Coriell Institute for Medical Research

Request a Quote
Donate
Login
View Cart

Samples OR Website

Search Help?

Sample Catalog | Custom Services | Core Facilities | Genomic Data Search

Biobank
Research
Services
Ordering
About Us

search submit

Clear Filter

Content Category:

apply

Samples (90243)
Website Content (2049)

Product:

apply

DNA (57751)
LCL (26023)
Fibroblast (4848)
Somatic cell hybrid (320)
iPSC (308)
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)

Source:

apply

Whole Blood (31148)
B-Lymphocyte (26385)
LCL (22832)
Fibroblast (1667)
Skin, Arm (1074)
Skin, Unspecified (500)
Somatic cell hybrid (250)
Skin, Skin (235)
Skin, Foreskin (125)
Lung, Lung (105)
Skin, Thigh (68)
Skin, Ear (65)
Blood (61)
Stem cell (61)
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)
Tumor-derived cell line (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)
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)

Repository:

apply

NINDS Repository (53989)
NIGMS Human Genetic Cell Repository (18660)
NHGRI Sample Repository for Human Genetic Research (7509)
NIA Aging Cell Culture Repository (4433)
AREDS (2930)
AREDS2 (1988)
Autism (362)
HD Community Biorepository (207)
Allen Cell Collection (66)
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:

apply

Female (45424)
Male (42345)
Other (26)

Race:

apply

White (60034)
Black/African American (7596)
More than one race (1690)
Asian (1310)
Other (1074)
Unknown (794)
Hispanic/Latino (391)
Caucasian (326)
American Indian/Alaska Native (296)
Asiatic Indian (256)
Chinese (218)
Native Hawaiian/Other Pacific Islander (103)
Not Reported (77)
East Indian (62)
Asian, Other (33)
Filipino (10)
Korean (7)
Japanese (3)
Vietnamese (3)

Affected:

apply

Yes (47850)
No (19083)
At Risk (6128)
Unknown (3183)

Mutation Data Available:

apply

N (83822)
Y (6192)
No (229)

Age at Sampling (Years):

apply

0-4 (3838)
5-14 (5985)
15-24 (5542)
25-34 (6767)
35-44 (9140)
45-54 (11476)
55-64 (12579)
65-74 (10921)
75-89 (6656)
90-99 (757)
100+ (244)

Collection:

apply

Cerebrovascular Disease (14014)
Heritable Diseases (11919)
Control (10712)
Parkinsonism (9381)
Epilepsy (7716)
NHGRI Sample Repository for Human Genetic Research (7509)
Motor Neuron Disease (5562)
Tourette Syndrome (4385)
Dystonia (4058)
Chromosome Abnormalities (2967)
Human Variation (1946)
Apparently Healthy Collection (1748)
CEPH (1671)
PIGI Consented Sample (1405)
dbGaP (1335)
Old Order Amish Major Affective Disorder (1009)
University of Georgia Centenarian Study (859)
GRC (826)
Repository Linkage Families (817)
Lysosomal Storage Diseases (800)
Muscular Dystrophies (595)
Hybrids (582)
Animals (531)
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 (252)
Venezuelan Huntington Disease (251)
Disorders of the Urea Cycle (230)
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 (51)
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:

apply

No (74017)
Yes (16226)

Extended Clinical Data Available:

apply

Yes (54800)
No (35443)

Click for fewer categories

Clear Filter

Search Results for - ~

Add Quotes

(and perform an exact match search)

Please select the fields to export

All Fields
Quick View
ID
Repository
Description
Product
Source
Affected
Gene
Mutations
Sex
Age at Sampling
Race
Ethnicity
Family
Relationship To Proband
Karyotype
Publications Cited
db Gap
Supplement
Diagnosis Age
Publications
Class
Biopsy Source
Brief Description
Chromosomal Location
Collection
Cytogenetics
Rsid
Allelic Variant 1
Construct Name
Insert Length
Vector
Concentration
Sequence
Cloning Information
Gene Bank
Mutation Description
Remarks
Hispanic Ethnicity
Country of Origin
Family Member Number
Class
Alternate IDs
Biopsy Source
Cell Type
Tissue Type
Transformant
Alias
Sample Source
Species
Common Name
Subject Type
Years Longitudinal Data
Subject Currect Age
Onset Age
External Links
PDL at Senescence
Pdl at Freeze
Passage Frozen
Supplement
Cumulative PDL at Freeze
Split Ratio
Temperature
Percent CO2
Percent O2
Medium
Serum
Substrate
Sub Cult Method
Detailed Clinical Data

← Use filters to refine search | Additional fields available - click "Fields" button

Catalog Items
Documents (2049)

Loading ...

