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

FastqToSam error when using paired reads

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    Gökalp Çelik

    Hi malonzm1

    Can you check the number of reads in each pair? Those 2 should match if not then I have more suggestions to add.

     

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