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SINGLE CELL ANALYSIS OF IN VITRO ERYTHROPOIESIS
Dataset
EGAD00001000979
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Competitive selection of somatic mutant clones in normal human skin varies with body site
Dataset
EGAD00001006194
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Multiomic characterization of clonotypic B cells
Dataset
EGAD50000002162
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Stage-specific gene and transcript dynamics in human male germ cells
Study
EGAS00001006135
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RNA sequencing data of 142 samples from 142 patients with HER2+ breast cancer treated with letrozole or tamoxifen (SOLTI PAMELA trial)
Study
EGAS00001006410
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scRNA-seq of patient-derived PDAC organoids and matched CAFs
Study
EGAS00001006661
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The molecular landscape of glioma in patients with Neurofibromatosis 1.
Study
EGAS00001003186
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scRNAseq and scATACseq of placebo controlled-trial on MMR non-specific effects
Study
EGAS00001006787
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Spatial and temporal intra-tumoural heterogeneity in advanced High-Grade Serous Ovarian Cancer: implications for surgical and clinical outcomes
Study
EGAS00001007164
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AML FLT3 TCR study
Study
EGAS00001007467
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Non-invasive prenatal diagnosis by genome-wide haplotyping of maternal cell-free plasma DNA
Study
EGAS00001003634
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Whole genome and whole transcriptome sequencing of patients diagnosed with angiosarcoma.
Study
EGAS00001003895
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Mutation signatures in melanocytic nevi reveal characteristics of defective DNA repair
Study
EGAS00001004274
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Human Developmental Biology Resource (HDBR) abnormal fetal samples
Study
EGAS00001006300
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Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004232
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Molecular profiling of EBV associated diffuse large B-cell lymphoma
Study
EGAS00001006400
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Multiple Tissue Monitoring in Huntington disease - RNAseq skeletal muscle
Study
EGAS00001006474
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Alternative lengthening of telomeres in childhood neuroblastoma from genome to proteome
Study
EGAS00001004349
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502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication
Study
EGAS00001002926
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503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Study
EGAS00001002951
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The exomic landscape of t(14,18) negative diffuse follicular lymphoma with 1p36 deletion
Study
EGAS00001002594
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Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population
Study
EGAS00001002641
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Natural variation of circulating RNAs in human serum
Study
EGAS00001002814
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Ibrutinib induces a global chromatin reorganisation in chronic lymphocytic leukaemia
Study
EGAS00001002827
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CCND1-negative MCL
Study
EGAS00001003060
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Primary breast cancers and paired brain metastases sequencing study
Study
EGAS00001003173
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Microsatellite unstable colorectal cancers
Study
EGAS00001003366
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Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
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COMPARE study: participants typed during UK Biobank version 2 array development phase
Study
EGAS00001003748
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Chracterising_cellur_pathways_underlying_CD3_CD28_activation_of_human_CD4__cells
Study
EGAS00001002599
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T-cell reconstitution after reduced dose ATLG induction in kidney transplant recipients
Study
EGAS00001005941
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Comprehensive genomic profiling of matched glioblastoma tumours, cell-lines, and xenografts reveals genomic stability and adaptation to disparate growth environments
Study
EGAS00001002709
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Single cell transcriptomic and genomic profiling of carcinogenesis in patients with familial adenomatous polyposis
Study
EGAS00001003598
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WXS of 147 lung cancer patients treated with immunotherapy
Study
EGAS00001003781
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MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD37920__Targeted_
Study
EGAS00001003321
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Molecular profiling of blastic plasmacytoid dendritic cell neoplasm (BPDCN) as compared to acute myeloid leukemia (AML)
Study
EGAS00001003453
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Single-cell RNA-sequencing reveals that glioblastoma recapitulates a normal neurodevetlopmental hierarchy
Study
EGAS00001004422
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Characterization of four subtypes in morphologically normal tissue excised proximal and distal to breast cancer
Study
EGAS00001004510
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Transcriptomic analysis of the Phase 3 COMPARZ clinical trial
Study
EGAS00001004534
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Whole Genome Sequencing of 317 individuals from the Pacific region
Study
EGAS00001004540
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Indonesian Genome Diversity Project 2
Study
EGAS00001003654
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Ultraviolet radiation drives mutations in a subset of mucosal melanomas
Study
EGAS00001004697
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Genomics_of_acral_lentiginous_melanoma
Study
EGAS00001003740
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HCA_Female_Reproductive_Adult_WSSS_RNA
Study
EGAS00001004727
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NRG1 Fusions in KRAS Wild-type Pancreatic Cancer (H021)
Study
EGAS00001002759
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Genomics_of_acral_lentiginous_melanoma___RNAseq
Study
EGAS00001003758
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Single cell T cell Landscape and T Cell Receptor Repertoire Profiling of AML in Context of PD-1 Blockade Therapy
Study
EGAS00001004894
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Transcriptome sequencing of intravenous leiomyomatosis and uterine myoma
Study
EGAS00001002504
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The aim of this study was to identify underlying hub genes and dysregulated pathways associated with the development of HCC using bioinformatics analysis.
