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christianparobek edited this page Dec 10, 2014
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I will document my analysis through this wiki. The associated scripts (and results?) will be kept in this repo.
###Steps to good SNP-call data:
- variantCalling - documented as part of the gatk_pipeline repo.
- weakestLinks - remove the lowest-coverage samples prior to downstream analysis. Gives us a shot at getting full haplotypes for all SNPs.
- variantFiltering - modeled loosely after Manske et al.
###Population Differentiation:
-
vcf2structure - VCF file format must be converted to
STRUCTURE
format for bothSTRUCTURE
andadegenet
analysis. structure
adegenet
- recombination
- Derrick's dupFinder