The Variant Call Format (VCF) specifies the format of a text file used in bioinformatics for storing gene sequence variations.
I have a question about extracting a part of a string. For example I have a string like this: a &…
r regex string bioinformatics vcf-variant-call-formatI am working with PLINK to analyse genome-wide data. Does anyone know how to remove duplicated SNPs?
bioinformatics vcf-variant-call-format bcftoolsI am trying to convert a .vcf file to a .ped file using plink. I have read some manuals and …
bioinformatics vcftools vcf-variant-call-formatI have a large Variant Call format (VCF) file (> 4GB) which has data for several samples. I have browsed …
r bioinformatics vcf-variant-call-formatI have this VCF format file, I want to read this file in R. However, this file contains some redundant …
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