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

Intrerval list from bed file

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    Pamela Bretscher

    Hi Priyadarshini Thirunavukkarasu,

    It looks like this is most likely due to an incompatibility in the naming of the chromosomes between your bed file and dictionary file. Could you take a look at this document about incompatibilities in input files and check to make sure that the chromosome naming matches between your files?

    Kind regards,

    Pamela

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