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vcf files modification before converting to BCF...

bioinformaticsbcftoolsvcf-variant-call-format

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Extract sample data from VCF files...

rbioinformaticsvcf-variant-call-format

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vcf to ped format: redefine non-dbSNPs...

bioinformaticsvcftoolsvcf-variant-call-format

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Parse VCF file's INFO field...

bashawksedbioinformaticsvcf-variant-call-format

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Using pyranges library, How to check if a chromosome position is contained in any interval?...

pythonbioinformaticsvcf-variant-call-formatpyranges

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vcf-consensus script error: The sequence N not found in the fasta file...

bioinformaticsvariantfastaconsensusvcf-variant-call-format

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