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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    Gökalp Çelik

    Hi Nikee Shrestha

    Yes you can. You can use the tool SelectVariants and use -L parameter to indicate which chromosomes to include and you will get a subset of variants for your selected chromosomes. 

    Regards. 

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