-
Whole-exome-sequencing in Charcot-Marie-Tooth disease (CMT)
Study
JGAS000337
-
CeDNN Data Access Committee UMCG
Dac
EGAC50000000584
-
Study on the Genetics of Alcoholism (COGA): African American Family GWAS
Study
phs000976
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Epilepsy: Epi25 Consortium
Study
phs001489
-
The Formation and Propagation of Human Robertsonian Chromosomes
Study
phs003920
-
Genome-Wide Association Study of the Taste and Hedonic Ratings of the Low-Calorie Sweetener Acesulfame Potassium
Study
phs004031
-
Prevention and Early Treatment of Acute Lung Injury (PETAL) Network - Functional, Imaging, and Respiratory Evaluation in CORAL (PETAL FIRE CORAL-BioLINCC)
Study
phs004130
-
Data Access Committee for Translational analyses from a phase II study of pembrolizumab and epigenetic modification with azacitidine in platinum-resistant epithelial ovarian cancer
Dac
EGAC50000000697
-
Genomic Landscape of Apical Periodontitis
Study
phs003252
-
Kids First: Whole Genome Sequencing in Structural Defects of the Neural Tube
Study
phs002591
-
Liver Regulatory Genomics Data Access Committee
Dac
EGAC50000000715
-
Cerebrospinal fluid methylome-based liquid biopsies
Study
EGAS00001006029
-
Acute Respiratory Distress Syndrome Clinical Network: Fluid and Catheter Treatment Trial (ARDSNet FACTT-BioLINCC)
Study
phs004165
-
Acute Respiratory Distress Network Early Versus Delayed Enteral Feeding to Treat People with Acute Lung Injury or Acute Respiratory Distress Syndrome (ARDSNet EDEN-BioLINCC)
Study
phs004168
-
Kids First: Whole Genome Sequencing in Recessive Structural Brain Defects
Study
phs002590
-
The Collaborative Study on the Genetics of Alcoholism (COGA)
Study
phs000763
-
Childhood Cancer Data Initiative (CCDI): Texas Pediatric Patient Derived Xenograft
Study
phs003215
-
Diabetic Retinopathy Genomics Study (DRGen) - Genetic Biomarkers of Diabetic Retinopathy
Study
phs002501
-
MP2PRT: Evaluation of an Inflammation Polygenic Risk Score (iPRS) to Predict Cancer Related Cognitive Impairment and Fatigue in Patients Receiving Chemotherapy for Non-Metastatic Breast Cancer in URCC0701 and URCC10055
Study
phs003688
-
METSIM (METabolic Syndrome In Men) Study
Study
phs000743
-
Veterans Administration (VA) Million Veteran Program (MVP) Summary Results from Omics Studies
Study
phs001672
-
Gabriella Miller Kids First Pediatric Research Program in Pediatric T-Cell Acute Lymphoblastic Leukemia
Study
phs002276
-
Genetic mutation profiling of lymphomas arising in the uterine cervix and vagina
Study
JGAS000823
-
Genetic Legacy of Punan Hunter-Gatherer Groups in Indonesian Borneo
Study
EGAS00001004471
-
Circulating cell-free DNA methylation profiles as noninvasive multiple sclerosis biomarkers: A proof-of-concept study
Study
EGAS50000001277
-
Temptation Resistance Failures: Transdiagnostic Features and Influences
Study
phs004064
-
Kids First: The Genomic Architecture of Hirschsprung Disease (HSCR)
Study
phs003662
-
NHLBI TOPMed: African American Sarcoidosis Genetics Resource
Study
phs001207
-
WES-based association study of cefaclor-induced anaphylaxis
Study
EGAS50000001163
-
Chicago Infant Mortality Study
Study
phs003790
-
Virginia PrIMeD Study
Study
phs003609
-
Identification of a Type 1 Diabetes-Associated T Cell Receptor Repertoire Signature from the Human Peripheral Blood
Study
phs003979
-
The Finland-United States Investigation of NIDDM Genetics (FUSION) Tissue Biopsy Study
Study
phs001048
-
HuBMAP: A Spatially Resolved Molecular Atlas of Human Endothelium
Study
phs002267
-
Data access to Small RNA-Seq of MicroRNA's in Tear EV's of Ushers Syndrome patients
Dac
EGAC50000000711
-
Canadian prostate cancer samples (CPC-GENE) for PanProstate study
Study
EGAS00001003037
-
German early-onset prostate cancer cohort of the Pan-Prostate Cancer Genome (PPCG) project
Study
EGAS00001003373
-
DAC for Studies of "Genetics and Genomics of Cardiovascular Diseases" Group at MDC Berlin, Germany
Dac
EGAC50000000481
-
Multiomic Landscape of Multiple Myeloma Precursor and Relapsed Disease
Study
phs003892
-
Exome Sequencing of Alcohol-Associated Hepatitis
Study
phs003659
-
Access to "BMP9 controls pulmonary vascular growth and remodeling"
Dac
EGAC50000000640
-
Whole genome sequence: cardiomyopathy, 1 HCM patient
Study
JGAS000704
-
Whole genome sequence: cardiomyopathy, 1 myotonic dystrophy patient
Study
JGAS000706
-
Whole genome sequence: cardiomyopathy, 1 ARVC patient
Study
JGAS000705
-
McGill Reproductive Genetics Data Access Committee
Dac
EGAC50000000775
-
Walter and Eliza Hall - Aix-Marseille Université
Dac
EGAC50000000655
-
genetic analysis of carcinogenesis in GAPPS
Study
JGAS000843
-
Huch Lab, Max Planck Institute of Molecular Cell Biology and Genetics
Dac
EGAC50000000112
-
APC-related multiple salivary gland lesions
Study
EGAS50000001159
-
LifeChange Data Access Committee
Dac
EGAC50000000713
-
UMCG Immunogenetics DAC
Dac
EGAC50000000785
-
ATACseq in blood-derived monocytes from CGD patients
Study
EGAS00001005915
-
Development of Novel Chondrosarcoma Organoid Models for Drug Discovery
Study
JGAS000834
-
Smoking-dependent expression alterations in nasal epithelium reveal immune impairment linked to germline variation and lung cancer risk.
