Mercurial > repos > erasmus-medical-center > hla_dq
view hla_dq.py @ 1:4fc47a3ff9e8 draft default tip
planemo upload for repository https://github.com/ErasmusMC-Bioinformatics/galaxytools-emc/tree/master/tools/hla_dq commit 3f631031b57350f0437e90e4de3352725bb84716
author | erasmus-medical-center |
---|---|
date | Wed, 30 May 2018 09:21:15 -0400 |
parents | 10a407fb5072 |
children |
line wrap: on
line source
#!/usr/bin/env python ''' Given HLA-A and HLA-B genes annotated with BLAST IMGT/HLA database genotypes, determine associated serotypes DQA1 | DQB1 | type -------------------- 02:01| 02:02| DQ2.2 03:03| 02:02| DQ2.3 05:01| 02:01| DQ2.3 03:01| 03:02| DQ8 03:02| 03:02| DQ8 03:03| 03:02| DQ8 Annotations are of form DQ[A|B]1*xx:yy[:zz[:vv]] where xx:yy is of interest. Example: "HLA:HLA11066 DQA1*01:05:02 768 bp" ''' import argparse import itertools def to_matrix(l, n): return [l[i:i+n] for i in range(0, len(l), n)] def get_list_of_associated_types(filename, column): with open(filename) as f: contents = f.readlines() return [':'.join(line.split('\t')[column-1].split(' ')[1] .split('*')[1].split(':')[0:2]) for line in contents[1:]] def get_associations(typesA, typesB): ''' Given list of genotype annotations (e.g. DQA1*02:01..) from A and B, determine possible associated serotypes ''' ''' each combination of DQA1,DQB1,type ''' associated_combinations = [ ['02:01', '02:02', ' DQ2.2 (02:01-02:02)'], ['03:03', '02:02', ' DQ2.3 (03:03-02:02)'], ['05:01', '02:01', ' DQ2.5 (05:01-02:01)'], ['03:01', '03:02', ' DQ8 (03:01-03:02)'], ['03:02', '03:02', ' DQ8 (03:02-03:02)'], ['03:03', '03:02', ' DQ8 (03:03-03:02)']] return [a[2] for a in associated_combinations if a[0] in typesA and a[1] in typesB] if __name__ == "__main__": parser = argparse.ArgumentParser() parser.add_argument('-A', required=True, action='append', help='BLAST hits A gene') parser.add_argument('-B', required=True, action='append', help='BLAST hits B gene') parser.add_argument('-c', '--column', default=5, type=int, help='Column number containing the BLAST annotation') args = parser.parse_args() # TODO: QC check that file A contains DQA1 annotations and # B file contains DQB1 annotations? # find possible associated types, for all combinations of alleles typesA = [get_list_of_associated_types(A, args.column) for A in args.A] typesB = [get_list_of_associated_types(B, args.column) for B in args.B] associations = [get_associations(c[0], c[1]) for c in itertools.product(typesA, typesB)] associations = to_matrix(associations, len(args.B)) # write output table header = '\t'+'\t'.join(['B'+str(i+1) for i in range(0, len(args.B))])+'\n' bcount = 0 with open('results.tsv', 'w') as outfile: outfile.write(header) for line in associations: bcount += 1 outfile.write( 'A' + str(bcount) + '\t' + '\t'.join([';'.join(sorted(set(l))) if l else ' -' for l in line])+'\n')