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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

How can I resume a failed/interrupted Mutect2 tumor-only mode run?

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    Genevieve Brandt (she/her)

    Thank you for your post, Anna Darlene van der Heiden! I want to let you know we have received your question and will be moving it to the Community Discussions -> General Discussion topic, as the Other topic is for reporting bugs and issues with GATK.

    We'll get back to you if we have any updates or follow up questions. Please see our Support Policy for more details about how we prioritize responding to questions. 

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    Genevieve Brandt (she/her)

    Hi Anna Darlene van der Heiden,

    Unfortunately there is no way to resume your Mutect2 run. If there are samples that are large and having a difficult time finishing, you can break up your analysis by intervals and then merge the output VCFs with MergeVCFs: https://gatk.broadinstitute.org/hc/en-us/articles/5358883370011-MergeVcfs-Picard-.

    Let me know if you have any other questions.

    Best regards,

    Genevieve

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    Genevieve Brandt (she/her)

    Hi Anna,

    We haven't heard from you in a while so we're going to close out this ticket in our system. If you still require assistance, simply respond to this thread and we'll be happy to pick up where we left off!

    Kind regards,

    Genevieve​

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