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

CombineGVCFs Follow

2 comments

  • Avatar
    maryam montazeri

    Hi. Thanks for providing your good software.
    I had a question, why the output of combinegvcf does not have a sample name and has a column called label?
    Please advise.
    Thanks

    0
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  • Avatar
    maryam montazeri

    Hi. Thanks for providing your good software.
    I had a question, why the output of combinegvcf does not have a sample name and has a column called label?
    Please advise.
    Thanks

    0
    Comment actions Permalink

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