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

Errors about read group (RG) information Follow

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    Stephen Johnson

    Thank you for this example of how to use AddOrReplaceReadGroups! Would a specified RGPU also be a required for this to run?

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