-
Spatial transcriptomics analysis of triple negative breast cancers
Dataset
EGAD50000000686
-
Contribution of systemic and somatic factors to clinical response and resistance in urothelial cancer: an exploratory multi-omic analysis
Study
phs001743
-
RNA sequencing of end-stage kidney disease patients with COVID-19
Dataset
EGAD00001009752
-
scRNAseq of aplastic anemia and healthy immune cells co-cultured with autologous HSPCs
Dataset
EGAD00001012120
-
Spatially resolved antigen receptor and gene expression data from breast cancer patients
Dataset
EGAD00001011061
-
Spatially resolved antigen receptor and gene expression data from human tonsil tissue
Dataset
EGAD00001011062
-
CRUK-ICGC Prostate Cancer Group Study
Study
EGAS00001000262
-
Psoriasis Patient PBMC scRNA-seq data
Dataset
EGAD50000001102
-
DAC-2023-07-05-Ritz (DAC-007) - Diagnosis of tuberculosis infection in children with a novel skin test and the traditional tuberculin skin test: an observational study
Study
EGAS50000000780
-
Beacon v2
Documentation
about/projects-and-funders/beacon
-
ST lobular manuscript dataset
Dataset
EGAD50000001467
-
DAC-2023-07-05-Ritz (DAC-007)
Dataset
EGAD50000001147
-
Construction of Thousands of Single Cell Genome Sequencing Libraries Using Combinatorial Indexing
Study
phs001268
-
Dataset Rdata segmentations
Dataset
EGAD00010001586
-
Human CD4+ T cells regulate peripheral immune responses in rheumatoid arthritis via IGFL2
Study
JGAS000727
-
Origins and functional consequence of somatic mitochondrial DNA mutations
Study
EGAS00001000968
-
Single-cell bam files and RNA sequencing of viral RNA stocks
Dataset
EGAD00001009711
-
Star2xml: metadata converter into XML
Documentation
tools/star2xml
-
Spatial transcriptomics analysis of triple negative breast cancers
Study
EGAS50000000475
-
PCA Atlas Visium spatial transcriptomics data (FASTQs, spaceranger BAMs and Visium mapping tables)
Dataset
EGAD00001015796
-
EGA QuickView
Documentation
access/download/visualisation/ega-quickview
-
EGA FUSE Client
Documentation
access/download/visualisation/fuse-client
-
PyEGA3 download client
Documentation
access/download/files/pyega3
-
EGA metadata schema
Documentation
submission/metadata/ega-schema
-
How to encrypt files with Crypt4gh
Documentation
submission/data/file-preparation/crypt4gh
-
Distribution of data using Live Distribution
Documentation
access/download/files/live-outbox
-
Out with the Java, in with the Python - new EGA data download client unveiled
Blog
new-ega-data-download-client
-
Programmatic submission based on XML
Documentation
submission/metadata/submission/programmatic-submission-xml
-
Papua New Guinean Genome Diversity Commitee
Dac
EGAC00001002177
-
Papua New Guinean Y chromosome Diversity Commitee
Dac
EGAC00001002531
-
Paired-end RNA-seq analysis of the TERT promoter mutant GBM cell lines
Dataset
EGAD00001005435
-
3q-capture DNA sequencing of primary AMLs with 3q26 rearrangements
Dataset
EGAD00001006820
-
Comprehensive NGS Profiling to Enable Detection of ALK Gene Rearrangements and MET Amplifications in Non-Small Cell Lung Cancer
Dataset
EGAD50000000016
-
AVENIO Expanded ctDNA panel sequence alignments (BAMs)
Dataset
EGAD50000000138
-
Access to dataset, "Feasibility of Functional Precision Medicine for Guiding Treatment of Relapsed/Refractory Pediatric Cancers"
Dac
EGAC50000000124
-
SNP Genotype Data: Subpopulations of Filipino, Malaysian, and Papua New Guinea
Study
EGAS50000000044
-
MediMer: A versatile do-it-yourself peptide-receptive MHC class I multimer platform for tumor neoantigen-specific T cell detection
Study
EGAS50000000065
-
AVENIO Expanded ctDNA panel sequence alignments (BAMs) from plasma DNA of lung cancer patients from the OSCILLATE trial
Study
EGAS50000000103
-
Sensitive circulating tumor DNA based residual disease detection in epithelial ovarian cancer
Dataset
EGAD50000000360
-
Bulk Iso-Seq from brain tissue and exosomes isolated from brain tissue using long-read PacBio sequencing of poly-adenylated transcripts
Dataset
EGAD50000000043
-
Comprehensive NGS Profiling to Enable Detection of ALK Gene Rearrangements and MET Amplifications in Non-Small Cell Lung Cancer
Study
EGAS50000000010
-
Cross-Sectional Characterization of Idiopathic Bronchiectasis
Study
phs001279
-
Discovering the Genetic Basis of Human Neuroblastoma: A Gabriella Miller Kids First Pediatric Research Program (Kids First) Project
Study
phs001436
-
International Cancer Proteogenomics Consortium (ICPC): Proteogenomics of East-Asian Breast Cancer
Study
phs003150
-
Ghana Breast Health Study
Study
phs002387
-
Joslin Study on the Genetics of Type 2 Diabetes
Study
phs002959
-
Whole Exome Sequencing and RNA-Seq to Characterize the Somatic Breast Cancer Landscape Among Latinas in California
Study
phs003218
-
NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Red Blood Cell Omics (RBC-Omics) Study
