This is a test version of Biostars. For the public version, visit https://www.biostars.org.
Variant calling on aligned BAM files of WES

Could someone help in identifying SNVs in aligned BAM files alone? The index files provided are not .bai format. I know i need to use callVariants function, but the documentation is not clear on how to use this for WES. The exact code snippets would be better.

variant calling rna-seq

Creating a .bai index is as simple as samtools index your.bam.

I know i need to use callVariants function

What tool is this function from?

The exact code snippets would be better

This applies to original question as well.

0 answers

No answers yet.

Log in to answer this question.