NHGRI Analysis Visualization and Informatics Lab-space

Study

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Baylor Hopkins Center for Mendelian Genomics (BH CMG)

CMGphs000711.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.

Stats

2Cohorts
2,861Samples
876Participants
36.10 TBSize

Summary

Consent CodesHMB-IRB-NPU, HMB-NPU
DiseasesMendelian disorders
AccessControlled Access
Study DesignTBD
Data TypesExome

Applying For Access

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Terra Workspaces

This study has been divided into the following workspaces by consent codes and optionally the originating laboratory.

Terra Workspace NameConsent CodeDiseaseAccessStudy DesignData TypeSamplesParticipantsSize (TB)
AnVIL_CMG_BaylorHopkins_HMB-IRB-NPU_WESHMB-IRB-NPUMendelian disordersTBDExome8074384.87
AnVIL_CMG_BaylorHopkins_HMB-NPU_WESHMB-NPUMendelian disordersTBDExome2,05443831.24