): + counts[3] += 1 + if forward_flag: + counts[4] += 1 + else: + counts[5] += 1 + else: + counts[6] += 1 + if forward_flag: + counts[7] += 1 + else: + counts[8] += 1 + elif last_seq_code == 'b': + if last_seq.upper() == ref_base.upper(): + counts[0] += 1 + if forward_flag: + counts[1] += 1 + else: + counts[2] += 1 + elif last_seq.upper() == alt_base.upper(): + counts[3] += 1 + if forward_flag: + counts[4] += 1 + else: + counts[5] += 1 + else: + counts[6] += 1 + if forward_flag: + counts[7] += 1 + else: + counts[8] += 1 + if base == '.': + last_seq = ref_base2 + forward_flag = True + last_seq_code = 'b' + elif base == ',': + last_seq = ref_base2 + forward_flag = False + last_seq_code = 'b' + elif base == '>' or base == '<' or base == '*' or base == '#': + continue + else: + forward_flag = base.isupper() + last_seq = base.upper() + last_seq_code = 'b' + elif base == '+': + ins_flag = True + ins_str = "" + elif base == '-': + del_flag = True + del_str = "" + elif base == '^': + carrot_flag = True + elif base == '$': + continue + if first_iter: + first_iter = False + + if last_seq_code == 'i': + if last_seq.upper() == alt_base.upper(): + counts[3] += 1 + if forward_flag: + counts[4] += 1 + else: + counts[5] += 1 + else: + counts[6] += 1 + if forward_flag: + counts[7] += 1 + else: + counts[8] += 1 + elif last_seq_code == 'd': + if last_seq.upper() == ref_base.upper(): + counts[3] += 1 + if forward_flag: + counts[4] += 1 + else: + counts[5] += 1 + else: + counts[6] += 1 + if forward_flag: + counts[7] += 1 + else: + counts[8] += 1 + elif last_seq_code == 'b': + if last_seq.upper() == ref_base.upper(): + counts[0] += 1 + if forward_flag: + counts[1] += 1 + else: + counts[2] += 1 + elif last_seq.upper() == alt_base.upper(): + counts[3] += 1 + if forward_flag: + counts[4] += 1 + else: + counts[5] += 1 + else: + counts[6] += 1 + if forward_flag: + counts[7] += 1 + else: + counts[8] += 1 + dp = int(fields[3]) + af = float(counts[3]) / float(sum([counts[0], counts[3], counts[6]])) + if sum([counts[1], counts[4], counts[7]]) == 0: + faf = float("nan") + else: + faf = float(counts[4]) / float(sum([counts[1], counts[4], counts[7]])) + if sum([counts[2], counts[5], counts[8]]) == 0: + raf = float("nan") + else: + raf = float(counts[5]) / float(sum([counts[2], counts[5], counts[8]])) + dp4 = [counts[1], counts[2], counts[4], counts[5]] + return (dp, af, faf, raf, dp4) + + +def annotateVCF(in_vcf_filepath, in_mpileup_filepath, out_vcf_filepath): + in_vcf = open(in_vcf_filepath, 'r') + in_mpileup = open(in_mpileup_filepath, 'r') + out_vcf = open(out_vcf_filepath, 'w') + + # First pass parsing of input vcf, output headerlines + new headerlines, add VCF sites we care about to to_examine (limits memory usage for sites that don't need annotation) + to_examine = {} + for line in in_vcf: + if line[0:2] == "##": + out_vcf.write(line) + elif line[0] == "#": + out_vcf.write("##annotateVCFVersion=0.1\n") + out_vcf.write("##INFO=<ID=DP,Number=1,Type=Integer,Description=\"Raw Depth\">\n") + out_vcf.write("##INFO=<ID=AF,Number=1,Type=Float,Description=\"Allele Frequency\">\n") + out_vcf.write("##INFO=<ID=FAF,Number=1,Type=Float,Description=\"Forward Allele Frequency\">\n") + out_vcf.write("##INFO=<ID=RAF,Number=1,Type=Float,Description=\"Reverse Allele Frequency\">\n") + out_vcf.write("##INFO=<ID=SB,Number=1,Type=Integer,Description=\"Phred-scaled strand bias at this position\">\n") + out_vcf.write("##INFO=<ID=DP4,Number=4,Type=Integer,Description=\"Counts for ref-forward bases, ref-reverse, alt-forward and alt-reverse bases\">\n") + out_vcf.write(line) + else: + fields = line.strip().split() + if fields[0] in to_examine: + to_examine[fields[0]][int(fields[1])] = (fields[3], fields[4]) + else: + to_examine[fields[0]] = {int(fields[1]): (fields[3], fields[4])} + in_vcf.close() + data = {} + + # Populate data dictionary, which relates chromosome and position to the following: + # depth of coverage + # allele frequency + # forward strand allele frequency + # reverse strand allele frequency + # dp4 - depth of coverage of ref allele fwd strand, DOC of ref allele rev strand, DOC of alt allele fwd strand, DOC of alt allele rev strand + for line in in_mpileup: + fields = line.strip().split() + if fields[0] not in to_examine: + continue + if int(fields[1]) not in to_examine[fields[0]]: + continue + (ref_base, alt_base) = to_examine[fields[0]][int(fields[1])] + if len(ref_base.split(',')) > 1: # Can't handle multiple ref alleles + continue + if len(alt_base.split(',')) > 1: # Can't handle multiple alt alleles + continue + if len(ref_base) > 1 or len(alt_base) > 1: + if len(ref_base) > 1 and len(alt_base) > 1: # Can't handle complex indels + continue + data[(fields[0], int(fields[1]))] = parseIndelPileup(fields, ref_base, alt_base) + if len(ref_base) == 1 and len(alt_base) == 1: + data[(fields[0], int(fields[1]))] = parseSimpleSNPpileup(fields, ref_base, alt_base) + in_mpileup.close() + # Reopen vcf, this time, skip header, annotate all the sites for which there is an entry in data dictionary + # (Sites without entries have either multiple ref or alt bases, or have complex indels. Not supported (for now), and not reported as a result) + in_vcf = open(in_vcf_filepath, 'r') + for line in in_vcf: + if line[0] == '#': + continue + fields = line.strip().split('\t') + if (fields[0], int(fields[1])) not in data: + continue + (dp, af, faf, raf, dp4) = data[(fields[0], int(fields[1]))] + dp2x2 = [[dp4[0], dp4[1]], [dp4[2], dp4[3]]] + _, p_val = fisher_exact(dp2x2) + sb = pval_to_phredqual(p_val) + if fields[7] == "": + info = [] + else: + info = fields[7].split(';') + info.append("DP=%d" % (dp)) + info.append("AF=%.6f" % (af)) + if isnan(faf): + info.append("FAF=NaN") + else: + info.append("FAF=%.6f" % (faf)) + if isnan(raf): + info.append("RAF=NaN") + else: + info.append("RAF=%.6f" % (raf)) + info.append("SB=%d" % (sb)) + info.append("DP4=%s" % (','.join([str(x) for x in dp4]))) + new_info = ';'.join(info) + fields[7] = new_info + out_vcf.write("%s\n" % ("\t".join(fields))) + in_vcf.close() + out_vcf.close() + + +if __name__ == "__main__": + annotateVCF(sys.argv[1], sys.argv[2], sys.argv[3])