Study
phs001955
-
Genomic Predictors of Combat Stress Vulnerability and Resilience
Study
phs000864
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
Genome-Wide Association Study of HCC in Non-Asian USA Population
Study
phs001744
-
Genetic History of Neandertal and Denisovan Introgression into Melanesian Individuals
Study
phs001085
-
Drug screening of patient-derived organoids from colorectal peritoneal metastases
Study
phs002023
-
University of Pennsylvania CAR T Cell Responding and Non-responding Patients
Study
phs001707
-
Mechanism of Action of Vitamin E in NAFLD
Study
phs001930
-
Oncoarray Consortium - Lung Cancer Studies
Study
phs001273
-
National Cancer Institute (NCI) TARGET: Therapeutically Applicable Research to Generate Effective Treatments
Study
phs000218
-
Women's Health Initiative Clinical Trial and Observational Study
Study
phs000200
-
HTAN MCL Pre-Cancer Atlas Pilot Project - Targeted Sequencing Development Study
Study
phs002225
-
Treatment of Pulmonary Hypertension and Sickle Cell Disease with Sildenafil Therapy (Walk-PHaSST)
Study
phs002383
-
Strabismus, CCDD and other anomalies
Study
phs000478
-
eMERGE Network Phase III Clinical Sequencing: eMERGEseq Panel
Study
phs001616
-
Metagenomics-Guided Pathogen Discovery in Travelers' Diarrhea
Study
phs001352
-
The spectrum of somatic mutations in high-risk acute myeloid leukemia with -7/del(7q)
Study
phs000759
-
CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
-
The Genetic Landscape of Metastasis and Recurrence in Head and Neck Squamous Cell Carcinoma
Study
phs001007
-
Evaluating genetic ancestry and self-reported ethnicity in the context of carrier screening
Study
phs001482
-
National Eye Institute (NEI) Age-Related Eye Disease Study (AREDS)
Study
phs000001
-
Maintenance of Genome Sequence Integrity in Long- and Short-lived Rodent Species
Study
phs002610
-
Complete Genomics Deep Whole-Genome Sequencing of Circulating Tumor Cells from a Patient with Metastatic Breast Cancer
Study
phs001028
-
Genetic Testing to Understand and Address Renal Disease Disparities
Study
phs001620
-
A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics
Study
phs001496
-
The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Study
phs002625
-
Gabriella Miller Kids First Pediatric Research Program in Craniofacial Microsomia
Study
phs002130
-
Rare Cancer Tumors Project
Study
phs000725
-
Impact of Race and Genetic Factors on Beta Blocker Effectiveness in Heart Failure
Study
phs001501
-
Molecular Genetics of Heroin Dependence in China
Study
phs001213
-
Breast Cancer Genome Guided Therapy Study (BEAUTY)
Study
phs001050
-
National Cancer Institute (NCI) Adding Hispanics to Ongoing GWAS in Colorectal Cancer
Study
phs001193
-
Genomic Profiling of Relapsed and Refractory Childhood Cancers
Study
phs002238
-
Optimizing Primary Stroke Prevention in Children with Sickle Cell Anemia (STOP II)
Study
phs002386
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: Genetics of Coronary Heart Disease - Characterizaton of Coronary Prone Pedigrees
Study
phs001901
-
Sequencing to Guide Cancer Care (CanSeq)
Study
phs001075
-
VCRC - Giant Cell Arteritis Longitudinal Study
Study
phs000588
-
Genome-wide Association Study and Meta-Analysis of Ewing Sarcoma
Study
phs001549
-
Tumor Fraction Guided Cell-Free DNA Profiling in Metastatic Cancer Patients
Study
phs002290
-
Rare Diseases Clinical Research Network (RDCRN) Vasculitis Clinical Research Consortium (VCRC) Longitudinal Protocol for Takayasu's Arteritis
Study
phs000589
-
eMERGE: Genetics of Complex Pediatric Disorders from the Center for Applied Genomics
Study
phs001165
-
Transcriptional Profiling of Macrophages In Situ in Metastatic Melanoma Reveals Localization-Dependent Phenotypes and Function
Study
phs002564
-
National Cancer Institute Cancer Genome Characterization Initiative (CGCI)
Study
phs000235
-
GMKF: Kids First Pediatric Research Program on Congenital Cranial Dysinnervation Disorders and Related Birth Defects
Study
phs001247
-
Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS)
Study
phs000869
-
Implementation, Adoption, and Utility of Family History in Diverse Care Settings
Study
phs001641
-
Kids First Pediatric Research Study in Familial Predisposition to Hematopoietic Malignancies (SJFAMILY-HM)
Study
phs001738
-
HCI-PDX Trial Center for Breast Cancer Therapy
Study
phs002479
-
Ghana Prostate Study
Study
phs000838
-
Development and Use of Network Infrastructure for High-Throughput GWA Studies
Study
phs000234
-
University of Texas PDX Development and Trial Center Grant
Study
phs001980
-
International Standards for Cytogenomic Arrays
Study
phs000205
-
CSER: Genomic Sequencing to Aid Diagnosis in Pediatric and Prenatal Practice: Examining Clinical Utility, Ethical Implications, Payer Coverage, and Data Integration in a Diverse Population
Study
phs002324