-
MorphoITH: A Framework for Deconvolving Intra-Tumor Heterogeneity Using Tissue Morphology
Study
EGAS50000001064
-
Nanopore sequencing of FSHD, BAMS and healthy control fibroblast cell lines
Study
EGAS50000001065
-
High Altitude Pulmonary Hypertension
Study
EGAS00001003171
-
Spatial Dynamics of the Developing Heart (single-cell)
Study
EGAS50000001029
-
Population_dynamics_in_abnormal_haematopoiesis
Study
EGAS00001003181
-
Dynamics of Tumor Heterogeneity from Primary to Metastatic Dissemination in Prostate Cancer
Study
EGAS50000000524
-
Whole genome shotgun sequencing and somatic mutations data in Hepatocellular carcinoma
Study
EGAS00001002578
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
Epigenetic reprogramming shapes monocytes and heterologous T cell derived cytokine responses in BCG vaccination
Study
EGAS00001007498
-
Clonal expansion and epigenetic reprogramming following deletion or amplification of mutant IDH
Study
EGAS00001002618
-
Pancreatic cancer organoids recapitulate disease and allow personalized drug screening
Study
EGAS00001003369
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
STREP GENE: Genetics and Severe Streptococcal Infections
Study
EGAS00001003421
-
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
-
Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033)
Study
EGAS00001003481
-
MutWP5__CRUK_Mutographs_of_Cancer__Lung__PD43291_Novaseq__WG_
Study
EGAS00001003502
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Study
EGAS00001003524
-
Khoe-San Genome Project
Study
EGAS50000001408
-
Global RNA sequencing data of human iPSC-derived microglia from frontotemporal dementia (FTD) patients
Study
EGAS50000001688
-
Whole genome sequencing data of paediatric hyperdiploid acute lymphoblastic leukemia
Study
EGAS50000001690
-
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___Exome__Novaseq_
Study
EGAS00001003526
-
A_study_of_the_molecular_pathogenesis_of_Splenic_Marginal_Zone_and_Diffuse_Large_B_Cell_Lymphoma
Study
EGAS00001000335
-
South Asia Rheumatic Heart Disease Genetics Network
Study
EGAS00001003565
-
Pediatric Whole Genome Sequencing Diagnostic Utility
Study
EGAS00001001623
-
Indonesian methylation data
Study
EGAS00001003653
-
Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation
Study
EGAS00001003684
-
The 3D evolution of glioma cell populations
Study
EGAS00001003710
-
Genomic, transcriptomic and epigenomic profiling of GCTB
Study
EGAS00001003730
-
Multi-omic analyses from a randomized phase II study of epigenetic priming followed by nivolumab in previously treated metastatic non-small cell lung cancer
Study
EGAS50000000913
-
An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia (CML)
Study
EGAS00001001751
-
DNA methylation and transposable element landscapes define human regulatory T cells in tissues and identify their blood recirculating counterpart
Study
EGAS50000000738
-
H3K27me3-mediated epigenetic repression regulates neuroblastoma development and contributes to biological heterogeneity
Study
EGAS00001008225
-
A targeted gene panel that covers coding, noncoding, and short tandem repeat regions improves the diagnosis of patients with neurodegenerative diseases
Study
EGAS00001003737
-
Patient-Derived Lung Cancer Organoid
Study
EGAS00001003786
-
Translational analyses from a phase II study of pembrolizumab and epigenetic modification with azacitidine in platinum-resistant epithelial ovarian cancer
Study
EGAS50000001165
-
RNA-seq data in hMPC, MSC_Pat and EWIma
Study
EGAS50000001173
-
Sequencing of an organoid biobank for childhood kidney cancers that captures disease and tissue heterogeneity.
Study
EGAS00001003853
-
IDH-wildtype untreated human glioblastoma samples (GB-UK cohort), published in Noorani & Haughey et al 2025.
