Changes between Version 2 and Version 3 of AlleleCounting
- Timestamp:
- Aug 24, 2011 10:52:06 AM (13 years ago)
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AlleleCounting
v2 v3 3 3 This method can be used to create a SNP list across multiple samples and establish the allele count for each variant. 4 4 5 == Step 1: Merge samples vcf using GATK CombineVariants ==5 == Step 1: Merge samples vcf using GATK !CombineVariants == 6 6 7 7 Merge sample vcf using [http://www.broadinstitute.org/gsa/wiki/index.php/CombineVariants CombineVariants] 8 8 9 Semi-code: 9 10 {{{