5 research outputs found
Strelka2: Fast and accurate variant calling for clinical sequencing applications
No full textStrelka2 poster for CSHL Genome Informatics 201
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree
No full textSupporting Data for "Strelka2: Fast and accurate variant calling for germline and somatic sequencing applications"
No full textThis fileset includes supporting data files describing:<div><br></div><div>1. The SNV and Indel truth set used to evaluate accuracy on <i>in silico</i> mixtures of germline samples.</div><div>- InSilicoMix_snvs.vcf.gz</div><div>- InSilicoMix_indels.vcf.gz</div><div>- InSilicoMix_falsePositiveRegions.bed.gz</div><div><br></div><div>2. The list of chromosomes included for analyses using the GRCh38+Decoy reference.</div><div>- GRCh38DecoyCallableChroms.bed.gz</div