Study
EGAS00001008126
-
Genomic and epigenomic characterization of juvenile myelomonocytic leukemia (JMML)
Study
EGAS00001002511
-
Germline variants in UHRF1 are associated with multi-locus imprinting disturbance in humans and mice
Study
EGAS50000001179
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
Organoid cultures of early-onset colorectal cancers reveal distinct and rare genetic profiles
Study
EGAS00001004063
-
BE_screens_of_WRN_gene_in_MSI_models
Study
EGAS00001006872
-
Evolutionary Origins of Recurrent Pancreatic Cancer
Study
EGAS00001004097
-
CD8+ T-cell exhaustion induced by leukemic cells drives progression in Chronic Lymphocytic Leukemia
Study
EGAS00001004116
-
Feasibility study of enzymatic methylation sequencing of cell-free DNA from cerebrospinal fluid of pediatric brain tumors for classification
Study
EGAS50000000871
-
Whole exome sequencing of Parkinson's disease patients from the United Kingdom
Study
EGAS00001002156
-
Epigenetic and transcriptional profile of memory B cells in Multiple sclerosis
Study
EGAS50000000872
-
A Comprehensive Genetic Study of Classical Hodgkin Lymphoma Using Circulating Tumour DNA
Study
EGAS50000000873
-
Targets of MEK inhibition in DIPG
Study
EGAS00001004495
-
Genetic and Microenvironmental Analysis of Peripheral T-cell Lymphoma
Study
EGAS50000001258
-
SNP array files, IDAT files, from 34 members of a Family with a high prevalence of psychosis
Study
EGAS00001004592
-
Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Study
EGAS00001004733
-
The genetic structure of Norway
Study
EGAS00001004826
-
Young Boost Trial for Breast Cancer patients
Study
EGAS50000000797
-
Impact of Glycolysis Inhibition on the Epigenome of Synovial Fluid T Cells in Juvenile Idiopathic Arthritis
Study
EGAS50000000808
-
MethylBERT enables read-level DNA methylation pattern identification and tumour deconvolution using a Transformer-based model
Study
EGAS50000000806
-
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Study
EGAS00001000865
-
Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783
-
Canadian Prostate Cancer Genome Network
Study
EGAS00001000900
-
ATAC-Seq and CTCF ChIP-Seq on the OCIAML-2 cell line
Study
EGAS00001004741
-
Discordant_Monozygotic_Twins_ALS(Genetics)
Study
EGAS50000000908
-
WES samples of patients with anti-PD-1 resistant HNSCC from a non-randomized, open-label phase 1b clinical trial
Study
EGAS50000000729
-
Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
-
A GWAS study with the AlpeDPD study cohort
Study
EGAS00001007855
-
Transcriptional and epigenetic profiling of bone marrow blood progenitors across age
Study
EGAS50000001623
-
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
-
Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
-
A benchmark of DNA methylation deconvolution methods for tumoral fraction estimation using DecoNFlow
Study
EGAS50000001529
-
ATAC-seq, H3K27ac CUT&Tag, and UMI-4C in LCLs derived from constitutional MLH1 epimutation carriers and non-carrier relatives
Study
EGAS50000000499
-
Pediatric Papillary Thyroid Carcinoma Whole Exome Sequencing
Study
EGAS00001005187
-
HipSci HumanExome BeadChip analysis - monogenic diabetes
Study
EGAS00001001273
-
Comprehensive Deep Sequencing Atlas in HCC tumors
Study
EGAS00001007694
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
DERMATLAS__SG_basal_cell_adenoma_and_adenocarcinoma_WES
Study
EGAS00001007745
-
HipSci_RNASEQ_Battens
Study
EGAS00001001987
-
HipSci_RNASEQ_Ataxia
Study
EGAS00001001992
-
MutWP1__CRUK_Grand_Challenge__normal_kidney_Nanoseq
Study
EGAS00001005451
-
T2D-GENES: Exome sequencing
Study
EGAS00001001460
-
HipSci_RNASEQ_BPD
Study
EGAS00001001993
-
HipSci_RNASEQ_Hypertrophic_Cardiomyopathy
Study
EGAS00001001994
-
Transcriptomic and epigenetic characterization of ex vivo expanded T cells
Study
EGAS50000001718
-
TRACERx 100: metastatic samples
Study
EGAS00001002415
-
HipSci___Whole_Exome_sequencing___Cardiomyopathy
Study
EGAS00001001980
-
HipSci_RNASEQ_Congenital_hyperinsulinia
Study
EGAS00001001988
-
HipSci_RNASEQ_Macular_Dystrophy
Study
EGAS00001001995
-
Knoll et al.: The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation
Study
EGAS00001007461
-
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Double mutant DNMT3A AML: a unique subtype
Study
EGAS00001007966
-
Monosomy 7 delineates a primitive acute myeloid leukemia with adverse prognosis and responsiveness to epigenetic therapy
Study
EGAS50000001641
-
HipSci HumanExome BeadChip analysis - Kabuki syndrome
Study
EGAS00001002007
-
AGECAN - Interespecies conservation of brain specific DNA methylation in aging and cancer
Study
EGAS00001004851
-
HipSci HumanExome BeadChip analysis - Macular Dystrophy
Study
EGAS00001002014
-
WES analysis of a mixed cohort of pituitary tumors
Study
EGAS00001001714
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
-
The_Little_Princess_Knowledge_Bank_RNAseq
Study
EGAS00001005244
-
Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE)
Study
EGAS00001003662
-
Single-nucleus ATAC sequencing of the human motor cortex
Study
EGAS50000001563