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

emit-ref-confidence error

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    Genevieve Brandt (she/her)

    Hi Camila Martínez Avila,

    Thanks for writing in! The command you mentioned is useful for viewing the read groups in your bam file. This makes sure that you have read groups in your file and also tells you the sample name(s) in your file.

    If there is nothing output from the command, you probably do not have read groups in your bam file. Check out our article on read groups and another article detailing how to add them to your bam file.

    Let me know if this solves your issue or if you have further questions.

    Best,

    Genevieve

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    Camila Martínez Avila

    Thanks a lot!
    I'm adding the information to my samples and I haven't had problems with the AddOrReplaceReadGroups function. I'm going to try running HaplotypeCaller on this fixed files and hope not to get any error.

    Again, than you very much.

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    Genevieve Brandt (she/her)

    Great! Let me know if the error comes up and I can help if so.

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