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

🗓️ Mutect2 Webinar [Nov 17 2020] Follow

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    Patri ciabin

    In this webinar, you will learn about how Mutect2 works, and see an example of how to run it in the cloud on Terra.The webinar will cover somatic SNVs and Indels discovery using Mutect2 - a pipeline for calling somatic short mutations using local   spacebar clicker   assembly of haplotypes.Call somatic short mutations via local assembly of haplotypes. Short mutations include single nucleotide (SNA) and insertion and deletion (indel) alterations. Integrate your tools with the GDC and learn the SDK at our 'Integrating Analysis Tools with GDC' webinar. Dismiss. Skip Navigation. Login. Video Guides.

     
     
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