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DNA
(36901)
LCL
(22832)
Fibroblast
(4834)
Somatic cell hybrid
(320)
iPSC
(236)
Plasmid
(164)
mESC
(86)
High Molecular Weight DNA
(77)
Smooth muscle
(61)
Amniotic fluid-derived cell line
(60)
Endothelial
(47)
Melanocyte
(35)
96 well plate of DNA samples
(34)
Keratinocyte
(33)
Adipose stromal cell
(29)
Preprocessed DNA
(20)
Tumor-derived cell line
(16)
Epithelial
(15)
Neuronally-derived
(13)
Collection of iPSC
(8)
Hybridoma
(7)
Myeloma
(7)
Antibodies
(5)
Chorionic villus-derived cell line
(4)
Mesothelial
(4)
Protein
(4)
Erythroleukemic cell line
(2)
Kidney-derived cell line
(2)
aging mapping panel
(2)
human variation panel
(2)
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(1)
Microcell hybrid
(1)
hybrid mapping panel
(1)
hybrid regional mapping panel
(1)
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B-Lymphocyte
(22899)
LCL
(18578)
Whole Blood
(14986)
Fibroblast
(1614)
Skin, Arm
(1073)
Skin, Unspecified
(496)
Somatic cell hybrid
(243)
Skin, Skin
(233)
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(125)
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(105)
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(66)
Skin, Ear
(65)
Amniotic fluid
(59)
Aorta, thoracic
(57)
Blood
(42)
Skin, Abdomen
(32)
Amniotic fluid-derived cell line
(23)
Stem cell
(16)
Brain striatum
(13)
Fetal, Unspecified
(12)
Skin, Leg
(12)
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(12)
Trachealis muscle
(12)
Vein, iliac
(11)
Gonad, Gonad
(10)
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(10)
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(10)
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(10)
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(9)
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(9)
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(9)
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(9)
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(8)
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(8)
Whole embryo, Embryo
(8)
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(7)
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(7)
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Conjunctiva, Conjunctiva
(5)
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(5)
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Chorionic villus-derived cell line
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(3)
Tumor-derived cell line
(3)
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(2)
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(2)
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(2)
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Endometrial, Uterus
(2)
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(2)
Kidney
(2)
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Mesothelial
(2)
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(2)
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(2)
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(1)
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(1)
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(1)
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(1)
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Endothelial
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Ewing sarcoma
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Fetal, Arm
(1)
Heart, Unspecified
(1)
Hydatidiform mole
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NINDS Repository
(33362)
NIGMS Human Genetic Cell Repository
(18350)
NHGRI Sample Repository for Human Genetic Research
(7438)
NIA Aging Cell Culture Repository
(4220)
AREDS2
(1889)
Autism
(358)
HD Community Biorepository
(184)
Centers for Disease Control and Prevention Repository
(27)
Allen Cell Collection
(21)
Orphan Disease Center
(15)
Human Reference Genetic Material Repository
(1)
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(348)
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Not Reported
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(28)
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(10)
Korean
(6)
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(3)
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(3)
Affected:
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Yes
(39301)
No
(9795)
Unknown
(3151)
At Risk
(2878)
Mutation Data Available:
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N
(59753)
Y
(6064)
No
(48)
Age at Sampling (Years):
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55-64
(9143)
45-54
(8069)
65-74
(8068)
35-44
(5718)
75-89
(5286)
5-14
(4699)
25-34
(4230)
15-24
(4084)
0-4
(3748)
90-99
(713)
100+
(229)
Collection:
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Cerebrovascular Disease
(13965)
Heritable Diseases
(11735)
Parkinsonism
(8456)
NHGRI Sample Repository for Human Genetic Research
(7438)
Motor Neuron Disease
(5558)
Epilepsy
(3597)
Chromosome Abnormalities
(2932)
Human Variation
(1897)
Apparently Healthy Collection
(1717)
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(1653)
CEPH
(1611)
PIGI Consented Sample
(1356)
dbGaP
(1332)
Tourette Syndrome
(1171)
Old Order Amish Major Affective Disorder
(1009)
Repository Linkage Families
(814)
GRC
(790)
Lysosomal Storage Diseases
(786)
University of Georgia Centenarian Study
(718)
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(579)
Hybrids
(565)
GeT-RM Samples
(512)
Animals
(508)
Hereditary Cancers
(394)
Pharmacogenetics
(332)
The 90+ Study
(331)
CMD Specific
(284)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(260)
Alzheimer's Disease
(251)
Venezuelan Huntington Disease
(251)
Dystonia
(249)
Canadian Alzheimer Disease
(227)
Disorders of the Urea Cycle
(225)
Maturity-Onset Diabetes of the Young
(222)
Retinitis Pigmentosa Foundation Collection
(195)
Italian Alzheimer Disease
(122)
Nonhuman Primates
(113)
German Alzheimer Disease
(101)
FOXG1
(93)
Stem Cell Collection
(86)
Aged Sib Pairs
(73)
DGAP
(73)
Whole-Genome Sequence
(53)
Ames Dwarf Mice
(43)
Apparently healthy iPSCs
(37)
Alzheimer Disease With No Family History
(31)
Gene-Edited hiPSC
(17)
Non-Healing Wound Collection
(17)
Engineered Cell Cultures
(15)
Specially Characterized Fibroblasts
(11)
Cardiomyopathy
(6)
Frontotemporal Degeneration
(6)
Prostate Cancer
(3)
Additional PSP subjects (others grouped with Parkinsonism)
(1)
Laminopathy
(1)
Skeletal Myopathy
(1)
dbGap Data Available:
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No
(57415)
Yes
(8450)
Extended Clinical Data Available:
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Yes
(34178)
No
(31687)
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