Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

GenotypeGVCF - missed SNP ID

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    Louis Bergelson

    Hi Salma H. Elaksher,

    I think you're saying that your output vcf is missing rsID tags for known variants? 

    If you want those added to your file when doing GenotypeGvcfs, you have to include the --dbsnp argument, and a dbSnp vcf with the tags you want to use.  Otherwise it will not be populated.  

    Since you've already genotyped these, you can annotate the existing vcf by running it through VariantAnnotator with the --dbsnp argument.

    I hope that helps. 

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