-
Pyjacker identifies enhancer hijacking events in acute myeloid leukemia including MNX1 activation via deletion 7q
Study
EGAS50000000743
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
Autosomal Recessive PGM3 Mutations Link Glycosylation Defects to Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment
Study
phs000809
-
Rare germline variants in patients with personal and family history of colorectal cancer
Study
EGAS50000000606
-
Single-cell RNA-seq data from metastatic ovarian cancer for quality control study
Study
EGAS00001005066
-
Understanding the Progression of Metastatic Colorectal Cancer
Study
phs001722
-
DNA sequencing of sgRNAs in CRISPR-Cas9 screening and RNA sequencing of SF3B4-overexpressing liver organoids
Dataset
EGAD50000001625
-
Loss of functional mutation in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan Anemia
Study
EGAS00001000875
-
Whole genome sequencing of germline DNA from 8 patients with adult granulosa cell tumors (from blood or saliva)
Study
EGAS00001004902
-
BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - None, on genome GRCh38
Dataset
EGAD00001002395
-
BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - RPMI_BG_T=24hrs_RPMI_T=5days, on genome GRCh38
Dataset
EGAD00001002385
-
BLUEPRINT release August 2016, Bisulfite-Seq for hematopoietic multipotent progenitor cell, on genome GRCh38
Dataset
EGAD00001002434
-
BLUEPRINT release August 2014, ChIP-Seq for erythroblast
Dataset
EGAD00001000924
-
BLUEPRINT release August 2016, Bisulfite-Seq for regulatory T cell, on genome GRCh38
Dataset
EGAD00001002492
-
BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - Attached_T=1hr, on genome GRCh38
Dataset
EGAD00001002475
-
BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - RPMI_BG_T=24hrs, on genome GRCh38
Dataset
EGAD00001002441
-
BLUEPRINT release August 2016, Bisulfite-Seq for adult endothelial progenitor cell, on genome GRCh38
Dataset
EGAD00001002404
-
BLUEPRINT release August 2016, Bisulfite-Seq for Acute Promyelocytic Leukemia - CTR, on genome GRCh38
Dataset
EGAD00001002407
-
BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - RPMI_LPS_T=4hrs, on genome GRCh38
Dataset
EGAD00001002432
-
BLUEPRINT release January 2015, ChIP-Seq for erythroblast
Dataset
EGAD00001001194
-
BLUEPRINT release January 2015, ChIP-Seq for monocyte
Dataset
EGAD00001001197
-
BLUEPRINT release August 2016, Bisulfite-Seq for monocyte - RPMI_LPS_T=24hrs, on genome GRCh38
Dataset
EGAD00001002302
-
Long-term Impact and Intervention with Micronutrients in Brazil, Parque Universitário, Community-Based Study
Study
phs003175
-
Implementation of the GDPR
Documentation
about/privacy-notice
-
Primary breast cancers and paired brain metastases sequencing study
Study
EGAS00001003173
-
S3-EGA-s234-raw
Dataset
EGAD00010002624
-
S3-EGA-s234-qc1
Dataset
EGAD00010002628
-
Spatial Transcriptomic
Dataset
EGAD50000000136
-
Exome
Dataset
EGAD00001002159
-
Exome
Dataset
EGAD00001002162
-
GeneSTAR (Genetic Study of Atherosclerosis Risk) NextGen Consortium: Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
Study
phs001074
-
Genome-Wide Pleiotropy Scan Across Multiple Cancers
Study
phs002809
-
B cell receptor silencing reveals origin and dependencies of high-grade B cell lymphomas with MYC and BCL2 rearrangements
Study
EGAS50000001047
-
Synthetic data - Genome in a Bottle
Study
EGAS00001005591
-
Optimized Polyepitope Neoantigen DNA Vaccines Elicit Neoantigen-Specific Immune Responses in Preclinical Models and in Clinical Translation
Study
phs002342
-
Development of Computational Approaches for Cell Hashing in scRNA-Seq
Study
phs002695
-
Metastatic Adult Pancreatoblastoma: Multimodal Treatment and Molecular Characterization of a Very Rare Disease (NCT MASTER)
Study
EGAS00001004157
-
Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes
Study
phs002205
-
The tissue origin of highly elevated cell-free DNA in patients with and without cancer
Study
EGAS00001005400
-
Genomic Architecture of Progression and Treatment Response in AMD
Study
phs001046
-
cfMethyl-seq data (cfSort study) from serial plasma samples of NSCLC patients
Dataset
EGAD00001010881
-
Genomic Analysis of Diffuse Large B Cell Lymphoma
Study
phs003634
-
Affymetrix_Exon_Array
Dataset
EGAD00010000936
-
Illumina_1M_SNP_Array
Dataset
EGAD00010000939
-
CyclomicsSeq_Healthy_Flongle
Dataset
EGAD00001010150
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Analysis of Papilloma Infiltrating T cells from an Exceptional Responder to Immunotherapy
Study
phs002826
-
Non-coding mutations drive persistence of a founder pre-leukemic clone which initiates late relapse in T-ALL
Study
EGAS50000000129
-
Targeted_EMSeq___Development
