Supporting Data for "Strelka2: Fast and accurate variant calling for germline and somatic sequencing applications"

Name: Supporting Data for "Strelka2: Fast and accurate variant calling for germline and somatic sequencing applications"
Creator: Scheffler, Konrad; Källberg, Morten; Bekritsky, Mitchell A; Kim, Yeonbin; Saunders, Christopher; Noh, Eunho; Kim, Sangtae; Beyter, Doruk; Chen, Xiaoyu; Krusche, Peter; L Halpern, Aaron
Published: 2018-05-03 00:00:00
License: 暂无描述

Figshare2018-05-03 更新2026-04-08 收录

下载链接：

https://figshare.com/articles/dataset/Supporting_Data_for_Strelka2_Fast_and_accurate_variant_calling_for_germline_and_somatic_sequencing_applications_/6203264/1

下载链接

链接失效反馈

官方服务：

资源简介：

This fileset includes supporting data files describing:<br>1. The SNV and Indel truth set used to evaluate accuracy on <i>in silico</i> mixtures of germline samples.- InSilicoMix_snvs.vcf.gz- InSilicoMix_indels.vcf.gz- InSilicoMix_falsePositiveRegions.bed.gz<br>2. The list of chromosomes included for analyses using the GRCh38+Decoy reference.- GRCh38DecoyCallableChroms.bed.gz

提供机构：

Scheffler, Konrad; Källberg, Morten; Bekritsky, Mitchell A; Kim, Yeonbin; Saunders, Christopher; Noh, Eunho; Kim, Sangtae; Beyter, Doruk; Chen, Xiaoyu; Krusche, Peter; L Halpern, Aaron

创建时间：

2018-05-01