-
Genetic Studies in the Hutterites
Study
phs000185
-
STREP GENE: Genetics and Severe Streptococcal Infections
Study
EGAS00001003421
-
Admixture histories of São Tomé e Príncipe.
Study
EGAS50000000920
-
A distinct monocyte cellular state links systemic immune dysregulation to pulmonary impairment in long COVID
Study
EGAS50000001216
-
Spatio-temporal evolution of the primary glioblastoma genome (newly added after 2015)
Study
EGAS00001001800
-
The Genetic History of Greenlandic-European contact
Study
EGAS00001004933
-
Lothian Birth Cohort 1921 whole genome sequencing study
Study
EGAS00001003818
-
Lothian Birth Cohort 1936 whole genome sequencing study
Study
EGAS00001003819
-
Health Information National Trends Survey-SEER (HINTS-SEER)
Study
phs004065
-
Whole Transcriptome Sequencing of NXF1 or CRM1 depleted Cell
Study
JGAS000294
-
EXCEED Study
Study
EGAS00001003499
-
Landscape of Somatic Mutations in B Lymphocytes Across Human Lifespan
Study
phs001808
-
Transcriptional Profiling of PD-1+ and PD-1- Teff and Treg Cells in Glioblastoma and Health
Study
phs001079
-
An epigenetic single-cell atlas of IDH-mutant glioma reveals the role of ATRX in shaping tumor composition
Study
EGAS00001004523
-
Sequencing Study in COPD cases and controls
Study
EGAS00001003406
-
Prediction of plasma ctDNA fraction and prognostic implications of liquid biopsy in advanced prostate cancer
Dataset
EGAD50000000303
-
Genetic Determinants of Viral Clearance in HCV-Infected Populations
Study
phs000248
-
Identification of hypermutation and defective mismatch repair in ctDNA from metastatic prostate cancer
Study
EGAS00001003899
-
TOTHER3 dataset
Dataset
EGAD50000000562
-
HIV-phyloTSI: Subtype-independent estimation of time since HIV-1 infection for cross-sectional measures of population incidence using deep sequence data
Study
EGAS50000000895
-
Collaborative Cohort of Cohorts for COVID-19 Research (C4R): Severe Asthma Research Program (SARP)
Study
phs002913
-
BIRC5 Upregulation Enhances DNMT3A-Mutant T-ALL Cell Survival and Pathogenesis
Study
phs003623
-
Genetic mutation profiling of lymphomas arising in the uterine cervix and vagina
Study
JGAS000823
-
RNAseq of primary mesothelioma cell lines
Dataset
EGAD00001010924
-
RNAseq of primary mesothelioma cell lines
Dataset
EGAD00001009642
-
Epigenomics Studies in Acute Myeloid Leukemia (AML)
Study
phs001027
-
HiDEF-seq single-molecule sequencing of single-strand mismatches and damage
Study
EGAS50000000318
-
Genomics of Acute Myeloid Leukemia
Study
phs000159
-
Genomic landscape of Ewing sarcoma (ICGC project)
Study
EGAS00001000855
-
WGS of primary mesothelioma cell lines
Dataset
EGAD00001009641
-
Clinical relevance of TCGA subtypes for gastric cancer patients
Study
EGAS50000000779
-
The Oral Microbiome and Head and Neck Cancer
Study
phs004018
-
3.5KJPNv2, an allele frequency panel of 3,552 Japanese individuals
Study
JGAS000159
-
FOXM1 is a biomarker of resistance to PI3Kα inhibition in ER+ breast cancer that is detectable using metabolic imaging (RNA-seq data)
Study
EGAS00001004452
-
Hereditary Cancer Diagnostics with I2HCP gene panel
Dataset
EGAD00001006171
-
Foundation Medicine Adult Cancer Clinical Dataset (FM-AD)
Study
phs001179
-
Study of Adaptation to Hypoxia in Ethiopian Highlanders via Whole Genome Sequencing
Study
phs000647
-
Genome-Wide Analysis of Splenic Marginal Zone Lymphoma
Study
phs000502
-
The Prostate, Lung, Colon, Ovary Screening Trial (PLCO)
Study
phs001286
-
Single Cell DNA Methylation Analysis for Forensic Epigenetics
Study
phs003204
-
Transcriptome of human trophoblast stem cells derived from normal and HDP placentas
Study
JGAS000660
-
European Genome-phenome Archive 15th Anniversary Celebration
Blog
15-anniversary
-
The Simons Genome Diversity Project: 300 genomes from 142 diverse populations
Study
EGAS00001001959
-
Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
-
H3Africa Chip Design - Aim of designing a cost-effective GWAS chip with content appropriate for use in genomics studies of individuals from the African continent.