Study
EGAS00001007202
-
Copy Number Variation in Congenital Kidney Malformations
Study
phs000565
-
Mutational landscape of renal cell carcinoma with venous tumor thrombus
Study
EGAS00001001950
-
Hi-C NTERA-2
Dataset
EGAD00010001249
-
RAGE engagement by SARS-CoV-2 enables monocyte infection and underlies COVID-19 severity
Study
EGAS00001007529
-
RFX6-mediated dysregulation defines human β cell dysfunction in early type 2 diabetes
Study
EGAS00001006273
-
TRAIP patients
Dataset
EGAD00001001633
-
CyclomicsSeq_PREDICT_R10
Dataset
EGAD00001010153
-
Sequencing of rare human histiocytic tumour
Dataset
EGAD00001002184
-
Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. WES
Study
EGAS50000000568
-
Neoadjuvant nivolumab or nivolumab plus ipilimumab in early-stage triple negative breast cancer: phase 2 adaptive BELLINI trial. RNA-Seq
Study
EGAS50000000567
-
1M-scBloodNL
Dataset
EGAD00001007764
-
Genome Sequencing Reveals That RAD50 Hypomorphism Results in Enhanced Sensitivity to Checkpoint Kinase Inhibition Combined with Chemotherapy
Study
phs000706
-
Epigenetic landscape of mixed phenotype leukemias
Study
EGAS00001007094
-
CPTAC: Proteogenomic Studies of Ovarian Tumor Responses to Agents Targeting the DNA Damage Response
Study
phs003152
-
snRNA: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000786
-
bulk ATACseq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000787
-
scATAC: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000788
-
bulk RNA-seq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000789
-
Idiopathic Collapsing Glomerulopathy in Brazilian patients
Study
EGAS50000000064
-
Identification of the cause of juvenile parkinsonism in a case_SYNJ1
Study
EGAS00001007686
-
EGAD00010000130
Dataset
EGAD00010000130
-
DNA sequencing of samples from normal tissue of colon biopsies
Dataset
EGAD00001000642
-
DNA sequencing of samples from tumoural tissue of colon biopsies
Dataset
EGAD00001000643
-
SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca2+ flux to mitochondria
Study
EGAS00001005448
-
Novel Gene-Environment Regulatory Circuit in Chamber-Specific Growth of Perinatal Heart
Study
phs002725
-
VitGene Generalized Vitiligo Genetics Study-Phase 2
Study
phs000224
-
Single-cell RNA sequencing of sorted regulatory T cells
Dataset
EGAD50000000663
-
Longitudinal Transcriptomic Profiling of Endothelial Progenitor Cells in Post-COVID-19 Patients: Insights at 3 and 6-Months Post-SARS-CoV-2 Infection
Study
EGAS50000000993
-
Chromothripsis orchestrates leukemic transformation in blast phase MPN through targetable amplification of DYRK1A
Study
EGAS00001007483
-
Discordant_Monozygotic_Twins_ALS(Genetics)
Study
EGAS50000000908
-
Detecting PKD1 variants in Polycystic Kidney Disease patients by single-molecule long-read sequencing
Study
EGAS00001002106
-
Genomic Landscape of Pediatric Myelodysplastic Syndromes
Study
EGAS00001002202
-
Emirati T2T Assembly
Study
EGAS50000001235
-
Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
-
RNA sequencing in primary inflammatory (TPP) macrophages following deletion of a disease-associated gene desert at chr21q22, disruption of ETS2, or treatment of ETS2-edited macrophages with a HIF1α stabiliser.
Study
EGAS00001007553
-
Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
-
Federated discovery and sharing of genomic data using Beacons
Blog
federated-discovery-using-beacons
-
Privacy Notice for the Account User
Documentation
data-protection/privacy-notice/ega-user-account
-
Cohort A RNA sequencing
Study
EGAS50000000950
-
SC_DDD-G-2
Dataset
EGAD00010001600
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Axiom GWAS
Study
phs001856
-
Reconstructed VDJ sequences from Smart-seq2 data
Dataset
EGAD50000000341
-
Using RNA-sequencing to characterize the resistance to lirafugratinib
Study
EGAS50000001370
-
BLUEPRINT release August 2016, ChIP-Seq for monocyte - RPMI_LPS_T=4hrs, on genome GRCh38
Dataset
EGAD00001002399
-
BLUEPRINT release August 2016, ChIP-Seq for osteoclast, on genome GRCh38
Dataset
EGAD00001002391
-
BLUEPRINT release August 2016, Bisulfite-Seq for effector memory CD8-positive, alpha-beta T cell, on genome GRCh38
Dataset
EGAD00001002383
-
BLUEPRINT release August 2016, Bisulfite-Seq for effector memory CD4-positive, alpha-beta T cell, on genome GRCh38
Dataset
EGAD00001002367
-
BLUEPRINT release August 2016, ChIP-Seq for Acute Promyelocytic Leukemia - MC2392, on genome GRCh38
Dataset
EGAD00001002406
-
BLUEPRINT September 2016, ChIPmentation Acute Myeloid Leukemia for blast cell from bone marrow, on Genome GRCh38
Dataset
EGAD00001002935
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-2)
Dataset
EGAD00001008574