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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
** How to generate filtered variant calls for SNPs
** How to generate filtered variant calls for SNPs
** Basic variant call file format (VCF)
** Basic variant call file format (VCF)
** How to visualize the variant calls to examine the variants at particular genomic positions
** How to examine the variants at particular genomic positions
** How to evaluate the quality of variant calls
** How to evaluate the quality of SNP calls
== GotCloud SnpCall Pipeline ==
== GotCloud SnpCall Pipeline ==
