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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

GATK GRCh38 Reference

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    Gökalp Çelik

    Hi Yasir K

    Currently we do not support AWS platforms therefore we cannot help on the availability of resources within AWS. Our original hg38 contained all unlocalized contigs, alt contigs and HLA sequences as a whole and our recommendation followed with bwa mem and using alt-aware mapping. However we recognized that alt contig handling is not optimal in most cases therefore it is not practical to continue using that reference any further. Our DRAGEN-GATK FE workflows recommend using the masked hg38 recommendation from Illumina which can be obtained by masking the reference genome during index creating step if DRAGMAP is used as mapper or can be masked by other tools before index creation by BWA.

    You may be able to reach the fasta sequence and masking regions from the link below

    https://console.cloud.google.com/storage/browser/gcp-public-data--broad-references/hg38/v0/dragen_reference 

    I hope this helps.

    Regards. 

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