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Baylor Hopkins Center for Mendelian Genomics (BH CMG)

phs000711.v7.p2dbGapdbGap FHIR

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.

Summary

PlatformsAnVIL
Consent CodesNRUP, HMB-NPU, HMB-IRB-NPU
Focus / DiseasesMendelian Conditions
Study DesignMendelian
Data TypesSNP Genotypes (NGS), SNP/CNV Genotypes (NGS), WXS
Subjects2,445