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Genomic Characterization CS-MATCH-0007 Arm U
Study
phs002179
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Genomic Characterization CS-MATCH-0007 Arm C1
Study
phs002177
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Genomic Characterization CS-MATCH-0007 Arm P
Study
phs002152
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The Contribution of De Novo Coding Mutations to Meningomyelocele
Study
phs003746
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The Genetic Evolution of Acral Melanoma
Study
phs003451
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Immune Determinants of Resistance to PD-1 Blockade in Renal Cell Carcinoma
Study
phs003618
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Longitudinal Study of Vaginal Flora
Study
phs002367
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The Prostate, Lung, Colon, Ovary Screening Trial (PLCO)
Study
phs001286
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Genomic Characterization CS-MATCH-0007 Arm Q
Study
phs001926
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Beacon v2 and Federated EGA, part of the GDI project Starter Kit to enable access to genomic and phenotypic data across borders
Blog
beacon-v2-and-federated-ega-part-of-the-gdi-project-starter-kit
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Human papillomavirus integration induces oncogenic host gene fusions in oropharyngeal cancers
Study
EGAS50000000892
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TenK10K Phase 1: Single Cell
Study
EGAS50000001653
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Genomic profile of sporadic multiple meningiomas
Study
EGAS00001005700
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RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
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English Longitudinal Study of Ageing Genome-wide genotyping using the Illumina HumanOmni2.5-8
Study
EGAS00001001036
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Exome Sequencing in Moebius Syndrome
Study
EGAS00001001250
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Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids
Study
EGAS00001000650
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Genome-wide DNA methylation profiles by MeDIP-seq of cord blood cells and cord blood mononuclear cells obtained from twins conceived through in vitro fertilization and naturally conceived controls
Study
EGAS00001002248
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Single cell RNAseq of PBMC from bladder cancer patients
Study
EGAS00001004008
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Single cell RNAseq of PBMC from RCC patients
Study
EGAS00001004451
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Single-cell analysis reveals fibroblast clusters linked to immunotherapy resistance in cancer
Study
EGAS00001004030
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Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Study
EGAS00001003367
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Multi-omic Profiling of Central Nervous System Leukemia Identifies mRNA Translation as a Therapeutic Target
Study
EGAS00001005647
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Organoid drug profiling identifies methotrexate as a therapy for SCCOHT, a rare pediatric cancer
Study
EGAS00001007911
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Mechanisms of Therapy Driven Clonal Evolution in Oncogenic RAS Mutant Relapsed Acute Lymphoblastic Leukemia
Study
phs001072
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Primary Prostate Tumor Tissue DNA Methylation Profiles
Study
phs001921
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Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)
Study
phs000652
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Genome-Wide Discovery of Novel Breast Cancer Predisposing Mutations
Study
phs000822
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Kids First: Whole Genome Sequencing of Nonsyndromic Craniosynostosis
Study
phs001806
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Clinical Resistance to Crenolanib in Acute Myeloid Leukemia Due to Diverse Molecular Mechanisms
Study
phs001628
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VA APOLLO Project - Research for Precision Oncology (RePOP)
Study
phs001374
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Pharmacogenomic Interactions in Glioblastoma Cell Line Models
Study
phs001793
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Human Blastocyst 10X Single Cell RNA Sequencing
Study
phs003122
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Somatic Mutations in Single Human Neurons from Patients with Congenital Neurodegenerative Diseases
Study
phs003005
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Kids First: The Genomic Architecture of Hirschsprung Disease (HSCR)
Study
phs003662
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Response to tumor-infiltrating lymphocyte adoptive therapy is associated with preexisting CD8+ T-myeloid cell networks in melanoma
Study
EGAS50000001217
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Identification of HER2-positive breast cancer molecular subtypes with potential clinical implications in the ALTTO clinical trial
Study
EGAS50000000525
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Genome‐wide postnatal changes in immunity following fetal inflammatory response
Study
EGAS00001003635
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RNA-sequencing of tumors from 45 patients with recurrent or metastatic gastric cancer treated with immune checkpoint inhibitors
Study
EGAS00001005588
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Whole Mitochondrial Sequencing of Gingivo-buccal Cancer: ICGC-India Project
Study
EGAS00001002425
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The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
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UAMS Smoldering Myeloma Myeloma Sequencing
Study
EGAS00001003629
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Identification of rare germline variants in familial multiple myeloma
Study
EGAS00001004734
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Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Study
EGAS00001004267
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Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation.
