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

A USER ERROR has occurred: Badly formed genome unclippedLoc

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    Genevieve Brandt (she/her)

    Hi suzy_bunters,

    Could you try only specifying that interval in the -XL parameter in the format chr20:1-100? To check if the issue is with the interval or the submitted format.

    Genevieve

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    suzy_bunters

    Hi Genevieve, it's now running in the format you suggested, thank you. Each job I submit to the cluster sits in a queue for hours, so testing different formats was taking a long time! 

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    Genevieve Brandt (she/her)

    Hi suzy_bunters, if that runs fine, then the issue must be with the format of the file. For a workaround, you can submit the file without that line and then use another -XL argument to use the format I recommended above. It is fine to submit multiple interval arguments.

    Best,

    Genevieve

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