-
The Dynamic Landscape of Open Chromatin During Human Cortical Neurogenesis
Study
phs001438
-
Estrogen Receptor Positive Breast Cancer: Aromatase Inhibitor Response Study
Study
phs000472
-
National Heart, Lung, and Blood Institute (NHLBI) Heart Healthy Lenoir (HHL) Genomics Study
Study
phs001471
-
Adoptive Cell Therapy of Autologous T cell Receptor-Engineered T Cells Targeting the p53 Neoantigens in Human Solid Tumors
Study
phs002928
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Italian Atherosclerosis Thrombosis and Vascular Biology
Study
phs000814
-
Consanguinity and rare mutations outside of MCCC genes underlie non-specific phenotypes of MCC Deficiency
Study
phs000776
-
The Immune Microenvironment Shapes Transcriptional and Genetic Heterogeneity in Chronic Lymphocytic Leukemia
Study
phs002297
-
Adolescent Idiopathic Scoliosis (AIS) 1000 Exomes Study
Study
phs001677
-
NHLBI TOPMed: Whole Genome Sequencing of Venous Thromboembolism (WGS of VTE)
Study
phs001402
-
The Mutational Landscape of CTCL and Sezary Syndrome
Study
phs000994
-
Analysis of Epigenomes and Genome Topology in Colorectal Cancer
Study
phs002288
-
Gabriella Miller Kids First Pediatric Research Project in Cornelia de Lange Syndrome, Related Diagnosis and Structural Birth Defects
Study
phs002174
-
Normal Pressure Hydrocephalus
Study
phs002296
-
Acute Respiratory Distress Network (ARDSNet) Study 02 Late Steroid Rescue Study (LaSRS) (ARDSNet-LaSRS-BioLINCC)
Study
phs003769
-
Anti-myeloperoxidase IgM B cells in anti-neutrophil cytoplasmic antibody-associated vasculitis
Study
EGAS50000000753
-
Gene expression adaptation of metastases to their host tissue
Study
EGAS50000000817
-
Characterization of High-Grade Serous Ovarian Cancer Subtypes via Single-Cell and Spatial-Transcriptomics Profiling
Study
phs002262
-
Genome-wide analyses of cell-free DNA for therapeutic monitoring of patients with pancreatic cancer
Study
EGAS50000000923
-
Response to Tagraxofusp in Blastic Plasmacytoid Dendritic Cell Neoplasm
Study
phs003895
-
Plasma cell‐Free transcriptome profiling in chronic liver disease
Study
EGAS50000000545
-
Identification and Characterization of Cancer Mutations in Japanese LungAdenocarcinoma without Sequencing of Normal Tissue Counterparts
Study
JGAS000001
-
Immuno-genomic Profiling of Biopsy Specimens Predicts Neoadjuvant Chemotherapy Response in Esophageal Squamous Cell Carcinoma
Study
JGAS000535
-
Broad utility of ultrasensitive analysis of ctDNA dynamics across solid tumors treated with immunotherapy
Study
EGAS50000001333
-
Human lymphoid-neutrophil/monocyte restriction co-ordinately activates increased proliferation despite parallel heterogeneity in transcriptional changes
Study
EGAS50000000278
-
Fragmentomics Uncover Non-Mutational HRD Features
Study
EGAS00001008190
-
Djerroudi et al., E-cadherin inactivation shapes tumor microenvironment specificities in invasive lobular carcinoma
Study
EGAS50000000761
-
EGA file encryption types
Documentation
check-encryption-type
-
Reading about genomic analysis of pan-neuroblastoma
Blog
genomic-analysis-of-pan-neuroblastoma
-
Genomic Analyses Identify Recurrent MEF2D Fusions in Acute Lymphoblastic Leukemia
Study
EGAS00001001952
-
Comprehensive analyses of somatic TP53 mutation in tumors with variable mutant allele frequency
Study
EGAS00001002200
-
Population_dynamics_in_abnormal_haematopoiesis
Study
EGAS00001003181
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
-
Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
-
DERMATLAS__Hidradenoma_papilliferum_WES
Study
EGAS00001005714
-
DERMATLAS__Porocarcinoma_WES
Study
EGAS00001005720
-
DERMATLAS__Poroma_RNAseq
Study
EGAS00001005759
-
TGF-β attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells.
Study
EGAS00001002556
-
Clonal hematopoiesis is associated with adverse outcomes in patients with COVID-19
Study
EGAS00001006218
-
Ovarian cancer organoid biobank
Study
EGAS00001003073
-
Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
Study
EGAS00001003206
-
Clinical Cancer Genomic Profiling by Three-Platform Sequencing of Whole Genome, Whole Exome and Transcriptome
Study
EGAS00001002217
-
Mitochondrial-Nuclear Mutational Cross-Talk Drives Recurrence of Localized Prostate Cancer
Study
EGAS00001001782
-
DERMATLAS__Leiomyosarcoma_WES
Study
EGAS00001007628
-
DERMATLAS__Poroma_WES
Study
EGAS00001007705
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_RNAseq
Study
EGAS00001007746
-
Field_effect_of_healthy_and_diseased_livers
Study
EGAS00001002382
-
BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
-
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Study
EGAS00001002606
-
ALPI deficiency causes refractory Inflammation Bowel Disease
Study
EGAS00001003350
-
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers
Study
EGAS00001001112
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH1
Study
EGAS00001001854
-
Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma
Study
EGAS00001005023
-
Interferon lambda 4 impairs viral antigen presentation and attenuates T cell responses
Study
EGAS00001005396
-
The dataset of Southeast Borneo individuals (Banjar and Ngaju ethnic groups) was used as comparative data to determine the Asian parental population of the Malagasy. Our study found strong support for an origin of the Asian ancestry of Malagasy among the Banjar.
