-
Ovarian carcinosarcoma genomics and eribulin response
Study
EGAS00001006555
-
Sequential single-cell transcriptional and protein marker profiling reveals TIGIT as a marker of CD19 CAR-T cell dysfunction in patients with non-Hodgkin’s lymphoma
Study
EGAS00001005356
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Dataset
EGAD00001006065
-
CSER: Clinical Implementation of Carrier Testing Using Next Generation Sequencing (NextGen)
Study
phs000927
-
Overcoming Clinical Resistance to EZH2 Inhibition Using Rational Epigenetic Combination Therapy
Study
phs003188
-
Whole Blood Transcriptomics of Patients With Melioidosis
Study
phs003724
-
A Case Controlled Etiologic Study of Sarcoidosis (ACCESS-BioLINCC)
Study
phs004276
-
Warm_autopsy__mutational_signatures_and_clonal_units
Study
EGAS00001002216
-
Exome Sequencing for Head and Neck Cancer Susceptibility
Study
phs002571
-
Whole-Genome and Exome Sequencing in clear-cell Renal Cell Carcinoma (ccRCC)
Study
phs000491
-
Single Patient BRAF Mutant Brain Tumor, Pre- and Post-dabrafenib WES.
Study
phs001629
-
Transplant Outcomes in Aplastic Anemia (TOAA): GWAS and Whole Exome Sequence Data
Study
phs001710
-
COVID_Methyl_scRNA
Dac
EGAC50000000197
-
intratumor heterogeneity in colorectal adenoma and carcinoma
Study
JGAS000092
-
Jeju Genome Project DAC
Dac
EGAC50000000938
-
Genomic and transcriptomic profiling of colorectal cancer patient-derived organoids
Study
EGAS50000001669
-
A fast, affordable and minimally-invasive diagnostic test for Cancer of Unknown Primary (CUP) using DNA methylation profiling
Study
EGAS50000000257
-
Raw and processed snRNAseq data of Choroid Plexus Tumors
Dataset
EGAD50000002320
-
PHRT longitudinal ovarian cancer dataset
Dataset
EGAD50000002064
-
PASCAL-MID Targeted amplicon sequencing of CD34+ HSPCs (CGD)
Dataset
EGAD50000001651
-
RNAseq of pre- and post-5AZA-treated head and neck cancer patients refractory to anti-PD-1 therapy
Dataset
EGAD50000001010
-
Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from the Netherlands (Ophoff)
Dataset
EGAD50000000983
-
Single cell RNA sequencing data of advanced melanoma patients treated with checkpoint inhibitor immunotherapy
Dataset
EGAD50000000493
-
RNA-seq of 2D cell culture and 3D muscle bundles generated by primary myoblast cell lines and the human iPSCs derived from mosaic FSHD patients, respectively.
Dataset
EGAD50000000717
-
STARR-seq of ERa binding sites in MCF7 and Ishikawa cell lines
Dataset
EGAD50000000015
-
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness
Study
EGAS00001001013
-
ERBB2/HER2 transmembrane and juxtamembrane domain mutations in cancer
Study
EGAS00001003213
-
Human melanoma samples with and without resistance to BRAF inhibitor therapy
Study
EGAS00001000992
-
Study of tumor RNA expression differences between treated and untreated PitNET patients
Study
EGAS00001004736
-
WGS and RNA-seq data of PC9 erlotinib-resistant and sensitive cell lines
Dataset
EGAD50000002658
-
Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Dataset
EGAD00001003409
-
Synthetic genotypes and phenotypes of 500.000 individuals
Study
EGAS00001006552
-
Molecular evolution of classic Hodgkin lymphoma revealed through whole genome sequencing of Hodgkin and Reed Sternberg cells
Study
EGAS00001006884
-
Gtag&T single-cell genome and transcriptome data
Study
EGAS00001007043
-
Molecular portraits of breast cancer diagnosed during pregnancy
Dataset
EGAD00001004353
-
Presentation and relapse myeloma
Dataset
EGAD00001004846
-
Epigenetic dysregulation in autism spectrum disorder
Dataset
EGAD00001002725
-
WGS,RNA data of patients with multiple myeloma (MM) refractory to immunomodulatory agents (IMiDs) and proteasome inhibitors (PIs)
Dataset
EGAD00001006189
-
RRBS analysis to characterize the epigenomic conservation between species in the context of Aging and Cancer.
Dataset
EGAD00001006650
-
Fine-mapping clustered GWAS hits enhances the identification of disease risk and protective genetic variants
Dataset
EGAD00001006916
-
Profiling of H3K27ac landscape in five immune cell types from rheumatoid arthritis patients and healthy controls
Dataset
EGAD00001007003
-
Reduced-representation bisulfite sequencing generated from 2 glioblastoma cell lines subjected to hypoxic and irradiation stress
Dataset
EGAD00001007770
-
RNAseq Iron-Treated iPSC-derived Microglia
Dataset
EGAD00001008660
-
Multi-region sequencing of 10 neuroblastoma cases
Dataset
EGAD00001008020
-
Single-cell RNA and TCR sequencing of BALF from 11 ICI-pneumonitis patients and 6 controls
Dataset
EGAD00001009723
-
Processed bam files for the whole exome sequencing of primary lung adenocarcinoma samples
Dataset
EGAD00001010320
-
Mtb infected and uninfected neutrophils after 1 and 6 hrs
Dataset
EGAD00001010893
-
Single cell sequencing on whole bone marrow of NBM and AML
Dataset
EGAD00001011057
-
A Genome-Wide Association Analysis in Angiotensin-Converting Enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine
Study
phs000438
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: The Genetics of Atrial Fibrillation
Study
phs002811