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Some row names are dbSNP IDs, which makes it impossible to obtain chromosome, position or reference information the way it is done in the vcf.to.sigs.input function.
Hi,
when processing VCF files with partially (or fully) annotated ID field using the readGT function, what you get back is a matrix looking like this:
Some row names are dbSNP IDs, which makes it impossible to obtain chromosome, position or reference information the way it is done in the vcf.to.sigs.input function.
Is there a reason other than readGT being lightweight, that a more general solution like this below is not used?
Thanks for all the work!
Marko
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