NHGRI Analysis Visualization and Informatics Lab-space

CMG

The Centers for Mendelian Genomics is a multi-center collaboration aimed at identifying the genes responsible for Mendelian phenotypes by whole exome and whole genome sequencing.

Consent Codes

DS-NIC-EMP-LENF, HMB-NPU, DS-HFA, HMB-MDS, TBD, HMB, DS-CVD-MDS, DS-NEURO-GSO-MDS, DS-BFD-MDS, DS-BDIS, DS-EP, GRU, GRU-IRB, DS-NBIA, NA, Consortia Access Only, HMB-IRB, DS-RARED, HMB-IRB-NPU, DS-MC, DS-CSD-MDS, DS-BAV-IRB-PUB-PD, HMB-GSO

Diseases

Mendelian disorders, Rare Disease

Study Design

Parent-Offspring Trios, TBD, Family/Twins/Trios, Mendelian

Data Types

Whole Genome, Exome, TBD

Subjects

2,580