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Supporting Data for "Strelka2: Fast and accurate variant calling for germline and somatic sequencing applications"
dataset
posted on 2018-05-01, 17:18 authored by Sangtae KimSangtae Kim, Konrad Scheffler, Aaron L Halpern, Mitchell A Bekritsky, Eunho Noh, Morten Källberg, Xiaoyu Chen, Yeonbin Kim, Doruk Beyter, Peter Krusche, Christopher SaundersChristopher SaundersThis fileset includes supporting data files describing:
1. The SNV and Indel truth set used to evaluate accuracy on in silico mixtures of germline samples.
- InSilicoMix_snvs.vcf.gz
- InSilicoMix_indels.vcf.gz
- InSilicoMix_falsePositiveRegions.bed.gz
2. The list of chromosomes included for analyses using the GRCh38+Decoy reference.
- GRCh38DecoyCallableChroms.bed.gz
