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Samples (90270)
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DNA (57770)
LCL (26022)
Fibroblast (4849)
Somatic cell hybrid (320)
iPSC (316)
Plasmid (171)
mESC (103)
High Molecular Weight DNA (96)
human variation panel (69)
96 well plate of DNA samples (62)
Smooth muscle (61)
Amniotic fluid-derived cell line (60)
CEPH family kit (52)
Endothelial (47)
Adipose stromal cell (37)
Melanocyte (35)
Keratinocyte (33)
Preprocessed DNA (21)
hybrid regional mapping panel (20)
Antibodies (17)
Tumor-derived cell line (16)
Epithelial (15)
Neuronally-derived (13)
aging mapping panel (11)
Collection of iPSC (8)
Hybridoma (7)
Myeloma (7)
Protein (6)
Chorionic villus-derived cell line (4)
Mesothelial (4)
gene mutation panel (4)
hybrid mapping panel (3)
Erythroleukemic cell line (2)
Kidney-derived cell line (2)
Antigen (1)
Cytoplasmic transfer (cybrid) (1)
FFPE (1)
Microcell hybrid (1)
Peptide (1)
Virus (1)

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Whole Blood (31162)
B-Lymphocyte (26384)
LCL (22831)
Fibroblast (1678)
Skin, Arm (1074)
Skin, Unspecified (500)
Somatic cell hybrid (250)
Skin, Skin (235)
Skin, Foreskin (125)
Lung, Lung (105)
Stem cell (70)
Skin, Thigh (68)
Skin, Ear (65)
Blood (63)
Amniotic fluid (59)
Aorta, thoracic (57)
Skin, Abdomen (32)
Amniotic fluid-derived cell line (23)
Brain striatum (13)
Fetal, Unspecified (12)
Skin, Leg (12)
Skin, Posterior iliac crest (12)
Trachealis muscle (12)
Vein, iliac (11)
Gonad, Gonad (10)
Skin, Buttock (10)
Skin, Thorax (10)
Skin, Thorax/abdomen (10)
Artery, iliac (9)
Artery, pulmonary (9)
Skin, Back (9)
Umbilical Cord, Umbilical cord (9)
Skin, Buttock-thigh (8)
Skin, Inguinal area (8)
Skin, Sacrum (8)
Whole embryo, Embryo (8)
Gonad, Ovary (7)
Breast organoid (6)
Muscle, Unspecified (6)
Skin, Hip (6)
Conjunctiva, Conjunctiva (5)
Epithelial (5)
Liver, Liver (5)
Placental, Placenta (5)
Retina of eye (5)
Skin, Fetal (5)
Skin, Right ischium (5)
Chorionic villus (4)
Embryonal carcinoma (4)
Eye (4)
Gingival, Gum (4)
Gonad, Testes (4)
Chorionic villus-derived cell line (3)
Kidney, Kidney (3)
Leiomyoma (3)
Skin, Genital area (3)
Skin, Toe (3)
Smooth muscle (3)
Amnion, Amnion (2)
Aorta, abdominal (2)
Aortic arch (2)
Ascites fluid (2)
Bladder carcinoma (2)
Endometrial, Uterus (2)
Heart, Pericardium (2)
Kidney (2)
Lung (2)
Mesothelial (2)
Skin, Calf (2)
Skin, Chest (2)
Skin, Labialscrotal fold (2)
Skin, Neck (2)
Skin, Shoulder (2)
Skin, Thoraco-lumbar junction (2)
Skin, Umbilical area (2)
Spleen, Keloid (2)
T-Lymphocyte (2)
Tendon, Achilles tendon (2)
Tumor (2)
Tumor, Fibroma (2)
Tumor-derived cell line (2)
Umbilical Cord, Vein, umbilical (2)
Vein, umbilical (2)
Adenocarcinoma (1)
Adrenal cortex tumor (1)
Artery, Aorta, thoracic (1)
Artery, carotid (1)
Ascites fluid, Ascites fluid (1)
Brain, Brain (1)
Brain, Unspecified (1)
Cartilage, Nasal (1)
Cartilage, Unspecified (1)
Cervix, Cerivix uteri (1)
Chest (1)
Cornea, Cornea (1)
Endothelial (1)
Ewing sarcoma (1)
Fetal, Arm (1)
Heart, Unspecified (1)
Hydatidiform mole (1)

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NINDS Repository (54001)
NIGMS Human Genetic Cell Repository (18668)
NHGRI Sample Repository for Human Genetic Research (7509)
NIA Aging Cell Culture Repository (4438)
AREDS (2930)
AREDS2 (1988)
Autism (362)
HD Community Biorepository (207)
Allen Cell Collection (68)
NIAID - USIDnet (53)
Centers for Disease Control and Prevention Repository (27)
Orphan Disease Center (15)
CIMR Research (2)
Custom Services (1)
Human Reference Genetic Material Repository (1)

Sex:

