-
V2 panel bait design test
Dataset
EGAD00001003242
-
Genomic profiling of well-differentiated and dedifferentiated liposarcoma from the same patient
Dataset
EGAD00001003976
-
Whole-genome, whole-exome and transcriptome sequencing of pancreatic ductal adenocarcinomas from young adults (NCT MASTER)
Dataset
EGAD00001004068
-
Sequencing data for oesophageal and related samples - Alex Frankell et al (RNA)
Dataset
EGAD00001004423
-
Sequencing data of primary uveal melanomas and their matched metastases
Dataset
EGAD00001004453
-
FASTQ file for paper titled "Discovery of immunotherapy targets for pediatric solid and brain tumors by exon-level expression"
Dataset
EGAD00001015356
-
The South Asia Rheumatic Heart Disease Genetics Network Data
Dataset
EGAD00001004882
-
Combination Therapies for Personalised Cancer Medicine in drug resistant EGFR mutant lung cancer (2019-06-10)
Dataset
EGAD00001005080
-
Sequencing of patient samples who received immune checkpoint inhibition - WES - NKI (2019-08-07)
Dataset
EGAD00001005235
-
Exome_Sequencing_of_Human_myeloid_malignancies (2019-08-28)
Dataset
EGAD00001005299
-
PFA ependymoma study -WGS data
Dataset
EGAD00001006045
-
WGS from PDAC samples
Dataset
EGAD00001006262
-
Single-Nuclei RNA-seq of healthy (post-mortem) and temporal lobe epilepsy (biopsy) subjects.
Dataset
EGAD00001006575
-
Whole Exome sequencing data from Shwachman-Diamond syndrome bone marrow samples
Dataset
EGAD00001006815
-
AfricanNeo WGS aDNA Dataset
Dataset
EGAD00001011320
-
Single cell TotalSeqC protein data of 20 PMBC pools of HCC patients
Dataset
EGAD00001011346
-
Sequencing Data of Leukemic Samples
Dataset
EGAD00001015662
-
eMERGE: Northwestern (NUgene) WGS
Study
phs001191
-
Copy-Number Analysis of Understudied Black Women Ovarian Cancers
Study
phs002313
-
Drug Signatures for Prediction and Mitigation of Toxicity
Study
phs002088
-
NIDDK IBD Genetics Consortium Crohn's Disease Genome-Wide Association Study
Study
phs000130
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
Download Metadata
Documentation
access/download/metadata
-
Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Study
EGAS00001005405
-
Lindsey E. Jones et al. Patient-derived cells from recurrent tumors that model the evolution of IDH-mutant glioma. Neuro-Oncology Advances, 2020. We established robust, versatile, and well-characterized Patient Derived Cells (PDC) of an IDH1-mutant astrocytoma and an IDH1-mutant oligodendroglioma that represents defined evolutionary stages of chemotherapy-induced hypermutation. The PDCs retain tumor subtype defining features over time as well as classic hallmarks of cancer, including anchorage independent growth and cell immortality. The integrated phylogenies composed of PDCs,single-cell-derived PDCs, patient-derived xenografts, and corresponding spatiotemporal tumor tissue samples also provide new insight into the clonality, evolutionary pattern, and immense mutational load of hypermutated IDH mutant gliomas.
Study
EGAS00001003992
-
A Genome-Wide Association Study in Patients Experiencing Drug-Induced Long-QT Syndrome and/or Torsades de Pointes; A Collaboration Between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Study
phs000331
-
Dissecting Cell Composition and Drug Sensitivity in Human Adenoid Cystic Carcinomas (ACCs)
Study
phs002764
-
Transcriptome study of differential expression in schizophrenia
Study
phs000775
-
Integrative Analysis for Multi-Omics Data in Non-Small-Cell Lung Cancer
Study
phs003113
-
Epstein-Barr Virus status drives morphological and molecular intra-tumour heterogeneity in gastric cancer: insights from a case report and literature review
Study
EGAS50000000706
-
Bulk RNA sequencing of day 2 and day 7 biopsies from the tuberculin skin test in people with latent tuberculosis, and of day 2 biopsies from saline controls
Dataset
EGAD50000001208
-
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
-
A comprehensive assessment of somatic mutation detection in cancer using whole genome sequencing
Study
EGAS00001001539
-
Gut metagenome associations with extensive digital health data in a volunteer-based EstMB cohort
Study
EGAS00001005900
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006233
-
Multi-omics identify falling LRRC15 as a COVID-19 severity marker and persistent pro-thrombotic signals in convalescence
Study
EGAS00001006778
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006945
-
Fetal origins of malignant germ cell tumours
Dataset
EGAD00001007037
-
An isogenic human iPSC model unravels neurodevelopmental abnormalities in SMA
Study
EGAS00001007259
-
The NCAA-DoD Concussion Assessment, Research, and Education (CARE) Consortium
Study
phs002175
-
Submitting array based metadata
Documentation
submission/metadata/submission/array
-
Genes and Blood Clotting Study (GABC)
Study
phs000304
-
Population Genetic Testing and SERPINA1 Sequencing Identifies Unidentified Alpha-1 Antitrypsin Deficiency Alleles and Gene-Environment Interaction with Hepatitis C Infection
Study
phs003297
-
Aurora US Metastatic Breast Cancer Retrospective Project
Study
phs002622
-
Brain Cell Type-Specific Enhancer-Promoter Connectivity Maps and Disease Risk Association
Study
phs001373
-
Personalized peptide vaccination among 173 patients with IDH wildtype glioblastoma: a retrospective analysis
Study
EGAS50000000449
-
INSIGHT (Intervention Nurses Start Infants Growing on Healthy Trajectories) Cohort
Study
phs001498
-
Germline Genetics of Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML)
Study
phs002962
-
Clinical Study of Intermittent Positive Pressure Breathing (IPPB-BioLINCC)
Study
phs004010
-
National Institute on Aging Genetics of Alzheimer's Disease Data Storage Site (NIAGADS)
Study
phs004180
-
Nala TAS-LRS PGx Study
Study
EGAS50000001116
-
What is metadata?
