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Revision as of 10:23, 22 May 2015
, 10:23, 22 May 2015→Annotation / Lookup against dbSNP
If you want to add rsIDs to your variant files, you can do this by running the following command
If you want to add rsIDs to your variant files, you can do this by running the following command
$HK/vcf-add-rsid -vcf $OUT/vcfs/chr1/chr1.filtered.vcf.gz --db $HK/../data/dbSNP.b138/dbsnp_138.b37.vcf.gz --out $OUT/vcfs/chr1/chr1.filtered.rsid.vcf.gz
$HK/vcf-add-rsid -vcf $OUT/vcfs/chr1/chr1.filtered.vcf.gz --db $HK/../data/dbsnp_142.b37.vcf.gz --out $OUT/vcfs/chr1/chr1.filtered.rsid.vcf.gz
If you want to run this command across all chromosomes in parallel, you can use the special script run-command-wgs
If you want to run this command across all chromosomes in parallel, you can use the special script run-command-wgs
