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

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    Sandhya Xirasagar

    Thank you for this document, this is helpful. t looks like the is only good for single sample calling. Do you plan to release a CNN tool coming for multi-sample gremlin variant calling?

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    Thank you for this great tool. I was wondering if the pre-trained architecture would be suitable for non-human data, or would it be better to stick to hard filtering?

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