GATCI_WGS_mutect.2 - samples
收藏NIAID Data Ecosystem2026-03-13 收录
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资源简介：
Sequence data in fastq format was aligned to the GRCh38 reference genome with BWA-MEM and preprocessed with GATK for indel realignment and base quality score recalibration. Aligned sequence was analyzed with MuTect to generate somatic variant calls. Variant calls are in VCF format. In total, there are 60 tumour samples from 38 patients, all with matched normal. Further details can be found in the vcf headers.EGA dataset EGAD00001005822
创建时间：
2022-09-01