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Female (45441)
Male (42351)
Other (26)

Race:

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White (60051)
Black/African American (7598)
More than one race (1691)
Asian (1312)
Other (1074)
Unknown (794)
Hispanic/Latino (391)
Caucasian (326)
American Indian/Alaska Native (297)
Asiatic Indian (256)
Chinese (218)
Native Hawaiian/Other Pacific Islander (103)
Not Reported (77)
East Indian (61)
Asian, Other (33)
Filipino (10)
Korean (7)
Japanese (3)
Vietnamese (3)

Affected:

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Yes (47868)
No (19085)
At Risk (6128)
Unknown (3184)

Mutation Data Available:

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N (83848)
Y (6196)
No (226)

Age at Sampling (Years):

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0-4 (3844)
5-14 (5986)
15-24 (5541)
25-34 (6770)
35-44 (9144)
45-54 (11478)
55-64 (12579)
65-74 (10926)
75-89 (6660)
90-99 (757)
100+ (244)

Collection:

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Cerebrovascular Disease (14020)
Heritable Diseases (11924)
Control (10711)
Parkinsonism (9378)
Epilepsy (7716)
NHGRI Sample Repository for Human Genetic Research (7509)
Motor Neuron Disease (5560)
Tourette Syndrome (4385)
Dystonia (4070)
Chromosome Abnormalities (2969)
Human Variation (1945)
Apparently Healthy Collection (1750)
CEPH (1671)
PIGI Consented Sample (1409)
dbGaP (1335)
Old Order Amish Major Affective Disorder (1009)
University of Georgia Centenarian Study (859)
GRC (826)
Repository Linkage Families (817)
Lysosomal Storage Diseases (803)
Muscular Dystrophies (594)
Hybrids (582)
Animals (533)
GeT-RM Samples (514)
Michigan (400)
Hereditary Cancers (398)
Massachusetts (372)
Pharmacogenetics (334)
The 90+ Study (331)
Maryland (321)
Georgia (311)
CMD Specific (290)
Illinois (277)
Pennsylvania (266)
"Intra-abdominal fat and risk of disease in children and adolescents" study (260)
Alzheimer's Disease (253)
Venezuelan Huntington Disease (251)
Disorders of the Urea Cycle (229)
Canadian Alzheimer Disease (227)
Maturity-Onset Diabetes of the Young (222)
Retinitis Pigmentosa Foundation Collection (195)
Italian Alzheimer Disease (122)
Nonhuman Primates (115)
Stem Cell Collection (103)
German Alzheimer Disease (101)
FOXG1 (93)
DGAP (74)
Aged Sib Pairs (73)
Whole-Genome Sequence (60)
Apparently healthy iPSCs (53)
Ames Dwarf Mice (47)
Alzheimer Disease With No Family History (30)
Gene-Edited hiPSC (17)
Non-Healing Wound Collection (17)
Engineered Cell Cultures (15)
Oregon (14)
Wisconsin (13)
Specially Characterized Fibroblasts (11)
Cardiomyopathy (6)
Frontotemporal Degeneration (6)
New York (3)
Prostate Cancer (3)
Johns Hopkins University (2)
Additional PSP subjects (others grouped with Parkinsonism) (1)
Laminopathy (1)
Skeletal Myopathy (1)

dbGap Data Available:

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No (74036)
Yes (16234)

Extended Clinical Data Available:

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Yes (54839)
No (35431)

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Description
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Affected
Gene
Mutations
Sex
Age at Sampling
Race
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Relationship To Proband
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Description

Product

Source

(Showing Items: 50)

View

GM21886

RING CHROMOSOME

LCL

B-Lymphocyte

View

ND41950

FOCAL DYSTONIA | CERVICAL DYSTONIA

DNA

Whole Blood

View

GM11685

CHROMOSOME 22 REGIONAL MAPPING PANEL SOMATIC CELL HYBRIDS | ADDITIONAL DELETION/DERIVATIVE CHROMOSOME 17 SOMATIC CELL HYBRIDS

