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

Picard LiftOverVCF 100.0000% of variants were not successfully lifted over

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    Gökalp Çelik

    HiNur Adlina Binti Mohd Affian

    Looks like your source vcf uses a reference genome that is not compatible with your liftover chain file. Can you check the chain file contents to see if it searches for contig names starting with chr from the source file?

    Regards. 

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