-
Somatic mutation and clonal evolution in the human pancreas - WGS (2019-12-17)
Dataset
EGAD00001005751
-
Cell line data (RNAseq, ATACseq, ChIPseq)
Dataset
EGAD00001005493
-
National Eye Institute (NEI) Age-Related Eye Disease Study (AREDS)
Study
phs000001
-
Analysis of Donor Pancreata Defines the Transcriptomic Signature and Microenvironment of Early Neoplastic Pancreatic Lesions
Study
phs003229
-
Genetic Neuroscience: How Human Genes and Alleles Shape Neuronal Phenotypes
Study
phs002032
-
Impact of Genetic Variation on Response to GO Therapy in COG-AML Trials AAML03P1 and AAML0531
Study
phs003490
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
-
Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing
Study
EGAS00001000962
-
The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia
Study
EGAS00001004212
-
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Study
EGAS00001004546
-
Tubulointerstitial fibrosis is the histological hallmark of chronic kidney disease (CKD). Hypoxia and inflammation (i.e., interleukin (IL)-1β signalling) are independent mediators of tubulointerstitial fibrosis. However, the physiological response of human kidney tubular cells to IL-1β/IL-1RI signalling under the hypoxic conditions of CKD is poorly understood and remains a clinical imperative for therapeutic targeting. This study reports that hypoxia and IL-1β act in synergy to trigger cell cycle arrest/cellular senescence of ex vivo patient-derived primary proximal tubular epithelial cells (PTECs).
Study
EGAS00001007904
-
Accurate detection and classification of pediatric sarcomas based on cell-free DNA fragmentation patterns
Study
EGAS00001005127
-
Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models
Study
EGAS00001005596
-
Germline variants in patients with rare cancers and their implications for precision cancer medicine: experiences from the Multicenter MASTER Trial by the German Cancer Consortium (HIPO_021)
Study
EGAS00001005537
-
Leveraging Extended Families for Cardiovascular Disease Genomic Discovery
Study
phs002464
-
Breakpoint detection using long insert whole genome sequencing
Study
phs000646
-
NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Study
phs001217
-
Genome Wide Association Study of Subjects with Myalgic Encephalomyelitis (ME)/Chronic Fatigue Syndrome (CFS)
Study
phs001015
-
Genomic Translation for ALS Care (GTAC) - WGS
Study
phs002973
-
Genomic Analysis of Bevacizumab-induced Hypertension
Study
phs001597
-
A Genome-Wide Association Study for Post-bronchodilator Lung Function in Children with Asthma
Study
phs001216
-
Phenotypic Signatures of Circulating Neoantigen-Reactive CD8+ T Cells in Patients with Metastatic Cancers
Study
phs003064
-
NHLBI TOPMed: Women's Health Initiative (WHI)
Study
phs001237
-
Analysis of TKI resistant mechanism for gastrointstinal stromal tumor
Study
JGAS000039
-
Whole-genome sequencing analysis for understanding of the stepwise progression of lung adenocarcinoma
Study
JGAS000570
-
PanCancer genome analysis in 5143 Japanese cancer patients
Study
JGAS000274
-
Gene expression data of 2D duodenum organoids with or without continuous flow
Study
JGAS000256
-
WES of Mino-VEN-R Mantle Cell Lymphoma Cells
Study
EGAS50000001088
-
PROMETEO
Study
EGAS50000001499
-
Single-nucleus chromatin accessibility profiling of human fetal liver hematopoiesis (10x Multiome)
Study
EGAS50000001632
-
Transcriptional effect of 4HTBZ on Caco-2 cells
Study
EGAS50000001237
-
Single-nucleus gene expression profiling of human fetal liver hematopoiesis (10x Multiome)
Study
EGAS50000001631
-
Optimized large-scale longitudinal biorepository of gastroesophageal adenocarcinoma patient-derived organoids
Study
EGAS50000001614
-
Whole Exome Sequencing of Human Gastro-esophageal Cancer PDXs
Study
EGAS50000000966
-
Papua New Guinean Lowlanders Dataset
Study
EGAS50000000033
-
Paired Biopsy Project: West Coast Dream Team
Study
EGAS50000000327
-
Development of targeted DNA sequencing panel for brain tumors
Study
EGAS50000000699
-
Prime-seq of human term placenta-derived trophoblast organoids
Study
EGAS50000000833
-
scRNA-seq of human follicular lymphoma and lymph node
Dataset
EGAD50000001143
-
Acute_Lymphoblastic_Leukemia_Exome_sequencing_2_
Study
EGAS00001000200
-
Single cell RNA-sequencing (scRNA-seq) of the human hematopoietic stem cell compartment (CD34+CD38-CD45RA-)
Study
EGAS00001004769
-
Whole genome sequencing of colon organoid cultures with artificially induced oncogenic mutations
Study
EGAS00001001969
-
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Study
EGAS00001001422
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom
Study
EGAS00001002257
-
Acute_Lymphoblastic_Leukemia_Exome_sequencing
Study
EGAS00001000201
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000198
-
Exome_sequencing_of_Congenital_Heart_Disease_families_Royal_Brompton
Study
EGAS00001000187
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000199
