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Important notice: NIH has established a collection of dbGaP samples designated as appropriate for general research use (GRU) by submitting institutions, which indicates that there are no further limitations on secondary research use beyond those outlined in the Genomic Data User Code of Conduct. For details, visit the collection's page.
Search results: x Variables, w Analyses, x Documents, and z Datasets in x Studies
StudyEmbargo Release Details  ParticipantsType Of StudyLinksPlatform
phs000790.v1.p1
Comparative Analysis of Primary and Metastatic Colorectal Cancer

Version 1:
VDAS4 CohortLinks
HiSeq 2000
phs000848.v1.p1
Autosomal recessive TPP2 mutations cause a new human immunodeficiency

Version 1: 2015-12-16
VDAS3 Case-ControlLinks
Genome Analyzer IIX
phs000842.v1.p1
PediGFR
Version 1: passed embargo
VDAS1572 Multicenter, Prospective, Observational, CohortLinks
HumanOmni2.5-Quad
phs000007.v25.p9
Framingham Cohort
Versions 1-22: passed embargo
Version 23: 2015-04-25
Version 24: 2015-09-25
Version 25: 2015-12-23
VDAS15173 LongitudinalLinks
HuGeneFocused50K_Affy
Mapping250K_Nsp
Mapping250K_Sty
Mapping50K_Hind240
Mapping50K_Xba240
phs000825.v1.p1
Whole Genome Sequencing of HUES63 and HUES64
Version 1: passed embargo
VDAS2 Control SetLinks
HiSeq 2000
HiSeq 2500
phs000821.v1.p1
DNA Methylation age and mortality in the Lothian Birth Cohorts

Version 1: 2015-11-12
VDAS1366 Longitudinal CohortLinks
450K Infinium Methylation
phs000811.v1.p1
Comparison of custom capture for targeted next generation DNA sequencing
Version 1: passed embargo
VDAS10 Mixed, Cross-Sectional, Tumor vs. Matched-NormalLinks
MiSeq
phs000809.v1.p1
Autosomal recessive PGM3 mutations cause a new Congenital Disorder of Glycosylation
Version 1: passed embargo
VDAS8 Parent-Offspring TriosLinks
HiSeq 2000
phs000431.v2.p1
IgA Nephropathy GWAS (IGANGWAS)
Version 1: passed embargo
Version 2:
VDAS3617 Case-ControlLinks
HumanHap550v3.0
Human610_Quadv1_B
HumanOmni1-Quad_v1-0_B
phs000360.v2.p1
eMERGE Network Combined Dataset

Version 1: 2015-02-27
Version 2: 2015-02-27
VDAS18663 Case-ControlLinks
Human660W-Quad_v1_A
Human1M-Duov3_B
phs000153.v8.p7
Framingham SHARe Social Network
Versions 1-8: passed embargo
VDAS15173 LongitudinalLinks
phs000018.v2.p1
Search for Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (GoKinD study participants), GAIN
Versions 1-2: passed embargo
VDAS1972 Case-ControlLinks
Mapping250K_Nsp
Mapping250K_Sty
phs000798.v1.p1
Performance Characteristics of Selective Targeted Enrichment in Genetic Diagnostic Testing

Version 1: 2015-05-26
VDAS4 Control SetLinks
HumanOmni2.5-8 (Omni2.5)
SureSelect Human All Exon V5+UTR
HiSeq 2000
Custom SureSelect targeted enrichment GEDi capture kit
HiSeq 2000
phs000797.v1.p1
CTLA4 haploinsufficiency and immune dysregulation

Version 1: 2015-10-24
VDAS5 Case SetLinks
SureSelect 38Mb
SureSelect Human All Exon v3 - 50Mb
HiSeq 2500
SOLiD Next-Generation Sequencing
phs000794.v1.p1
Longitudinal Genome-Wide Analysis of Patients with Chronic Lymphocytic Leukemia

Version 1:
VDAS12 LongitudinalLinks
HiSeq 2000
phs000793.v1.p1
Paired AML Epigenetics Study on Clonality
Version 1: passed embargo
VDAS18 CohortLinks
EZ DNA Methylation Kit
phs000792.v1.p1
Oncogenomics of Malignant Peripheral Nerve Sheath Tumors
Version 1: passed embargo
VDAS18 Case SetLinks
GenomeWideSNP_6
HiSeq 2500
HiSeq 2500
phs000785.v1.p1
Sequencing Analysis of Cutaneous Squamous Cell Carcinoma

Version 1:
VDAS210 CohortLinks
OncoScan FFPE Assay Kit
SeqCap EZ Human Exome Library v2.0
SeqCap EZ Choice Library
phs000784.v1.p1
Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Version 1: passed embargo
VDAS1675 Family, InterventionalLinks
AFFY_6.0
phs000783.v1.p1
Gene Mutation and Rescue in Human Congenital Diaphragmatic Hernia (CDH)

Version 1:
VDAS275 CohortLinks
HiSeq 2000
SeqCap EZ Human Exome Library v2.0

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