Study
EGAS00001002976
-
RNA stability controlled by m6A methylation contributes to X-to-autosome dosage compensation in mammals
Study
EGAS00001007112
-
LLDeep DAG2+ scRNA-seq in PBMCs
Dataset
EGAD00010001315
-
Neonatal and adult recent thymic emigrants produce IL-8 and express complement receptors CR1 and CR2
Dataset
EGAD00001003793
-
SCANDARE HNSCC DNA targeted panel sequencing
Dataset
EGAD50000001654
-
LLDeep DAG2+: scRNA-seq in PBMCs
Dataset
EGAD00001003459
-
Integrating Genomic and Transcriptomic Data to Identify Breast Cancer Susceptibility Genes
Study
phs003535
-
Mitochondrial Abnormalities in Schizophrenia and Bipolar Disorder
Study
phs002395
-
Vanderbilt Genome-Electronic Records (VGER) Project: QRS Duration
Study
phs000188
-
California Teachers Study (CTS): Whole Genome Sequences From Under-Represented Populations
Study
phs002918
-
1000 Genomes Used for Cloud Testing
Study
phs000710
-
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
-
A microRNA-signature that correlates with cognition and is a target against cognitive decline
Study
EGAS00001005627
-
Mapping the human hematopoietic stem and progenitor cell hierarchy through integrated single-cell proteomics and transcriptomics
Study
EGAS00001007930
-
Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Study
EGAS00001005736
-
HiDEF-seq single-molecule sequencing of single-strand mismatches and damage
Dataset
EGAD50000000460
-
SCANDARE HNSCC 3' Tag RNA-seq
Dataset
EGAD50000001655
-
SCANDARE TNBC WES data
Dataset
EGAD50000001661
-
SCANDARE TNBC WGS data
Dataset
EGAD50000001662
-
SCANDARE TNBC shallow WGS data
Dataset
EGAD50000001849
-
SCANDARE ovarian WES data
Dataset
EGAD50000001658
-
SCANDARE TNBC transcriptomics data
Dataset
EGAD50000001416
-
Whole Exome Sequencing of Pancreatic Neuroendocrine Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Study
phs000871
-
HiDEF-seq Single-Molecule Sequencing of Single-Strand Mismatches and Damage
Study
phs003604
-
Acute Respiratory Distress Network (ARDSNet) Study 02 Late Steroid Rescue Study (LaSRS) (ARDSNet-LaSRS-BioLINCC)
Study
phs003769
-
Synthetic - FEGA Sweden Heilsa synthetic dataset December 2023
Study
EGAS50000000086
-
Single cell RNA seq of breast cancer stem cells
Study
JGAS000305
-
Sequencing_Acute_Myeloid_Leukaemia_
Study
EGAS00001000035
-
Genetic_mechanisms_of_resistance_to_chemotherapy_in_breast_cancer
Study
EGAS00001000276
-
DNA methylation atlas of normal human cell types
Study
EGAS00001006791
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Study
EGAS00001004364
-
Interferon lambda 4 impairs viral antigen presentation and attenuates T cell responses
Study
EGAS00001005396
-
BAMSE (Swedish abbreviation for Children, Allergy, Milieu, Stockholm, Epidemiology)
Study
EGAS00001002746
-
SNP array files, IDAT files, from 34 members of a Family with a high prevalence of psychosis
Study
EGAS00001004592
-
RNA stability controlled by m6A methylation contributes to X-to-autosome dosage compensation in mamals
Dataset
EGAD00001010194
-
Early Family Prevention of Adolescent Alcohol, Drug Use, and Psychopathology
Study
phs003442
-
Blood Group Genotypes and Phenotypes in Omani Blood Donors and Its Links With Susceptibility to Malaria
Study
phs003694
-
Widespread DNA hypomethylation and differential gene expression in Turner syndrome
Study
EGAS00001002190
-
Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region mutation and known pathogenic mutation in SPG11
Study
EGAS00001001849
-
Biased allelic expression in human primary fibroblast single cells.
Study
EGAS00001001009
-
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Study
EGAS00001002903
-
Next Generation Sequencing in an IBD Pedigree Whole Genome Data
Dataset
EGAD00001000399
-
Human Microbiome Project Demonstration Study of Cutaneous Microbiome in Psoriasis
Study
phs000251
-
Relationship between low LDL cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: a US-based cross-sectional observational study using electronic medical records
Study
phs001588
-
Sporadic Amyotrophic Lateral Sclerosis (ALS): Parent-Offspring and Twin Sequencing Study
Study
phs000831
-
Cardiovascular Health Study (CHS) - Imaging
Study
phs003639
-
Hematopoietic Tet2 inactivation enhances the response to checkpoint blockade immunotherapy
Study
EGAS50000001191
-
Drug Development against Tumor Microtube Networks in Glioblastoma
Study
EGAS50000000477
-
Exploring the role of mtDNA variation in Multiple Sclerosis in a large cohort of discordant monozygotic twins
Study
EGAS00001001240
-
Cardiovascular disease biomarkers derived from circulating cell-free DNA methylation
Study
EGAS00001007263
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005214
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005215
-
Synthetic - FEGA Sweden Heilsa synthetic dataset December 2023
Dataset
EGAD50000000119
-
High Density SNP Association Analysis of Lung Cancer
Study
phs000753
-
Fixed single-cell transcriptomic characterization of human radial glial diversity
Study
phs001016
-
AIDS Linked to the Intravenous Experience (ALIVE) Cohort
Study
phs001494