Documentation
submission/metadata/what-is-metadata
-
Exome and RNA sequencing of relapsed TCF3-PBX1 t(1;19) acute lymphoblastic leukemia
Study
EGAS00001001876
-
Comparison of 133/144bp dominant phenotype vs 166bp dominant phenotype.
Study
EGAS00001004135
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002643
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas
Study
EGAS00001002726
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_squamous_cell_carcinoma
Study
EGAS00001002725
-
Drug-perturbation-based stratification of blood cancer
Study
EGAS00001001746
-
Using_genetics_to_identify_cell_types_and_mechanisms_underlying_susceptibility_to_primary_sclerosing_cholangitis
Study
EGAS00001002642
-
Characterization_of_genomic_landscape_of_Peripheral_T_cell_Lymphomas__not_otherwise_specified__PTCL_NOS_
Study
EGAS00001002057
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__head___neck
Study
EGAS00001005450
-
Real-time analysis of the cancer genome and fragmentome from plasma and urine short and long cell-free DNA using Nanopore sequencing
Study
EGAS00001006591
-
WES data (cfTrack study) from NSCLC patients and OC patients
Dataset
EGAD00001008454
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression
Study
EGAS00000000119
-
Exome sequencing of patients with Ewings sarcoma
Dataset
EGAD00001000333
-
SNP_array
Dataset
EGAD00010001667
-
Colorectal cancer GWAS on the Spanish population
Dataset
EGAD00010001715
-
Whole-exome sequencing and microRNA profiling predicted relapse risk of stage I lung adenocarcinomas for the study and all the datasets.
Dataset
EGAD00010001902
-
methylation_bc_cervix
Dataset
EGAD00010002081
-
NSCCG_CRC_GWAS
Dataset
EGAD00010002184
-
Single-cell RNA-sequencing of peripheral blood mononuclear cells from patients with achalasia
Dataset
EGAD50000000250
-
AmsterdamUMC Data Access Committee for the study entitled "Carboxylesterase 1 mediates a distinctive metabolic profile of dendritic cells to attain an inflammatory phenotype"
Dac
EGAC50000000178
-
Korean WGS
Dataset
EGAD50000000346
-
RNA Sequencing of AD OM cells exposed to traffic-related air pollutants
Dataset
EGAD50000000648
-
Hi-C in breast healthy, primary cancer and metastatic tissues
Dataset
EGAD50000000643
-
GIST Comprehensive Cancer Panel
Dataset
EGAD50000000548
-
BAM files from capture-based targeted sequencing of 4 agressive B-cell lymphoma tumour samples (DLBCL-panel)
Dataset
EGAD50000000802
-
BIOMIROX
Dataset
EGAD50000000443
-
Expression quantitative trait loci influence DNA damage-induced apoptosis in cancer
Dataset
EGAD50000000941
-
Asan Medical Center Data Access Committee
Dac
EGAC50000000439
-
NanoSeq of buccal swab samples
Dataset
EGAD50000000999
-
WES of der(1;7)(q10;p10)
Dataset
EGAD50000000986
-
Saliva_Fulani_Database
Dataset
EGAD50000000653
-
mUM patient biopsies pre and post treatment with tebentafusp
Dataset
EGAD50000001258
-
miRNASeq profiles from Indian HFrEF Cohort
Dataset
EGAD50000001194
-
Single-cell RNA-sequencing on malignant and benign tissue samples
Dataset
EGAD50000001203
-
APS-1 TCR Sequencing
Dataset
EGAD50000000261
-
Single-Cell Profiling of the Human Endometrium in Polycystic Ovary Syndrome: Uncovering Disease Signatures and Treatment Responses
Dac
EGAC50000000468
-
Cancer Affected Patients - Data Access Committee
Dac
EGAC50000000037
-
Whone genome DNA methylation profile
Dataset
EGAD50000001815
-
Dynamic human admixture histories over the past ~1,300 years at the northern Himalayan frontier
Dataset
EGAD50000001925
-
DAC for Cornell-NCI DLBCL NGS Genomic Project
Dac
EGAC50000000704
-
Dicer and/or ADAR1 depleted HEK293-LGP2 cells
Dataset
EGAD50000002044
-
Total NF1 sequence in the patients with neurofaibromatosis type1
Study
JGAS000288
-
PacBio Revio WGS on 10 carriers of ring and marker chromosomes
Dataset
EGAD50000002111
-
RNASeq of PAX4 KO vs WT in 7 stages of differentiation from human iPSCs to BLC
Study
EGAS00001006036
-
Single cell mRNA sequencing of primary GBM - SF 10345
Dataset
EGAD00001002271
-
Sequencing of Plasma DNA from breast cancer patients
Dataset
EGAD00001006869