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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

Install GATK version 4.1.0.0 using Conda.

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    Gökalp Çelik

    Hi dongju

    Since GATK 4.1.0.0 is an earlier version conda dependencies might have changed and some of the dependencies are even not available in the conda repository. Can you try installing a recent version of GATK like 4.3.0.0 or 4.4.0.0?

    Here is the versions of setuptools as an example from the conda repository. And as you can see 36.4 is not there anymore. You may still use the docker version of 4.1.0.0 which already has all the conda environment dependencies installed properly. 

    Another solution would be to modify the yml file to point to the conda-forge channel for packages but this would be totally experimental and unsupported. Any non-matching package version installed might cause errors or calculation differences among tools. Our actual suggestion would still be using the latest GATK 4.4.0.0 version or the docker version of 4.1.0.0. 

    I hope this helps. 

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    dongju

    Thank you for the helpful response. I have installed GATK version 4.4.

    Now, I want to use GATK CreateSomaticPanelOfNormals with multiple VCF files as input.

    How can I use the -V option to achieve this?

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    Gökalp Çelik

    Hi dongju

    A sample workflow is explained here in the following link. You need to combine your variants into a GenomicsDB format and use that as an input if you have multiple vcf files for your PoN. 

    https://gatk.broadinstitute.org/hc/en-us/articles/13832769396635-CreateSomaticPanelOfNormals-BETA- 

    I hope this helps. 

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    dongju

    I appreciate your time:)

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