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DNA
(21013)
LCL
(10653)
Fibroblast
(1804)
iPSC
(93)
Plasmid
(64)
96 well plate of DNA samples
(34)
Preprocessed DNA
(20)
High Molecular Weight DNA
(14)
Neuronally-derived
(12)
Collection of iPSC
(8)
Amniotic fluid-derived cell line
(5)
Epithelial
(4)
Antibodies
(2)
Kidney-derived cell line
(2)
Tumor-derived cell line
(2)
aging mapping panel
(2)
Chorionic villus-derived cell line
(1)
Microcell hybrid
(1)
Smooth muscle
(1)
Source:
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Whole Blood
(11596)
B-Lymphocyte
(10665)
LCL
(8934)
Fibroblast
(564)
Skin, Arm
(273)
Skin, Unspecified
(247)
Skin, Skin
(82)
Lung, Lung
(32)
Skin, Thigh
(30)
Brain striatum
(12)
Skin, Posterior iliac crest
(9)
Amniotic fluid
(5)
Blood
(5)
Stem cell
(4)
Amniotic fluid-derived cell line
(3)
Breast organoid
(3)
Fetal, Unspecified
(3)
Kidney, Kidney
(3)
Liver, Liver
(3)
Skin, Abdomen
(3)
Skin, Buttock
(3)
Umbilical Cord, Umbilical cord
(3)
Kidney
(2)
Muscle, Unspecified
(2)
Skin, Back
(2)
Skin, Foreskin
(2)
Skin, Leg
(2)
Spleen, Keloid
(2)
Amnion, Amnion
(1)
Artery, carotid
(1)
Brain, Brain
(1)
Brain, Unspecified
(1)
Cartilage, Nasal
(1)
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(1)
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(1)
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(1)
Chorionic villus-derived cell line
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NINDS Repository
(26664)
NIGMS Human Genetic Cell Repository
(5657)
NIA Aging Cell Culture Repository
(1280)
HD Community Biorepository
(76)
Centers for Disease Control and Prevention Repository
(27)
Orphan Disease Center
(15)
Allen Cell Collection
(10)
Autism
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(299)
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(149)
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(28321)
No
(2673)
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(1552)
Unknown
(64)
Mutation Data Available:
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N
(30618)
Y
(3073)
No
(44)
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55-64
(7539)
65-74
(6309)
45-54
(6283)
75-89
(3805)
35-44
(3364)
25-34
(1796)
15-24
(1293)
5-14
(1224)
0-4
(804)
90-99
(174)
100+
(8)
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Cerebrovascular Disease
(13965)
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(6952)
Motor Neuron Disease
(5558)
Heritable Diseases
(5514)
Control
(937)
Lysosomal Storage Diseases
(653)
Apparently Healthy Collection
(438)
Muscular Dystrophies
(391)
Chromosome Abnormalities
(270)
"Intra-abdominal fat and risk of disease in children and adolescents" study
(260)
PIGI Consented Sample
(258)
Alzheimer's Disease
(251)
Venezuelan Huntington Disease
(251)
Dystonia
(250)
Old Order Amish Major Affective Disorder
(228)
Canadian Alzheimer Disease
(227)
Maturity-Onset Diabetes of the Young
(222)
Hereditary Cancers
(171)
GeT-RM Samples
(156)
CMD Specific
(150)
dbGaP
(123)
Italian Alzheimer Disease
(122)
German Alzheimer Disease
(101)
Human Variation
(54)
Animals
(33)
Alzheimer Disease With No Family History
(31)
Pharmacogenetics
(29)
Disorders of the Urea Cycle
(17)
Nonhuman Primates
(17)
CEPH
(15)
Epilepsy
(12)
Whole-Genome Sequence
(12)
DGAP
(7)
Gene-Edited hiPSC
(7)
Cardiomyopathy
(6)
Frontotemporal Degeneration
(6)
Specially Characterized Fibroblasts
(6)
GRC
(5)
Aged Sib Pairs
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Engineered Cell Cultures
(4)
Non-Healing Wound Collection
(4)
Apparently healthy iPSCs
(3)
FOXG1
(2)
Laminopathy
(1)
Skeletal Myopathy
(1)
dbGap Data Available:
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No
(28739)
Yes
(4996)
Extended Clinical Data Available:
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Yes
(26935)
No
(6800)
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