CHRIS Portal - Whole-exome sequencing (CHRIS baseline) module

Whole-exome sequencing (CHRIS baseline)

md_x0_0029

Whole-exome sequencing

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WES variant calls GRCh37 (vcf)

WES variant calls GRCh37 (vcf)

WES variant calls GRCh38, lifted from GRCh37 (vcf)

WES variant calls GRCh38, lifted from GRCh37 (vcf)

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Show all variables of Whole-exome sequencing (CHRIS baseline)