-
Mapping genetic variants that underlie gene regulation in intestinal cell types to identify novel, validated, Crohn’s disease drug targets
Study
EGAS00001003647
-
Acute Respiratory Distress Network (ARDSNet) Study 04 Assessment of Low Tidal Volume and Elevated End-Expiratory Volume to Obviate Lung Injury (ALVEOLI-BioLINCC)
Study
phs003714
-
Evaluation of Hybridization Capture versus Amplicon-based Methods for Whole Exome Sequencing
Study
phs000938
-
Fixed single-cell transcriptomic characterization of human radial glial diversity
Study
phs001016
-
The Research Institute at Nationwide Children's Hospital Genetics of Congenital Heart Disease (CHD)
Study
phs002010
-
Large Scale Genotyping of Psychiatric Disorders
Study
phs001413
-
Alzheimer's Disease Genetics Consortium (ADGC) Genome Wide Association Study -NIA Alzheimer's Disease Centers Cohort
Study
phs000372
-
MSK SPECTRUM - SPatiotemporal Evolution of Cancer Traced Using Multimodalities
Study
phs002857
-
The Haplotype-Resolved Genome and Epigenome of the Aneuploid HeLa Cancer Cell Line
Study
phs000642
-
Organoid BulkRNAseq
Study
EGAS50000000659
-
A Cancer Cell-Line Titration Series for Evaluating Somatic Classification
Study
EGAS00001001016
-
Towards standardized whole exome sequencing (WES) for cancer patients: lessons from a multicentric pilot study
Study
EGAS00001007363
-
Primary plasma cell leukemia (pPCL) samples were sequenced using the Nimblegen MedExome hybridization capture to detect translocations, copy number changes, and mutations in 20 pPCL samples and patient matched controls.
Study
EGAS00001003104
-
Gut 16S rRNA/FINRISK 2002
Dataset
EGAD50000000287
-
Genomic gain of EBV's LMP-1 in NKTCL
Study
EGAS50000000260
-
Profiles of extracellular miRNA in cerebrospinal fluid and serum from patients with Alzheimer's or Parkinson's disease correlate with disease status and features of pathology
Study
phs000727
-
A genome-wide CRISPR screen identifies CALCOCO2 as a regulator of beta cell function influencing type 2 diabetes risk
Dataset
EGAD50000000518
-
Immune signature of malignant melanoma in pregnancy
Study
EGAS50000000492
-
Gabriella Miller Kids First Pediatric Research Program in Bladder Exstrophy, Epispadias, Complex (BEEC)
Study
phs002173
-
A non-canonical lymphoblast in refractory childhood T-cell leukaemia
Study
EGAS50000000767
-
Single B cell analysis in pemphigus patients
Study
JGAS000281
-
Stage-specific gene and transcript dynamics in human male germ cells
Study
EGAS00001006135
-
Leucocyte eQTLs in autoimmune disease and health
Study
EGAS00001001251
-
Longitudinal analysis of treatment induced genomic alterations in gliomas
Study
EGAS00001002168
-
Personalized Onco-Genomic Project for pediatric and adolescent patients in British Columbia
Study
EGAS00001006967
-
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Dataset
EGAD00001006888
-
Single cell sequencing of a post-PD-1 inhibitor metastatic melanoma mass
Dataset
EGAD00001006013
-
WES and RNA-seq of triple-negative breast cancers from the MyBrCa cohort
Dataset
EGAD00001009311
-
Oesophageal adenocarcinoma WGS from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)
Dataset
EGAD00001009400
-
bulk RNA sequencing, single cell RNA sequencing and nanopore sequencing of T-ALL patients with TCF7-SI1 fusion
Dataset
EGAD00001007010
-
Single-cell gene expression data from CD8+ T cells from two Austrian COVID19 patients stimulated with wildtype and mutant SARS-Cov-2 peptides
Dataset
EGAD00001006995
-
Genetic landscape of inherited retinal dystrophies
Dataset
EGAD00001007022
-
Targeted myeloid panel DNA-Sequencing Mutations Matrix Validation Cohort
Dataset
EGAD00001008506
-
Paired-WGS Sequencing of Primary lymphomas of the central nervous system (PCNSL)
Dataset
EGAD00001007806
-
Adult-type Granulosa Cell Tumour of the Ovary RNA Sequencing
Dataset
EGAD00001007812
-
Neuroblastoma patient Total RNA Seq data
Dataset
EGAD00001008124
-
Distinct embryonic phylogenies and driver events of infant Wilms tumor - DNA
Dataset
EGAD00001009812
-
Dataset for other_cancer-RNA
Dataset
EGAD00001008847
-
Next Generation Children project
Dataset
EGAD00001007780
-
Somatic pathogenic variants in the normal mammary gland of sporadic breast cancer patients
Dataset
EGAD00001008327
-
Genetic landscape of SMM
Dataset
EGAD00001005285
-
Spatial and temporal intra-tumoural heterogeneity in advanced High-Grade Serous Ovarian Cancer: implications for surgical and clinical outcomes
Study
EGAS00001007164
-
Data Use Ontology (DUO)
Documentation
access/data-access-committee/data-use-ontology
-
Genomic Predictors of Combat Stress Vulnerability and Resilience
Study
phs000864
-
MP2PRT: Comprehensive Genomic Profiling to Identify Alterations Associated with Relapse for NCI Standard Risk (SR) B-Lineage ALL and NCI High Risk (HR) B-Lineage ALL with Favorable Genetic Features
Study
phs002005
-
Exome Sequencing of Esophageal Adenocarcinoma
Study
phs000598
-
Region-Specific Neural Stem Cell Lineages Revealed by Single-Cell RNA-Sequences from Human Embryonic Stem Cells
Study
phs001205
-
Multi-omics bulk and single-cell profiling of epithelioid sarcoma
Study
EGAS50000000973
-
Massively parallel nanowell-based single-cell gene expression profiling
Study
EGAS00001002320
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028