-
Epidemiological study comparing rates and risk factors for dementia in African Americans in Indianapolis and Yoruba living in Ibadan, Nigeria
Study
phs000378
-
Prevention and Early Treatment of Acute Lung Injury (PETAL) Crystalloid Liberal or Vasopressors Early Resuscitation in Sepsis (CLOVERS) (PETAL CLOVERS-BioLINCC)
Study
phs004080
-
Cloning of the breakpoint of a novel translocation associated with T-acute lymphoblastic leukaemia
Dataset
EGAD00001002193
-
Poly(A) RNA sequencing of hepatocellular carcinoma tumors and their matched noncancerous liver tissues
Study
EGAS00001002337
-
A unidirectional histone code in bidirectional promoters across cell types
Study
EGAS00001001656
-
WNT-dependent interaction between inflammatory fibroblasts and FOLR2+ macrophages promotes fibrosis in chronic kidney disease
Study
EGAS50000000101
-
Genetic Basis of Breast Cancer Resistance in BRCA1 Mutation Carrier
Study
phs001243
-
VA APOLLO Project - Research for Precision Oncology (RePOP)
Study
phs001374
-
CIDR Whole Exome Sequencing in Joubert Syndrome
Study
phs000382
-
Integrated Analysis of Multimodal Single-Cell Data
Study
phs002315
-
Genomics of Circulating Tumor Cells
Study
phs000717
-
Detecting and Subtyping Lung Cancer Through Analysis of Circulating Tumor DNA
Study
phs003570
-
Distinct immune cell infiltration patterns in PDAC exhibit divergent immune cell selection and immunosuppressive mechanisms
Study
EGAS50000000726
-
The genomic basis of childhood T-lineage acute lymphoblastic leukemia
Study
EGAS50000000016
-
CSER: Exome Sequencing in Diverse Populations in Colorado and Oregon/CHARM Cancer Health Assessments Reaching Many
Study
phs002111
-
M116 Proteome Extracellular Vesicle Profiling
Dataset
EGAD50000001679
-
Induction of fetal meiotic oocytes from embryonic stem cells in cynomolgus monkeys
Study
JGAS000573
-
Increased mutation accumulation during fetal development in Down syndrome
Study
EGAS00001003982
-
Study on the proliferation history of colorectal adenomas
Study
EGAS00001000883
-
Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors
Study
EGAS00001003530
-
Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T-cell lymphomas with hemophagocytic lymphohistiocytic syndrome
Study
EGAS00001002765
-
SINGLE_CELL_ANALYSIS_OF_IN_VITRO_ERYTHROPOIESIS
Study
EGAS00001000764
-
Cryptic Relatedness in the Singapore Living Biobank Project
Study
EGAS00001002619
-
Defective T-cell expansion in RASGRP1 deficiency
Study
EGAS00001002753
-
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
-
Genome Diversity in Africa Project: Benin (2021-02-16)
Dataset
EGAD00001006970
-
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
-
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
-
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
-
Exome trios in patients with gastroschisis (2019-04-08)
Dataset
EGAD00001004942
-
Evaluating potential drug candidates for the treament of Henamgiopericytoma on patient derived cell line models
Study
EGAS50000000027
-
RNAseq and ATACseq on HGSC lines, pre- and post-treatment with an epigenetic drug
Study
EGAS50000000047
-
Comprehensive NGS Profiling to Enable Detection of ALK Gene Rearrangements and MET Amplifications in Non-Small Cell Lung Cancer
Study
EGAS50000000010
-
Exome Sequencing of Chordoma Cases
Study
phs001280
-
Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer
Study
phs001940
-
Epigenetic Moderators of Naltrexone Efficacy for Alcohol Use Disorder
Study
phs002424
-
Family-Based Study on Ulcerative Colitis with Whole Exome Sequencing
Study
phs001251
-
Exome Sequencing of Pleuropulmonary Blastoma
Study
phs000543
-
Diagnostic yield and clinical utility of whole-exome sequencing in pediatric patients with rare and undiagnosed diseases in the Czech Republic
Study
EGAS50000000442
-
LungMAP: Molecular Atlas of Lung Development - Human Lung Tissue
Study
phs001961
-
Single-cell RNA-seq profiling of patient derived organoids
Study
EGAS50000001025
-
single nuclei multiomics (ATAC-RNA) of KOLF2.1J human induced pluripotent stem cells-derived differentiated dopaminergic neurons
Study
EGAS50000001418
-
RNA sequencing of genetically modified human iPSCs modeling patients with autism spectrum disorders (ASD)
Study
JGAS000651
-
Genomic evolution of pancreatic cancer at single-cell resolution
Study
EGAS50000001351
-
CAGEKID: Cancer Genomics of the Kidney
Study
EGAS00001000083
-
Ribosome_Profiling_of_Macrophages_during_Salmonella_Infection
Study
EGAS00001001285
-
The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples
Study
EGAS00001005055
-
Mutant_clone_mapping_in_normal_oesohagus_and_skin_2
Study
EGAS00001005659
-
COVID-19 Severity of First Wave of Infection for Severe Patients in Madrid
Study
EGAS00001005931
-
Finding structural variation from the human skin fibroblast at the single-cell level
Study
EGAS00001006498
-
Multiomics analyses of Parkinson's disease midbrains
Study
EGAS00001004966
-
Exome sequencing of matching primary tumor and venous tumor thrombus (VTT) renal cell carcinoma (RCC) samples
Dataset
EGAD00001004887
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - WGS
Dataset
EGAD00001011645
-
Whole Transcriptome Analysis + AbSeq + Sample Tag Multiplexing
Dataset
EGAD00001011318
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - scRNA
Dataset
EGAD00001011647
-
An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - RNA
Dataset
EGAD00001011646
-
CAGEKID: Cancer Genomics of the Kidney - Targeted Sequencing
Study
EGAS00001007004
-
PhIP-Seq data
Study
EGAS00001007054
-
cfDNA exercise - methylation array
Dataset
EGAD00010002497
-
USH genes sequencing
Study
EGAS50000000476
-
Sharma/Busskamp Retinal Organoid
Dac
EGAC50000000487
-
Kidney_tumour_RNA
Study
EGAS00001002487
-
WGS data from a GBM patient PT-HS9105
Dataset
EGAD00001004244
-
A Multiethnic Genome-wide Scan of Prostate Cancer
Study
phs000306
-
University of Utah Pelvic Organ Prolapse Disorder Study
Study
phs001439
-
Medulloblastoma dataset
Dataset
EGAD50000000384
-
Whole_Exome_Sequencing_of_INTERVAL
Study
EGAS00001000825
-
Paediatric IBD Mosaicism
Study
EGAS00001002489
-
Genentech - Cell line exome sequencing
Study
EGAS00001002554
-
Multi-region WGS of a RET fusion positive cancer
Dataset
EGAD00001006878
-
Integrative analysis reveals a macrophage-predominant, immunosuppressive immune microenvironment and subtype-specific therapeutic vulnerabilities in advanced salivary gland cancer
Study
EGAS50000000809
-
A prospective study identifies MisMatch Repair genes as candidate predisposing genes for uveal melanoma.
Study
EGAS50000000914
-
Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer
Study
EGAS00001004648
-
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
-
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
-
First datasets available in the Federated EGA Network
Blog
first-datasets-available-in-Federated-EGA
-
Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
Study
EGAS50000001042
-
A model for predicting response to PD-1 inhibitors in NSCLC
Study
phs002244
-
Heterogeneity and evolution of DNA mutation rates in microsatellite-stable colorectal cancer
Dataset
EGAD50000000616