Jump to: Authorized Access | Attribution | Authorized Requests

Study Description

The Centers for Mendelian Genomics project uses next-generation sequencing and computational approaches to discover the genes and variants that underlie Mendelian conditions. By discovering genes that cause Mendelian conditions, we will expand our understanding of their biology to facilitate diagnosis and new treatments.

Authorized Access
Publicly Available Data
Molecular Data
TypeSourcePlatformNumber of Oligos/SNPsSNP Batch IdComment
Whole Exome Sequencing Illumina HiSeq 2000 N/A N/A v1, v2, v3
Whole Exome Sequencing Illumina HiSeq 2500 N/A N/A TruSeq Rapid PE
Exome Capture Roche NimbleGen HGSC-Core; HGSC-VCRome N/A N/A Custom
Exome Capture Agilent SureSelect HumanAllExonV4_51MbKit_S03723314 N/A N/A
Exome Capture Agilent SureSelect HumanAllExonV5Clinical_S06588914 N/A N/A
Selected Publications
Diseases/Traits Related to Study (MeSH terms)
Authorized Data Access Requests
Study Attribution
  • Sequencing Centers
    • Baylor Hopkins Center for Mendelian Genomics. Baylor College of Medicine, Houston, TX, USA.
  • Principal Investigators
    • David Valle, MD. Johns Hopkins School of Medicine, Baltimore, MD, USA.
    • James Lupski, MD, PhD. Baylor College of Medicine, Houston, TX, USA.
  • Funding Sources
    • 1U54HG006542. National Human Genome Research Institute and National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.