Genomic variants (CHRIS baseline)
md_x0_0026
Genomic variants
Genotype array (CHRIS baseline)
Genotypes from genotyping on the Illumina Human Omni Microarray platform
4 variables.
0 sub-modules.
Public imputation panels (CHRIS baseline)
Public imputation panels
2 variables.
0 sub-modules.
Whole-exome sequencing (CHRIS baseline)
Whole-exome sequencing
2 variables.
0 sub-modules.
Whole-exome sequencing imputation (CHRIS baseline)
Genotypes including genotypes imputed from the CHRIS WES dataset
2 variables.
0 sub-modules.
No variables.
No documents.
No groups.