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

Call input and runtime attributes evaluation failed for PairedFastQsToUnmappedBAM


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    George Grant


    Hi Ananya,

    This document should explain how to set up the inputs (and how the fastq files should be accessible).

    Hope that helps.

    - George


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