Created
October 9, 2017 07:50
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Extension of MuPeXI to all Variant Callers
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--- a/MuPeXI.py | |
+++ b/MuPeXI.py | |
@@ -466,6 +466,7 @@ def create_vep_compatible_vcf(vcf_file, webserver, keep_tmp, outdir, file_prefix | |
def extract_allele_frequency(vcf_sorted_file, webserver, variant_caller): | |
print_ifnot_webserver('\tExtracting allele frequencies', webserver) | |
allele_fractions = defaultdict(dict) | |
+ freq_colms=set(["AF","FREQ","FA"]) | |
if not variant_caller in ('MuTect','MuTect2'): | |
allele_fractions = None # no variant caller detected | |
@@ -483,10 +484,18 @@ def extract_allele_frequency(vcf_sorted_file, webserver, variant_caller): | |
if not len(reference_allele) == len(altered_allele): | |
altered_allele = altered_allele[1:] if len(reference_allele) < len(altered_allele) else altered_allele | |
altered_allele = '-' if len(reference_allele) > len(altered_allele) else altered_allele | |
- if variant_caller == 'MuTect': | |
- allele_fraction = columns[9].split(':')[format_fields.index('FA')].strip() # GT:AD:BQ:DP:FA | |
- elif variant_caller == 'MuTect2': | |
- allele_fraction = columns[9].split(':')[format_fields.index('AF')].strip() # GT:AD:AF:ALT_F1R2:ALT_F2R1:FOXOG:QSS:REF_F1R2:REF_F2R1 | |
+ freq_col=freq_colms.intersection(format_fields) | |
+ if(len(freq_col)==0): #freebayes | |
+ c9=columns[9].split(':') | |
+ AO=c9[format_fields.index('AO')] | |
+ if("," in AO): | |
+ AO=AO.split(',')[0] | |
+ AO=float(AO) | |
+ DP=float(c9[format_fields.index('DP')]) #should use RO, but that is often zero near indels | |
+ allele_fraction=str(AO/(AO+DP)) | |
+ else: | |
+ field_idx=format_fields.index(freq_col.pop()) | |
+ allele_fraction = columns[9].split(':')[field_idx].strip() # GT:AD:BQ:DP:FA | |
ID = '{chromosome}_{genomic_position}_{altered_allele}'.format( | |
chromosome = chromosome, | |
genomic_position = genomic_position if not altered_allele == '-' else int(genomic_position) + 1, |
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