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nickloman/misc-genomics-tools
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Some scripts for handling multiple VCF files run e.g. python ../scripts/index_multiple_vcf.py variant_files bcf_files results.pickle python ../scripts/tabulate_multiple_vcf.py results.pickle > results.fna Assumes there is a file called 'variant_files' which lists all the VCF files e.g. NC_002755_K7_ilmn_bwa.vcf NC_002755_K7_pgm.noindel.vcf NC_002755_K8_ilmn_bwa.vcf And a file called bcf_files which is a list of display identifiers and BCF files (tab-separated), e.g. K7_ilmn NC_002755_K7_ilmn_bwa.all.bcf.gz K7_pgm NC_002755_K7_pgm.all.bcf.gz K8_ilmn NC_002755_K8_ilmn_bwa.all.bcf.gz
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assorted scripts for doing genomics
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