Study
EGAS00001005874
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Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer
Study
EGAS00001006200
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MGP Panel: a comprehensive targeted genomics panel for molecular profiling of multiple myeloma patients
Study
EGAS00001006222
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An Atlas of Cells in the Human Tonsil
Study
EGAS00001006375
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Covid19 Transcriptomic Data analysis in Irish Population
Study
EGAS00001007116
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Whole genome sequencing analysis of hepatoblastoma
Study
JGAS000156
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Duplex Sequencing of normal and tumor tissues from case 2 and case 3 (10 DS)
Dataset
EGAD50000000239
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The biology of cell-free DNA fragmentation and the roles of DNASE1, DNASE1L3 and DFFB
Dataset
EGAD00001005371
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Genomics_of_Colorectal_Cancer_Metastases___Massively_Parallel_Sequencing_of_Matched_Primary_and_Metastatic_tumours_to_Identify_a_Metastatic_Signature_of_Somatic_Mutations__MOSAIC_
Study
EGAS00001000103
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Organoid_Derivation_Project__TGS
Study
EGAS00001002221
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FWO_project_G_0687_12_X10_WGS
Study
EGAS00001001145
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Whole exome sequencing of PMBCL
Study
EGAS00001006235
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Characterizing the Role of the Immune Microenvironment in Multiple Myeloma Progression at a Single Cell Level
Study
phs002756
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The Pioneer 100 Wellness Project (P100)
Study
phs001363
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NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Lung Health Study of Chronic Obstructive Pulmonary Disease)
Study
phs000291
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Genetics of 24 hour urine composition
Study
phs000460
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Michigan Polybrominated Biphenyl (PBB) Exposure Registry
Study
phs001862
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Biomarkers in Transplant Recipients
Study
phs000960
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Region-Specific Neural Stem Cell Lineages Revealed by Single-Cell RNA-Sequences from Human Embryonic Stem Cells
Study
phs001205
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Center for Sub-Cellular Genomics
Study
phs002120
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Comprehensive Genomic Characterization of Translocation Renal Cell Carcinoma
Study
phs003008
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Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
Study
EGAS50000001042
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UK10K_RARE_HYPERCHOL
Study
EGAS00001000129
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Identification_of_synthetic_lethal_genes_by_CRISPR_Cas9_library
Study
EGAS00001002117
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Initial whole genome sequencing of plasma cell neoplasms in First Responders exposed to the World Trade Center attack of September 11, 2001
Study
EGAS00001004467
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Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth
Study
EGAS00001007555
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NHLBI GO-ESP: Early-Onset Myocardial Infarction (Broad EOMI)
Study
phs000279
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Identification of Somatic Changes in Tumors from Fanconi Anemia Patients
Study
phs002652
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Contextual and Health Behavior Effects on Epigenetic Aging Among Africans in the Family and Community Health Studies
Study
phs003723
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Security Overview
Documentation
about/security
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UK10K NEURO IOP COLLIER
Study
EGAS00001000121
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Neoantigen-Targeted CD8+ T-Cell Responses 1 With PD-1 Blockade Therapy
Study
phs003153
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Genomic Diagnosis and Individualized Therapy of Highly Penetrant Genetic Diabetes
Study
phs001771
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Study of Melanoma Risk in Australia and the United Kingdom
Study
phs000519
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North American Mitochondrial Disease Consortium Patient Registry and Biorepository
Study
phs001538
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Rapid Acceleration of Diagnostics - Underserved Populations (RADx-UP): CO-CREATE-Ex: Community-engaged Optimization of COVID-19 Rapid Evaluation And TEsting Experiences
Study
phs003686
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Women's Environmental Cancer and Radiation Epidemiology (WECARE) Study
Study
phs003945
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CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
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Light at Night and Prostate Cancer in the Health Professionals Follow-Up Study
Study
phs003538
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WGS, DuplexSeq and NanoSeq genomic data from histologically normal tissue in cancer patients
Study
EGAS00001008326
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The G2 gene expression signature and MYC overexpression are independent poor prognostic factors in childhood high-grade osteosarcoma
Study
EGAS00001008073
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Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis
Study
phs000239
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Nasal MicroRNA during Bronchiolitis and Age 6y Asthma: MARC-35 Cohort
Study
phs003564
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Mayo Clinic - Fecal Microbiota and Adenomas
Study
phs001204
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Case Report: Pre-Clinical Combination Targeting VEGF and PI3K in a Rare, Aggressive Mixed Endometrial Carcinoma
Study
EGAS50000001665
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DNA methylation and the adverse metabolic outcomes of adiposity
Study
EGAS00001001922
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Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058
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Benchmarking for alignment and variant calling
Study
EGAS00001007819
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Epidemiological study comparing rates and risk factors for dementia in African Americans in Indianapolis and Yoruba living in Ibadan, Nigeria
Study
phs000378
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Broccoli Sprouts Extracts Trial (BEST-COPD-BioLINCC)
Study
phs004022
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Sporadic Amyotrophic Lateral Sclerosis (ALS): Parent-Offspring and Twin Sequencing Study
Study
phs000831
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Epigenetic Changes in Immune Response and Oncogenesis Related Genes Caused by Heavy Metal Long-Term Exposure
Study
phs003392
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Precision Medicine for Dilated Cardiomyopathy in European and African Ancestry
Study
phs002641
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Gene Expression and Biomarker Utility in Post-Mortem Samples
Study
phs003546
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Gynecology and Lubricant Effects (GALE) Study
Study
phs002211
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Single-Cell Genomic and Transcriptomic Analysis of the Aging Human Brain
Study
phs003445