Version 3 (modified by 13 years ago) (diff) | ,
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Allele Counting SOP
This method can be used to create a SNP list across multiple samples and establish the allele count for each variant.
Step 1: Merge samples vcf using GATK CombineVariants
Merge sample vcf using CombineVariants
Semi-code:
cd ~/projects/yourproject/rawdata java -Xmx2g -jar /target/gpfs2/gcc/tools/GATK-1.1-23-g8072bd9/Sting/dist/GenomeAnalysisTK.jar\ -T CombineVariants\ -B:sample1,VCF sample1.all.snp.txt.vcf\ -B:sample2,VCF sample2.all.snp.txt.vcf\ -B:sample3,VCF sample3.all.snp.txt.vcf\ -B:sample4,VCF sample4.all.snp.txt.vcf\ -R /target/gpfs2/gcc/resources/hg19/indices/hg19.fa\ -o union.vcf
Step 2: count alleles using VCF tools
Count allele using VCFtools. Semicode:
TODO