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Whole Exome Sequences of Human Embryonic Stem Cell Lines
Study
phs001343
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Genomic and Genetic Characterization of Prostate Tumors Treated with Neoadjuvant Intense Androgen Deprivation Therapy
Study
phs001938
-
Integrated Clinical and Transcriptomic Profiling to Characterize Disease Phenotype
Study
phs002121
-
NHLBI TOPMed - NHGRI CCDG: Massachusetts General Hospital (MGH) Atrial Fibrillation Study
Study
phs001062
-
Massachusetts General Hospital/Eisai National Institute of Mental Health (NIMH) Genetics Initiative Alzheimer's Disease GWAS - Affymetrix GeneChip Human Mapping 500K Array Set
Study
phs000483
-
Single Cell RNA-Sequencing in Adenoid Cystic Carcinoma
Study
phs003070
-
Genetics of Male Infertility Initiative (GEMINI)
Study
phs003115
-
Whole Exome Characterization of Squamous Cell Lung Cancers (Lung SQCC) from Appalachian Kentucky (APPKY)
Study
phs001651
-
Copy Number Variation in Congenital Kidney Malformations
Study
phs000565
-
Spatiotemporal Transcriptome of the Human Brain
Study
phs000406
-
Non Dystrophic Myotonias: Genotype-Phenotype Correlation and Longitudinal
Study
phs000578
-
Genome-Wide Environment Interaction Study on Neurodevelopment in Children from Mexico and Bangladesh
Study
phs000996
-
A Phase I/IB Study of Ipilimumab or Nivolumab in Patients With Relapsed Hematologic Malignancies After Allogeneic Hematopoietic Cell Transplantation
Study
phs002377
-
Characterization of Prostate Cancer Organoids
Study
phs001587
-
Single-cell atlas of penile cancer reveals TP53 mutations as driver for an aggressive phenotype, irrespective of HPV status, and provides clues for treatment personalization
Study
EGAS50000000217
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RNA-sequencing from duodenal bipsies of Celiac disease patients
Dataset
EGAD50000000491
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Evolutionary Pressures Shape Undifferentiated Pleomorphic Sarcoma Development and Radiotherapy Response
Study
phs003830
-
Understanding Rare Variant Contributions to autism: Lessons from Dystrofin-Deficient Model
Study
EGAS50000000754
-
Genomic analysis of head and neck squamous cell carcinoma upon acquired resistance to cetuximab
Study
EGAS50000000800
-
Targeted DNA sequencing and mRNA sequencing data from patients with peritoneal metastasis from colorectal cancer
Study
EGAS50000000404
-
Circulating cell-free DNA methylation profiles as noninvasive multiple sclerosis biomarkers: A proof-of-concept study
Study
EGAS50000001277
-
CLUSTER RNAseq Study of Juvenile Idiopathic Arthritis patients in methotrexate cohort
Study
EGAS50000000995
-
CLUSTER Read-counts matrix of RNAseq Datasets of JIA in methotrexate cohort
Study
EGAS50000001501
-
RNA seq of intestinal biopsies and blood cells from patients with celiac disease and controls
Study
EGAS50000001104
-
The EGA joins EUCAIM, the European project powering AI and imaging in cancer research
Blog
the-ega-joins-eucaim
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GCAT | Genomes for life
Blog
gcat-genomes-for-life
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Identification of point mutations, expression perturbations, and gene fusions in T-cell acute lymphoblastic leukemia by RNA-seq
Study
EGAS00001000536
-
Population whole-genome bisulfite sequencing across two tissues highlights environment as principal source of human methylome variation
Study
EGAS00001001569
-
Integrative genome profiling in AML
Dataset
EGAD00001001873
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Dataset
EGAD00001006065
-
RNA sequencing of a glioblastoma PDX cohort
Study
EGAS00001007119
-
Deciphering Intratumoral Molecular Heterogeneity in Clear Cell Renal Cell Carcinoma with a Radiogenomics Platform
Study
EGAS00001003846
-
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001004147
-
Neutrophils infected with Leishmania donovani
Study
EGAS00001004912
-
2014_Lung_sq_WES
Study
EGAS00001002844
-
Detection of Cancer Mutations by Urine Liquid Biopsy in Bladder Cancer Patients
Study
EGAS00001005758
-
Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001002438
-
'KOREAN' never-smoker female adenocarcinoma RNA-seq
Study
EGAS00001003789
-
GWAS Results from Danjou et al, Nature Genetics 2015
Study
EGAS00001003645
-
Single-cell transcriptomics identifies pathogenic T-helper 17.1 cells and pro-inflammatory monocytes in ICI-related pneumonitis
Study
EGAS00001006762
-
Methylation-based classification of human mesenchymal chondrosarcoma
Study
EGAS00001007042
-
Spatially resolved antigen receptor and gene expression data from breast cancer patients
Dataset
EGAD00001011061
-
August 2021 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001008101
-
Spatially resolved antigen receptor and gene expression data from human tonsil tissue
Dataset
EGAD00001011062
-
DAC for study Exon resequencing in patients with Brugada syndrome
Dac
EGAC00001000006
-
DAC for the "Study on the proliferation history of colorectal adenomas"
Dac
EGAC00001000209
-
DAC for study Population Structure and Genetic Diversity in Argentinean populations
Dac
EGAC00001000426
-
DAC for genome-wide association study of prognosis in Crohn's disease
Dac
EGAC00001000568
-
DAC for study Treg in breast cancer and healthy individuals
Dac
EGAC00001000638
-
DAC for NKTL study. National Cancer Centre Singapore.
Dac
EGAC00001000640