Study
EGAS00001002526
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Progression to AML is predictable and distinct from age related clonal hematopoiesis
Study
EGAS00001002570
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NanoSring of PBMC from bladder cancer and RCC patients
Study
EGAS00001004229
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Transcriptome profiling of human plucked frontal and occipital hair follicles
Study
EGAS00001002832
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Exploring_the_heterogeneity_of_sarcoma_using_single_cell_sequencing_
Study
EGAS00001002866
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Identification of hypermutation and defective mismatch repair in ctDNA from metastatic prostate cancer
Study
EGAS00001003899
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Single cell exome sequencing of lung adenocarcinoma
Study
EGAS00001002972
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Patterns of transcription factor programs and immune pathway activation define four major subtypes of SCLC with distinct therapeutic vulnerabilities
Study
EGAS00001004888
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Whole exome sequencing on Pediatric MDS patients
Study
EGAS00001005432
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Single-cell DNA sequencing on Pediatric MDS
Study
EGAS00001005433
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Benchmarking of ProSolo, a new probabilistic single nucleotide variant caller for single cell DNA sequencing data. This study provides the whole exome sequencing dataset used in this assessment.
Study
EGAS00001004123
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Long cell-free DNA molecules in maternal plasma
Study
EGAS00001005515
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Panbody_nanoseq
Study
EGAS00001005521
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COVID_19_UK_CIC_Spatial
Study
EGAS00001005817
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Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Surname.
Study
EGAS00001002535
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Paediatric_and_adult_nasal_RNAseq___COVID19
Study
EGAS00001004391
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Pathogenic Neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
Study
EGAS00001005530
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Understanding_hematopoietic_stem_cell_mobilization_and_engraftment_
Study
EGAS00001004620
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Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies unique proteotypes associated with patient outcomes
Study
EGAS00001006068
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molecular profiles of serum-derived extracellular vesicles in high-grade serous ovarian cancer
Study
EGAS00001006350
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Juntendo Muscle Study (JMS)
Study
EGAS00001006362
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Muscle SATellite cell study (MSAT)
Study
EGAS00001006363
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SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes
Study
EGAS00001006376
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NOTCH-mutations drive immune-escape mechanisms in B cell malignancies
Study
EGAS00001005793
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Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism
Study
EGAS00001003617
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Multiple Tissue Monitoring in Huntington disease - RNAseq fibroblasts
Study
EGAS00001006472
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Multiple Tissue Monitoring in Huntington disease - RNAseq adipose tissue
Study
EGAS00001006473
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Measurement of SARS-CoV-2 variants fraction in infected alveolar cells
Study
EGAS00001006730
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Characterization of chromatin accessibility in metastatic prostate cancer
Study
EGAS00001006698
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Clinical utility of combined low-pass whole genome and targeted sequencing in liquid biopsies for diagnosis and monitoring of pediatric solid tumors
Study
EGAS00001006913
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Personalized Onco-Genomic Project for pediatric and adolescent patients in British Columbia
Study
EGAS00001006967
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Selective advantage of mutant stem cells in human clonal hematopoiesis is associated with attenuated response to inflammation and aging
Study
EGAS00001007358
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Single-cell proteogenomics of MDS upon AZA
Study
EGAS00001007427
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Subclonal somatic copy number alterations emerge and dominate in recurrent osteosarcoma
Study
EGAS00001007486
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Organ_maturation_in_preparation_for_birth__Peds_RFA__to_develop_a_tissue__resource_and_a_single_cell_atlas_of_organ_development_and_maturation_for__dissemination_among_the_scientific_and_clinical_community__RNA
Study
EGAS00001008256
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Oesophageal adenocarcinoma WGS from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)
