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Items: 11

Search results: x Variables, w Analyses, x Documents, and z Datasets in x Studies
StudyEmbargo Release Details  ParticipantsType Of StudyLinksPlatform
phs000007.v30.p11
Framingham Cohort		Versions 1-30: passed embargo
VDAS15154 Longitudinal
HuGeneFocused50K_Affy
Mapping250K_Nsp
Mapping250K_Sty
Mapping50K_Hind240
Mapping50K_Xba240
phs000280.v5.p1
Atherosclerosis Risk in Communities (ARIC) Cohort		Versions 1-5: passed embargo
VDAS15678 Longitudinal, Cohort
phs000234.v2.p2
Group Health/UW Aging and Dementia eMERGE Study		Versions 1-2: passed embargo
VDAS3756 Case-ControlLinks
Human660W-Quad_v1_A
phs000219.v1.p1
GenADA/LONG/Imaging (Genetic Alzheimer's Disease Associations)		Version 1: passed embargo
VDAS1718 Case-ControlLinks
Mapping250K_Nsp
Mapping250K_Sty
phs000888.v1.p1
eMERGE Network Imputed GWAS for 41 phenotypes		Version 1: passed embargo
VDAS55029 Case-Control, CohortLinks
1000 Genomes
phs001584.v1.p1
eMERGE Network Phase III: HRC Imputed Array Data of 83,000+ Participants		Version 1: passed embargo
VDAS83717 Case-ControlLinks
Nimblegen Custom SeqCap
phs000126.v2.p1
CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD)		Versions 1-2: passed embargo
VDAS1991 Case-ControlLinks
HumanCNV370v1
phs000101.v5.p1
Genome-Wide Association Study of Amyotrophic Lateral Sclerosis		Versions 1-5: passed embargo
VDAS15480 Case-ControlLinks
HumanHap300v1.1
HumanHap250Sv1.0
HumanHap550v3.0
HumanHap550v1.1
Human610_Quadv1_B
iSelect Custom Panel
TruSeq Exome Enrichment Kit
HiSeq 2000
SureSelect
SeqCap EZ Human Exome Library v1.0
SeqCap EZ Human Exome Library v2.0
HumanOmniExpress-24 v1.0
HumanOmniExpress-24 v1.1
phs000006.v1.p1
NINDS Repository Motor Neuron Disease/ALS Study		Version 1: passed embargo
VDAS1790 Case SetLinks
phs001516.v1.p1
Phenotype Risk Score Study of Rare Variants		Version 1: passed embargo
VDAS21701 CohortLinks
Infinium HumanExome BeadChip
phs000090.v4.p1
GENEVA: The Atherosclerosis Risk in Communities (ARIC) Study		Versions 1-4: passed embargo
VDAS12771 Case-Control
AFFY_6.0
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