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, 23:09, 14 June 2014
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| ** 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 == |