Consortia
CSER
CSER
Overview
Studies
Workspaces
Terra Workspace
Study
Consent Code
Disease (indication)
Data Type
Study Design
Participants
AnVIL_CSER_CHARM_GRU
CSER: Exome Sequencing in Diverse Populations in Colorado and Oregon/CHARM Cancer Health Assessments Reaching Many
GRU
Hereditary Cancer Risk
Whole Exome
Clinical Trial
827
AnVIL_CSER_NYCKIDSEQ_GRU
CSER: Incorporating Genomics into the Clinical Care of Diverse NYC Children (NYCKidSeq)
GRU
Suspected Genetic Disorder
2 data types
Clinical Trial
449
AnVIL_CSER_NCGENES2_GRU
CSER: North Carolina Clinical Genomic Evaluation by Next-Gen Exome Sequencing 2
GRU
Suspected Genetic Disorder
Whole Exome
Clinical Trial
100
AnVIL_CSER_KidsCanSeq_GRU
CSER: Evaluating Utility and Improving Implementation of Genomic Sequencing for Pediatric Cancer Patients in the Diverse Population and Healthcare Settings of Texas: The KidsCanSeq Study
GRU
Cancer
2 data types
Case Set
623
AnVIL_CSER_NYCKIDSEQ_HMB
CSER: Incorporating Genomics into the Clinical Care of Diverse NYC Children (NYCKidSeq)
HMB
Suspected Genetic Disorder
2 data types
Clinical Trial
269
AnVIL_CSER_SouthSeq_GRU
CSER: South-Seq: DNA Sequencing for Newborn Nurseries in the South
GRU
Suspected Genetic Disorder
Whole Genome
Family/Twins/Trios
752
AnVIL_CSER_ClinSeq_GRU
The ClinSeq Project: Piloting Large-Scale Genome Sequencing for Research in Genomic Medicine
GRU
Healthy Adults
0
Case Set
0
AnVIL_CSER_P3EGS_GRU
CSER: Genomic Sequencing to Aid Diagnosis in Pediatric and Prenatal Practice: Examining Clinical Utility, Ethical Implications, Payer Coverage, and Data Integration in a Diverse Population
GRU
2 diseases
Whole Exome
2 study designs
534