3,045
edits
Changes
From Genome Analysis Wiki
Jump to navigationJump to searchSeqShop: Variant Calling and Filtering for SNPs Practical, June 2014 (view source)
Revision as of 23:09, 14 June 2014
, 23:09, 14 June 2014→Goals of This Session
== Goals of This Session ==
== Goals of This Session ==
* What we want to learn
* What we want to learn
** How to generate filtered variant calls for SNPs
** How to generate filtered variant calls for SNPs from BAMs
** Basic variant call file format (VCF)
** Basic variant call file format (VCF)
** How to examine the variants at particular genomic positions
** How to examine the variants at particular genomic positions