Viewing 1 - 50 of 90243 Results

Selected Items: 0

Page Size:

Reset
Repository
Description
Product
Source
Affected
Gene
Mutations
Sex
Age at Sampling
Race
Ethnicity
Family
Relationship To Proband
Karyotype

Quick View

Description

Product

Source

(Showing Items: 50)

View

ND35085

TOURETTE SYNDROME

DNA

Whole Blood

View

ND35113

FOCAL DYSTONIA | CRANIAL DYSTONIA - UPPER AND LOWER FACIAL MOVEMENT

DNA

Whole Blood

View

ND34406

EPILEPSY

LCL

B-Lymphocyte

View

ND35125

EPILEPSY

DNA

Whole Blood

View

ND35126

ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL

DNA

Whole Blood

View

ND35141

ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL

DNA

Whole Blood

View

ND35143

POPULATION/CONVENIENCE CONTROL

DNA

Whole Blood

View

ND35140

INTRACEREBRAL HEMORRHAGE

DNA

Whole Blood

View

ND35152

TOURETTE SYNDROME

DNA

Whole Blood

View

ND35185

POPULATION/CONVENIENCE CONTROL

DNA

Whole Blood

View

ND35187

POPULATION/CONVENIENCE CONTROL

DNA

Whole Blood

View

ND35189

SUBARACHNOID HEMORRHAGE

DNA

Whole Blood

View

ND35194

PROGRESSIVE SUPRANUCLEAR PALSY

DNA

Whole Blood

View

ND35201

PARKINSON DISEASE

DNA

Whole Blood

View

ND35203

TOURETTE SYNDROME

DNA

Whole Blood

View

ND35205

TOURETTE SYNDROME

DNA

Whole Blood

View

ND35211

ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL

DNA

Whole Blood

View

ND35225

ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL

DNA

Whole Blood

View

ND35228

EPILEPSY

DNA

Whole Blood

View

ND35229

EPILEPSY

DNA

Whole Blood

View

ND35230

EPILEPSY

DNA

Whole Blood

View

NA50284

CRI-DU-CHAT SYNDROME | DERIVATIVE CHROMOSOME | COPY NUMBER VARIATION (CNV) REFERENCE PANEL 02

DNA

LCL

View

NA04678

BURKITT LYMPHOMA; BL

DNA

LCL

View

NA50115

DUPLICATED CHROMOSOME

DNA

LCL

View

HG02442

AFRICAN CARIBBEAN IN BARBADOS

DNA

LCL

View

HG02252

PERUVIAN IN LIMA, PERU

DNA

LCL

View

ND35232

TOURETTE SYNDROME

DNA

Whole Blood

View

ND35233

TOURETTE SYNDROME

DNA

Whole Blood

View

ND35250

POPULATION/CONVENIENCE CONTROL

DNA

Whole Blood

View

ND35317

SUBARACHNOID HEMORRHAGE

DNA

Whole Blood

View

ND35318

INTRACRANIAL ANEURYSM - UNRUPTURED

DNA

Whole Blood

View

ND35319

SUBARACHNOID HEMORRHAGE

DNA

Whole Blood

View

ND35332

TOURETTE SYNDROME

DNA

Whole Blood

View

ND35336

SUBARACHNOID HEMORRHAGE

DNA

Whole Blood

View

ND35337

SUBARACHNOID HEMORRHAGE

DNA

Whole Blood

View

ND35339

ASYMPTOMATIC OR UNDIAGNOSED AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL

DNA

Whole Blood

View

GM23608

ARGININEMIA

LCL

B-Lymphocyte

View

ND35353

TOURETTE SYNDROME

DNA

Whole Blood

View

ND35354

ISCHEMIC STROKE

DNA

Whole Blood

View

ND35355

INTRACEREBRAL HEMORRHAGE

DNA

Whole Blood

View

ND35357

POPULATION/CONVENIENCE CONTROL

DNA

Whole Blood

View

ND35363

SUBARACHNOID HEMORRHAGE

DNA

Whole Blood

View

ND35364

INTRACRANIAL ANEURYSM - UNRUPTURED

DNA

Whole Blood

View

ND35380

EPILEPSY

DNA

Whole Blood

View

ND35381

EPILEPSY

DNA

Whole Blood

View

GM23633

DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1A | GAP JUNCTION PROTEIN, BETA-2; GJB2 (CONNEXIN 26; CX26)

LCL

B-Lymphocyte

View

GM23654

RETT SYNDROME; RTT | METHYL-CPG-BINDING PROTEIN 2; MECP2

LCL

B-Lymphocyte

View

GM23658

ARGININOSUCCINIC ACIDURIA

LCL

B-Lymphocyte

View

GM23693

TRANSLOCATED CHROMOSOME

LCL

B-Lymphocyte

View

GM23694

TRANSLOCATED CHROMOSOME

LCL

B-Lymphocyte

No Results were Found

Show More Results

Viewing 1 - 50 of 90243 Results

Selected Items: 0

Page Size:

Repository

View Full Sample Details Add To Cart

CORIELL RESEARCH SERVICES

Apart from our online Catalog, Coriell also offers the greater scientific community a wide range of laboratory services. Our custom services include iPSC services, R&D services, assay development, custom lab services, genomic services, bioinformatic analysis, etc., to name a few.

Learn More
(Open in New Tab)

Our mission is to prevent and cure disease through biomedical research.

CUSTOMER SERVICE
customerservice@coriell.org (800) 752-3805 ● (856) 757-4848
Subscribe to our newsletter here

Coriell Institute for Medical Research
403 Haddon Avenue Camden, NJ 08103, USA (856) 966-7377

Facebook
Linkedin
Youtube

Search Results for - *~*

(and perform an exact match search)

No Results were Found

CORIELL RESEARCH SERVICES

Search Results for - ~