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Androgen deprivation therapy promotes an inflammatory and obesity-like microenvironment in periprostatic fat
Study
EGAS00001003286
-
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
Study
EGAS00001002744
-
Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer
Study
EGAS00001003791
-
Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers
Study
EGAS00001003556
-
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants
Study
EGAS00001007542
-
RNA-sequencing of tumors from 45 patients with recurrent or metastatic gastric cancer treated with immune checkpoint inhibitors
Study
EGAS00001005588
-
Exome_sequencing_of_EBV_driven_lymphoma
Study
EGAS00001001021
-
University of Utah Pelvic Organ Prolapse Disorder Study
Study
phs001439
-
A prospective study identifies MisMatch Repair genes as candidate predisposing genes for uveal melanoma.
Study
EGAS50000000914
-
Integrative analysis reveals a macrophage-predominant, immunosuppressive immune microenvironment and subtype-specific therapeutic vulnerabilities in advanced salivary gland cancer
Study
EGAS50000000809
-
Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer
Study
EGAS00001004648
-
Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): A Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study
Study
phs003066
-
Urothelial Cancer - Genomic Analysis to Improve Patient Outcomes and Research (UC-GENOME): a Bladder Cancer Advocacy Network (BCAN)-Led Collaborative Research Pilot Study - for Samples Collected at Johns Hopkins
Study
phs003094
-
Exome trios in patients with gastroschisis (2019-04-08)
Dataset
EGAD00001004942
-
Transcriptome analysis of human longitudinal whole blood samples from PCR-positive and PCR-negative adults following controlled inoculation with Influenza A (H3N2) virus.
Study
EGAS50000000679
-
STAT5 is a therapeutically targetable vulnerability in cutaneous T-cell lymphoma
Study
EGAS00001004719
-
Spatial and temporal transcriptome analysis on human skeletal muscle regeneration
Dataset
EGAD50000000263
-
Whole exome sequencing of a cold agglutinin disease patient
Study
JGAS000612
-
Whole exome sequencing of a cold agglutinin disease patient
Study
JGAS000583
-
Single-Cell Mitochondrial Variant Profiling via TAMITO-seq
Dataset
EGAD00001015494
-
Oxford Nanopore Technologies (ONT) long-read sequencing in a paired diagnostic and post- therapy medulloblastoma
Dataset
EGAD00001009490
-
Exome sequencing of a novel cervical cancer cell line
Dataset
EGAD00001004480
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Dataset
EGAD00001011260
-
A mathematical model of cell-free DNA fragment size reveals cancer-specific fragmentomic patterns
Study
EGAS50000001560
-
A comprehensive genetic map of cytokine responses in Lyme borreliosis
Study
EGAS50000000024
-
A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome
Study
EGAS00001006203
-
DLBCLR
Study
EGAS00001007479
-
Phase II Therapeutic Trial of Mexiletine in Non-Dystrophic Myotonia (IND #77,021)
Study
phs001311
-
National Cancer Institute (NCI) Genome-Wide Association Study (GWAS) of Renal Cell Carcinoma in African Americans
Study
phs000863
-
QUANTitative Chest Computed Tomography UnMasking Emphysema Progression in Alpha-1 Antitrypsin Deficiency
Study
phs000698
-
Indexing Genes Impacted by Copy Number Variation in Developmental Disorders
Study
phs001154
-
Whole genome and transcriptome sequencing of lung cancer patients and cell lines at Genentech
Study
phs000299
-
Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma
Study
phs001041
-
Genome-Wide Association Study in Systemic Sclerosis
Study
phs000357
-
Reference Standards for Mosaic Variant Detection
Study
phs003399
-
Targeted Linked-Read DNA-seq Analysis of Castration-Resistant Prostate Cancers
Study
phs003343
-
Center for Sub-Cellular Genomics
Study
phs002120
-
First datasets available in the Federated EGA Network
Blog
first-datasets-available-in-Federated-EGA
-
The circulating cell-free DNA landscape in sepsis is dominated by impaired liver clearance
Study
EGAS50000001033
-
Whole exome sequencing of an invasive diffuse intrinsic pontine glioma sampled from different sites
Study
EGAS00001002326
-
Massively parallel nanowell-based single-cell gene expression profiling
Study
EGAS00001002320
-
33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients.
Study
EGAS00001001658
-
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
-
Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
-
Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
-
Direct Comparative Analysis of 10X Genomics Chromium and Smart-seq2
Study
EGAS00001003973
-
Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
Study
EGAS50000001042
-
Genome-Wide Association Study of Celiac Disease
Study
phs000274
-
Understanding the genetic risk underlying racial disparities in uterine fibroids
Study
phs001409
-
Blood Somatic Mutations in TCGA Donors Suffering from Solid Tumors
Study
phs002867