Hi all, I am trying to embed SNPs directly in a sam file for simulation purposes, i.e for a given set of genomic positions, to identify the reads the cover them and to overwrite values (nucleotides) on the positions on the reads that correspond to the input genomic positions.
Any ideas on how to do this ? in particular in R?
Thanks,
Yiannis
Any ideas on how to do this ? in particular in R?
Thanks,
Yiannis
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