CSER
Terra Workspace | Study | Consent Code | Disease (indication) | Data Type | Study Design | Participants |
---|---|---|---|---|---|---|
AnVIL_CSER_CHARM_GRU | Unspecified | GRU | Hereditary Cancer Risk | Whole Exome | Clinical Trial | 827 |
AnVIL_CSER_NYCKIDSEQ_GRU | Unspecified | GRU | Suspected Genetic Disorder | 2 data types | Clinical Trial | 449 |
AnVIL_CSER_NCGENES2_GRU | Unspecified | GRU | Suspected Genetic Disorder | Whole Exome | Clinical Trial | 100 |
AnVIL_CSER_KidsCanSeq_GRU | Unspecified | GRU | Cancer | 2 data types | Case Set | 623 |
AnVIL_CSER_NYCKIDSEQ_HMB | Unspecified | 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 |