Study
EGAS00001001841
-
Comprehensive pharmacogenomic characterization of gastric cancer
Study
EGAS00001004106
-
DERMATLAS__Hidradenoma_papilliferum_RNAseq
Study
EGAS00001005715
-
DERMATLAS__Porocarcinoma_RNAseq
Study
EGAS00001005721
-
Molecular stratification of endometrioid ovarian carcinoma predicts clinical outcome
Study
EGAS00001004366
-
Whole-exome sequencing of glioblastomas with long-term relapse interval
Study
EGAS00001006022
-
DLBCL NGS Genomic Datasets of non-China cohort from Phoenix Clinical Trial
Study
EGAS00001005554
-
Salivary Gland Cancer TSO500 dataset
Study
EGAS00001006232
-
Functional and genomic heterogeneity of long-term self-renewing compartment as the origin of treatment resistance in pancreatic tumors
Study
EGAS00001003442
-
Genetic and epigenetic variation at regulatory regions contribute to cancer evolution under endocrine treatment
Study
EGAS00001006340
-
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer
Study
EGAS00001006466
-
DERMATLAS__Tubular_adenoma
Study
EGAS00001006686
-
DERMATLAS__Tubular_adenoma_RNAseq
Study
EGAS00001006685
-
scRNASeq of human innate lymphoid cells from different compartments
Study
EGAS00001006847
-
Genotype data from 'Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture.'
Study
EGAS00001006944
-
Integrated single cell analysis in transformed follicular lymphoma
Study
EGAS00001007023
-
DERMATLAS__Leiomyoma_WES
Study
EGAS00001007629
-
DERMATLAS__Leiomyoma_RNAseq
Study
EGAS00001007630
-
DERMATLAS__Leiomyosarcoma_RNAseq
Study
EGAS00001007631
-
Endocrine therapy reprogramming of breast cancer facilitates metastatic escape via upregulation of P-Rex1/Rac1 signalling
Study
EGAS00001008353
-
Somatic mutation and selection at epidemiological scale - TwinsUK_RENanoSeq_Buccal
Dataset
EGAD00001015621
-
early-stage ESCC sequencing study
Study
EGAS00001006126
-
Clonally heritable gene expression imparts a layer of diversity within cell types
Study
EGAS50000000161
-
A Pilot Study of Neoadjuvant Nivolumab, Ipilimumab and Intralesional Oncolytic Virotherapy for HER2-Negative Breast Cancer
Study
phs003316
-
A proteogenomic atlas of the human neural retina
Study
EGAS50000000070
-
Dysregulation of Alternative Splicing Is a Transcriptomic Feature of Patient Derived Fibroblasts From CAG Repeat Expansion Spinocerebellar Ataxias
Study
phs003759
-
Translational analyses from a phase II study of pembrolizumab and epigenetic modification with azacitidine in platinum-resistant epithelial ovarian cancer
Study
EGAS50000001165
-
Ensilication as a Cold‑Chain–Free Solution for High‑Fidelity DNA Preservation in tumor samples
Study
EGAS50000001698
-
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
-
multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Study
EGAS00001003651
-
Multi-omic Profiling of Central Nervous System Leukemia Identifies mRNA Translation as a Therapeutic Target
Study
EGAS00001005647
-
Diagnostic utility of whole genome sequencing in adults with B-other acute lymphoblastic leukemia - RNA
Dataset
EGAD00001009305
-
Reliable detection of somatic mutations in solid tissues by laser-capture microdissection and low-input DNA sequencing
Dataset
EGAD00001006088
-
Ancestry and somatic profile predict acral melanoma origin and prognosis – RNA
Dataset
EGAD00001015756
-
TRACERx NSCLC, multiregion sequencing of the first 100 tumors
Dataset
EGAD00001003206
-
Longitudinal profiling of the immune response to Plasmodium vivax in naive hosts by RNA-sequencing
Dataset
EGAD00001006924
-
Bolleboom-Gao peri-tumoral snRNA-seq glioblastoma dataset 2022/A - Data Access Committee
Dac
EGAC00001003049
-
Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis
Study
EGAS00001007008
-
The APL DAC comprises a clinician and biologist who conducted the study.
Dac
EGAC00001000865
-
Single-cell RNA-sequencing reveals that glioblastoma recapitulates a normal neurodevetlopmental hierarchy
Dac
EGAC00001001625
-
PIK3CA mutation in a case of CTNNB1 mutant sinonasal glomangiopericytoma
Study
EGAS00001005653
-
A critical spotlight on the paradigms of FFPE-DNA sequencing
Study
EGAS00001005757
-
A multi-center genome-wide association study for nasopharyngeal carcinoma
Study
EGAS00001006062
-
AVENIO Expanded ctDNA panel sequence alignments (BAMs) from plasma DNA of lung cancer patients from the OSCILLATE trial
Study
EGAS50000000103
-
PGRN/PAT: The genomic basis for susceptibility to drug-induced long QT syndrome (diLQTS)
Study
phs000808
-
Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency
Study
phs002816
-
Genetic Basis of Cryptorchidism
Study
phs000986