Dataset
EGAD00001009400
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T-cell reconstitution after reduced dose ATLG induction in kidney transplant patients
Dataset
EGAD00001008478
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Adult-type Granulosa Cell Tumour of the Ovary RNA Sequencing
Dataset
EGAD00001007812
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Targeted myeloid panel DNA-Sequencing Mutations Matrix Validation Cohort
Dataset
EGAD00001008506
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Bulk RNA sequencing of Singapore colorectal cancer patients (SG-BULK)
Dataset
EGAD00001008512
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Upper cortical layer-driven network impairment in schizophrenia - 10x genomics v3 snRNA-seq and Visium spatial transcriptomics datasets
Dataset
EGAD00001009173
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WES and RNA-seq of triple-negative breast cancers from the MyBrCa cohort
Dataset
EGAD00001009311
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Dataset for the Pearl study
Dataset
EGAD00001007979
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Distinct embryonic phylogenies and driver events of infant Wilms tumor - DNA
Dataset
EGAD00001009812
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Paired-WGS Sequencing of Primary lymphomas of the central nervous system (PCNSL)
Dataset
EGAD00001007806
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Somatic mutation and clonal evolution normal breast tissue WGS
Dataset
EGAD00001010123
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Alloreactive T-cell receptor (TCR) repertoire in kidney transplantation
Dataset
EGAD00001007695
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Dataset for other_cancer-RNA
Dataset
EGAD00001008847
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Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015259
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Single-Cell Atlas of Common Variable Immunodeficiency shows germinal center-associated epigenetic dysregulation in B cell responses
Dataset
EGAD00001008575
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Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Dataset
EGAD00001009280
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Pulmonary atypical carcinoid multi-omic dataset on up to 42 tumours from same patient
Dataset
EGAD00001009296
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Organoid Derivation Project: WGS (2023-06-22)
Dataset
EGAD00001011090
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Single cell transcriptional evolution of myeloid leukaemia of Down syndrome – scRNA
Dataset
EGAD00001015452
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A spatiotemporal cancer cell trajectory underlies glioblastoma heterogeneity
Dataset
EGAD00001015516
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Neuroblastoma patient Total RNA Seq data
Dataset
EGAD00001008124
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An atlas of the developing human fetal spine
Dataset
EGAD00001009801
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Transcriptome analysis for intrahepatic cholangiocarcinoma
Dataset
EGAD00001008544
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RNA-seq data
Dataset
EGAD00001008553
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Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015260
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Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing
Dataset
EGAD00001007794
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DNA methylation changes upon growth hormone treatment in children with idiopathic short stature
Dataset
EGAD00001008641
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Somatic mutations in facial skin from countries of contrasting skin cancer risk
Dataset
EGAD00001009666
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Whole blood RNA sequencing of individuals from Nepal
Dataset
EGAD00001011131
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Whole genome sequencing
Dataset
EGAD00001009746
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Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015257
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Whole blood RNA-sequencing of covid-19 patients and healthy controls
Dataset
EGAD00001007776
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Next Generation Children project
Dataset
EGAD00001007780
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Multiregional single cell RNA sequencing of human renal cell carcinoma
Dataset
EGAD00001008030
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WGS data for manuscript titled: Multi-omic features of oesophageal adenocarcinoma in patients treated with preoperative neoadjuvant therapy
Dataset
EGAD00001008646
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POETIC clinical Trial Ki67 Bookend Breast Cancer Targeted Exome and RNAseq Project
Dataset
EGAD00001010919
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Somatic pathogenic variants in the normal mammary gland of sporadic breast cancer patients
Dataset
EGAD00001008327
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Shallow whole genome sequencing and targeted sequencing of DLBCL patients treated in the HOVON84 trial
Dataset
EGAD00001008389