Somatic cell hybrid

View

ND37943

EPILEPSY

DNA

Whole Blood

View

ND08634

ISCHEMIC STROKE

DNA

Whole Blood

View

AG20229

CENTENARIAN STUDY CENTENARIAN | GEORGIA CENTENARIAN COLLECTION - PANEL OF 100 CAUCASIAN NONAGENARIANS/CENTENARIANS

LCL

B-Lymphocyte

View

NA22596

GLAUCOMA, PRIMARY OPEN ANGLE; POAG

DNA

LCL

View

ND24870

PARKINSON DISEASE | PD

DNA

Whole Blood

View

ND42795

FOCAL DYSTONIA | CERVICAL DYSTONIA

DNA

Whole Blood

View

NA18149

CHINESE IN METROPOLITAN DENVER, COLORADO, USA

DNA

LCL

View

GM09634

NEUROFIBROMATOSIS, TYPE I; NF1

LCL

B-Lymphocyte

View

ND14408

AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1

LCL

B-Lymphocyte

View

GM11922

CEPH/UTAH PEDIGREE 1424

LCL

B-Lymphocyte

View

CD00027

HEMOGLOBIN--ALPHA LOCUS 1; HBA1 | ALPHA-THALASSEMIA (ALPHA-GLOBIN); TYPE 1 SEA HETEROZYGOTE

DNA

LCL

View

ND38616

HEREDITARY HEMORRHAGIC TELANGIECTASIA

DNA

Whole Blood

View

ND19871

PARKINSON DISEASE

DNA

LCL

View

ND44919

POPULATION/CONVENIENCE CONTROL | REGARDS STUDY COLLECTION

DNA

Whole Blood

View

GM26656

HURLER SYNDROME | ALPHA-L-IDURONIDASE; IDUA

iPSC

Fibroblast

View

ND27342

EPILEPSY

DNA

Whole Blood

View

GM19200

YORUBA IN IBADAN, NIGERIA

LCL

B-Lymphocyte

View

ND11905

POPULATION/CONVENIENCE CONTROL | CONTROL | NDPT031- AFRICAN AMERICAN CONTROL PANEL | NDPT111 - NEUROLOGICALY NORMAL AFRICAN AMERICAN CONROL PANEL

LCL

B-Lymphocyte

View

ND26515

POPULATION/CONVENIENCE CONTROL | CONTROL

DNA

Whole Blood

View

ED1229

AREDS DNA SAMPLE

DNA

LCL

View

ND01540

ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL

DNA

LCL

View

AICS-0078-079

DUAL TAGGED mEGFP-TOMM20/mTagRFPT-TUBA1B WTC iPSC LINE (BOTH MONO-ALLELIC, C-TERM/N-TERM TAGS)

iPSC

Stem cell

View

ND48075

MULTI-FOCAL DYSTONIA

DNA

Whole Blood

View

NA19564

JAPANESE IN TOKYO, JAPAN

DNA

LCL

View

ND11169

AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1 | ALS PANEL: CAUCASIANS FROM NORTH AMERICA, LOWER-LIMB ONSET | ALS PANEL; LOWER-LIMB ONSET; DEFINITE AND PROBABLE ALS

DNA

LCL

View

ND33082

TOURETTE SYNDROME

DNA

Whole Blood

View

NA11842

CEPH/UTAH PEDIGREE 1349

DNA

LCL

View

GM16220

FRIEDREICH ATAXIA 1; FRDA | FRATAXIN; FXN

LCL

B-Lymphocyte

View

ND03210

SUBARACHNOID HEMORRHAGE | SUBARACHNOID HEMORRHAGE, CAUCASIAN FROM NORTH AMERICA

LCL

B-Lymphocyte

View

ND01782

POPULATION/CONVENIENCE CONTROL | NEUROLOGICALLY NORMAL CAUCASIAN CONTROL PANEL

LCL

B-Lymphocyte

View

ND08541

ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL

LCL

B-Lymphocyte

View

ND09313

AVM-RUPTURED

LCL

B-Lymphocyte

View

NA21677

PERSONAL GENOME PROJECT | APPARENTLY HEALTHY INDIVIDUAL

DNA

LCL

View

HG01393

PUERTO RICAN IN PUERTO RICO

DNA

LCL

View

NA02525

MUCOLIPIDOSIS IV | MUCOLIPIN 1; MCOLN1

DNA

Fibroblast

View

ND25843

TOURETTE SYNDROME

DNA

Whole Blood

View

ND37024

ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL

DNA

Whole Blood

View

NA21790

MAJOR AFFECTIVE DISORDER; OLD ORDER AMISH - 125480 OR 309200

DNA

LCL

View

ND30900

HEREDITARY HEMORRHAGIC TELANGIECTASIA

DNA

Whole Blood

View

GM08400

APPARENTLY HEALTHY INDIVIDUAL

Fibroblast

View

NA16853

OSTEOGENESIS IMPERFECTA, TYPE IV; OI4 | COLLAGEN, TYPE I, ALPHA-2; COL1A2

DNA

LCL

View

ND13756

AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1

DNA

LCL

View

ND47217

SELF-REPORTED BASELINE MYOCARDIAL INFARCTION | REGARDS STUDY COLLECTION

DNA

Whole Blood

View

GM10005

TRANSLOCATED CHROMOSOME

LCL

B-Lymphocyte

View

GM09342

TUBEROUS SCLEROSIS 2; TSC2 | TSC2 GENE; TSC2

LCL

B-Lymphocyte

View

ND00249

ISCHEMIC STROKE | NDPT114 - ISCHEMIC STROKE, CAUCASIAN PANEL

DNA

LCL

View

ND10773

AMYOTROPHIC LATERAL SCLEROSIS 1; ALS1 | ALS PANEL CAUCASIAN FROM THE US

LCL

B-Lymphocyte

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