Dac
EGAC50000000169
-
Idiopathic Scoliosis (SNP-array & WES study)
Study
EGAS00001008152
-
Spatial multiomic analyses reveal carcinogenic pathways in end-stage renal disease
Study
JGAS000855
-
NHLBI TOPMed: San Antonio Family Heart Study (SAFHS)
Study
phs001215
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
Genome-wide methylation profiling by high-throughput sequencing of tissue (resident) versus blood circulating memory T lymphocyte populations
Study
EGAS50000000085
-
Khoe-San genome Project (KSGP)
Dac
EGAC50000000798
-
OurHealth - Cardiovascular Disease in South Asians
Study
phs003821
-
A Case Controlled Etiologic Study of Sarcoidosis (ACCESS-BioLINCC)
Study
phs004276
-
Development of Novel Histiocytic Sarcoma Organoid Model for Drug Discovery
Study
JGAS000807
-
Development of Novel Synovial Sarcoma Organoids Models for Drug Discovery
Study
JGAS000806
-
University of Zurich (UZH) - Snedeker lab
Dac
EGAC50000000817
-
Construction of endoscopic biopsy banking for understanding the intestinal environment in colorectal diseases and exploratory studies using these banking systems.
Study
JGAS000655
-
DAC for human-derived clonal organoid studies
Dac
EGAC50000000628
-
A study on personalized medicine in genitourinary cancers using genetic biomarkers
Study
JGAS000510
-
RNA sequencing of genetically modified human iPSCs modeling patients with autism spectrum disorders (ASD)
Study
JGAS000651
-
Research for genetic causes and mechanisms of Hirschsprung's or Hirschsprung's related diseases
Study
JGAS000007
-
Phylogenetic analysis of combined lobular and ductal carcinoma of the breast
Study
JGAS000300
-
Whole genome, whole exome and transcriptome sequencing of 10 ccRCC with Von Hippel-Lindau disease
Study
JGAS000544
-
Identification of genetic mutations characteristic for recurrence and metastasis of lymphoma.
Study
JGAS000087
-
Study for establishment for effective screening and diagnosis of Lynch syndrome
Study
JGAS000638
-
New classification of occlusive cerebrovascular diseases by combining diagnostic imaging and genetic analysis of RNF213
Study
JGAS000540
-
Whole Genome Sequencing Analysis of Adult T-cell Leukemia/Lymphoma
Study
JGAS000320
-
Comprehensive genomic analysis for AYA with acute lymphoblastic leukemia
Study
JGAS000276
-
Neuron-specifc methylome analysis of Alzheimer's disease brain
Study
JGAS000125
-
Research for candidate genes of splenic epidermoid cyst
Study
JGAS000008
-
Genetic analysis in monozygotic twins discordant for bipolar disorder
Study
JGAS000014
-
Comprehansive analysis of somatic mutations and genetic variations with whole genome sequencing
Study
JGAS000516
-
Identification of genetic polymorphism on aggressive periodontitis
Study
JGAS000040
-
Identification of RNA biomarkers in Parkinson's disease patients
Study
JGAS000119
-
Target sequencing of 27 cancer-predisposing genes in Japanese colorectal cancer patients
Study
JGAS000346
-
Prevalence and Clinical Characteristics of hearing loss caused by MYH14 mutation
Study
JGAS000323
-
Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors
Study
JGAS000131
-
Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer
Study
JGAS000141
-
Identification of RNA biomarkers in Parkinson's disease iPSC-derived neuronal cells
Study
JGAS000142
-
Genetic drivers define transcriptomic characteristics and clonal hierarchy within intratumoral heterogeneity in adult T-cell leukemia-lymphoma
Study
JGAS000301
-
Whole-genome analysis of a healthy man with common trichromatic vision
Study
JGAS000348
-
Frequent post-treatment monitoring of colorectal cancer using individualized ctDNA validated by multi-regional molecular profiling
Study
JGAS000243
-
Identification of responsible genes and development of standardized medicine for familial breast cancer by genetic analysis with NGS technology
Study
JGAS000224
-
Whole-exome sequencing of pediatric solid tumors
Study
JGAS000036
-
The genetic analysis of circulating tumor DNA in blood of the digestive cancer patients to investigate the prognostic factors of metastasis and reccurence.
Study
JGAS000221
-
Whole exome sequencing of 69 trios with bipolar disorder
Study
JGAS000273
-
Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer
Study
JGAS000103
-
Elucidation of molecular mechanism of NAFLD-HCC
Study
JGAS000523
-
Somatic inflammatory gene mutations accumulate in human ulcerative colitis epithelium
Study
JGAS000199
-
Comprehensive analyses of genetic aberrations in cholangiolocarcinoma
Study
JGAS000597
-
Integrated Exome and RNA Sequencing of Dedifferentiated Liposarcoma
Study
JGAS000177