-
Germline alterations of acute myeloid leukemia
Study
EGAS00001002760
-
DNA Methylation-based diagnostic biomarkers for ESCC in Han Chinese population
Study
EGAS00001003158
-
Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia
Study
EGAS00001003248
-
Acute_Lymphoblastic_Leukemia_Sequencing
Study
EGAS00001000058
-
The NIHR BioResource Rare Diseases BRIDGE consortium sequencing projects
Study
EGAS00001001012
-
Immuno-genomic landscape of osteosarcoma
Study
EGAS00001004197
-
Genome-wide search to find the genetic elements underlying visual contour perception
Study
EGAS00001003639
-
FinHer_Breast_Cancer_Study
Study
EGAS00001000648
-
Genomic Landscape of Pediatric Myelodysplastic Syndromes
Study
EGAS00001002202
-
Gene expression profiling of nasopharyngeal carcinoma
Study
EGAS00001004542
-
Gene_regulation_of_human_CD4__Treg_cells_
Study
EGAS00001003516
-
Immuno-genomic landscape of osteosarcoma
Study
EGAS00001003887
-
The polarity and specificity of antiviral T lymphocyte responses determine susceptibility to SARS-CoV-2 infection in cancer patients and healthy individuals
Dataset
EGAD00001008538
-
Stratton__WGS___Identification_of_Early_Life_Exposures_in_Paediatric_Colonic_Crypts_of_Healthy_Individuals
Study
EGAS00001007921
-
Chromatin activation profiling of stereotyped chronic lymphocytic leukemias reveals a subset #8 specific signature
Study
EGAS00001006457
-
Diagnosis of multisystem inflammatory syndrome in children by a whole-blood transcriptional signature
Study
EGAS00001007409
-
Pharmacogenomic profiling reveals molecular features of chemotherapy resistance in IDH wild type primary glioblastoma
Study
EGAS00001006989
-
KIR gene content imputation from single-nucleotide polymorphisms in the Finnish population
Study
EGAS00001005457
-
A transcriptome atlas of human skeletal muscles
Study
EGAS00001005904
-
CUT&RUN of AML1-ETO binding occupancy following miR-130a KD in Kasumi-1 cells
Study
EGAS00001005867
-
Placebo-only arm transcriptomic analysis of the phase 3 PROTECT clinical trial
Study
EGAS00001006344
-
Genomic variants in 121 genes associated with ovarian cancer in cancer tissue and derived organoids
Dataset
EGAD00001005279
-
FASTQ files of the polyA+ (oligo-dT) RNA-Seq dataset from the POPS SGA (Small for Gestational Age) samples and their matched controls.
Dataset
EGAD00001006304
-
Smart-seq 2 single cell sequencing of CD4 and CD8 T cells from the blood and synovial fluid of 4 psoriatic arthritis patients.
Dataset
EGAD00001006342
-
WES, sWGS and RNA-seq of Asian breast cancer
Dataset
EGAD00001006399
-
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing
Study
phs001700
-
Heart Failure Network - Nitrate's Effect on Activity Tolerance in Heart Failure with Preserved Ejection Fraction (HFN NEAT-BioLINCC)
Study
phs003548
-
Heart Failure Network - Imaging from Nitrate's Effect on Activity Tolerance in Heart Failure with Preserved Ejection Fraction (HFN NEAT-Imaging)
Study
phs004254
-
deCODE Genetics study on genes contributing to nicotine dependence in humans
Study
phs000393
-
Human Lung Tissue eQTL Study
Study
phs001745
-
A New High-Throughput Sequencing-Based Technology to Study Heterochromatin Structure
Study
phs002202
-
Multimodal Mapping of the Immune Landscape in Human Pancreatic Cancer
Study
phs002071
-
Prevention of Viral Hepatitis and HIV in Drug Users - A Hepatitis B Model for HIV and an HB Vaccine Model for HIV Vaccine Trials in Drug Users (DASH)
Study
phs002331
-
TCGA WGS Variants Across 18 Cancer Types
Study
phs003155
-
Somatic Mutations in Epilepsy: Whole Genome Sequence Analysis of Single Neurons
Study
phs002615
-
3.5KJPNv2, an allele frequency panel of 3,552 Japanese individuals
Study
JGAS000159
-
Identifying autosomal recessive mutations causing neurological disorders
Study
EGAS00001000023
-
Transcriptomic analysis of B-cell acute lymphoblastic leukaemia (B-ALL) patients treated on the ALL09 clinical trial
Study
EGAS50000001109
-
Recording physiological history of cells with chemical labeling.
Study
EGAS50000000056
-
Clonal heterogeneity leads to secondary resistance in a melanoma patient after adoptive cell therapy with tumor-infiltrating lymphocytes
Study
EGAS50000000279
-
RNA sequencing data from glioblastoma primary cell lines treated with indisulam
Study
EGAS50000000680
-
Clinical relevance of TCGA subtypes for gastric cancer patients
Study
EGAS50000000779
-
MATISSE bulk RNA-sequencing data
Dataset
EGAD50000001470
-
Inferring causal genes at type 2 diabetes GWAS loci through chromosome interactions in islet cells
Dataset
EGAD50000000517
-
Evolutionary Origins of Recurrent Pancreatic Cancer
Study
EGAS00001004097
-
A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
-
ICGC Oesophageal adenocarcinoma - tumour samples
Study
EGAS00001000725
-
Whole Genome Sequencing of Liver Cancers
Study
EGAS00001002408
-
Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301