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dbGaP

The database of Genotypes and Phenotypes (dbGaP) was developed to archive and distribute the data and results from studies that have investigated the interaction of genotype and phenotype in Humans.

Latest Studies

Study Embargo Release Details Participants Type Of Study Links Platform
phs001651.v1.p1
Characterization of Squamous Cell Lung Cancers from Appalachian Kentucky

Version 1:
V D A S 51 Case Set Links
Nextera Rapid Capture Exome
phs001194.v2.p2
Pediatric Cardiac Genomics Consortium (PCGC) Study
Versions 1-2: passed embargo
V D A S 9463 Parent-Offspring Trios, Cohort Links
HiSeq X Ten
HiSeq 2000
xGen Exome Research Panel v1.0
SeqCap EZ Accessory Kit V2
SeqCap EZ MedExome Kit
SureSelect Targeted Enrichment
HumanOmni1-Quad BeadChip
HumanOmni2.5-8v1_B
HumanOmni2.5-8 (Omni2.5)
phs001619.v1.p1
Genetic Analysis of Patients with Inherited Retinal Dystrophies (IRDs)

Version 1:
V D A S 9 Case-Control Links
Illumina HiSeq X 10
phs000653.v3.p1
Epi4K: Gene Discovery in 4,000 Epilepsy Genomes
Versions 1-2: passed embargo
Version 3:
V D A S 2186 Parent-Offspring Trios, Multiplex Families, Case-Control Links
TruSeq Exome Enrichment Kit
Kapa Hyper Library Preparation Kit
SeqCap EZHuman Exome Library v3.0
TruSeq Exome Library Prep Kit
KAPA Library Preparation Kit
SeqCap EZ Exome v3
phs001575.v1.p1
Assessment of Neurological Deterioration in Subjects with LINCL
Version 1: passed embargo
V D A S 42 Longitudinal Links
List Top Level Studies
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