hi All
i'm new in this NGS "neighborhood", and wondering ig anyone can guide me on how to use the variant calling in VarScan with seq data that comes with Phred score of 64 ?
according to their documentation the software works with sanger scores (phred33), so i have to make the adjusment myself.
any help will be appreciated :-)
Moran
i'm new in this NGS "neighborhood", and wondering ig anyone can guide me on how to use the variant calling in VarScan with seq data that comes with Phred score of 64 ?
according to their documentation the software works with sanger scores (phred33), so i have to make the adjusment myself.
any help will be appreciated :-)
Moran
Comment