-
Revealing active mutational processes in tumours using DigiPico/MutLX at unprecedented accuracy
Study
EGAS00001003555
-
Prostate cancer ancestral genomic disparity
Study
EGAS00001006425
-
Genetic Alterations in Benign Breast Biopsies of Subsequent Breast Cancer Patients
Study
EGAS00001003563
-
South Asia Rheumatic Heart Disease Genetics Network
Study
EGAS00001003565
-
SARS-CoV-2 host genetics and COVID-19 outcomes in admixed Brazilians with extreme phenotypes
Study
EGAS00001006376
-
Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia
Study
EGAS00001006819
-
Disease and phenotype relevant genetic variants identified from histone acetylomes in human hearts
Study
EGAS00001003586
-
Multimodal Epigenetic Sequencing Analysis (MESA) of Cell-free DNA for Non-invasive Cancer Detection
Study
EGAS00001006462
-
5- FU treated organoids
Study
EGAS00001003592
-
Dedifferentiated_Melanoma_RNAseq
Study
EGAS00001003601
-
GDAP___Genome_Diversity_in_Africa_Project
Study
EGAS00001003602
-
Discovery and capture of novel dynamic DNA methylation in human sperm with preferential links to altered folate metabolism
Study
EGAS00001003617
-
Transcriptome profiling of three giant cell tumour of bone cell lines
Study
EGAS00001006441
-
Cystic fibrosis multi-omics study
Study
EGAS00001006421
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
Genetic regulation of RNA splicing in human pancreatic islets
Study
EGAS00001006440
-
GWAS Results from Danjou et al, Nature Genetics 2015
Study
EGAS00001003645
-
Genomic analysis and evolutionary modeling of breast and larynx cancer, based on specimens from Polish population
Study
EGAS00001006456
-
Human adipose tissue immune cells
Study
EGAS00001003725
-
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer
Study
EGAS00001006466
-
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Study
EGAS00001004943
-
Genetic insights into the biological mechanisms governing human ovarian ageing
Study
EGAS00001004947
-
Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma
Study
EGAS00001003746
-
Host pathogen interaction long read transcriptome
Study
EGAS00001006779
-
Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients
Study
EGAS00001006490
-
Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort
Study
EGAS00001006870
-
Immune microenvironment and lineage tracing help deciphering Rosette-forming GlioNeuronal Tumors: a multi-omic analysis of 9 cases
Study
EGAS00001006502
-
Genetic variants of the COL4A3, COL4A4, and COL4A5 genes contribute to thinned glomerular basement membrane lesions in sporadic IgA nephropathy patients
Study
EGAS00001006519
-
Neuroblastoma Evolution
Study
EGAS00001006533
-
Epigenetic and metabolomic data from type 2 diabetes adolescents
Study
EGAS00001003816
-
cfDNA in Hereditary And High-Risk Malignancies (CHARM)
Study
EGAS00001006539
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Study
EGAS00001006904
-
Gene copy number variation in pediatric mental illness in a general population
Study
EGAS00001006659
-
Single-cell ATAC-seq analysis for COVID19 patients
Study
EGAS00001006559
-
Single-cell RNA-seq analysis for COVID19 patients
Study
EGAS00001006560
-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006945
-
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Study
EGAS00001004020
-
Multiome_HB
Study
EGAS00001006932
-
CYP2C19 long-read sequencing
Study
EGAS00001006929
-
Genomic_characterisation_of_MGUS__
Study
EGAS00001004124
-
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform, P49-P104 and run1 replicates
Study
EGAS00001006595
-
Whole exome sequencing identifies clinically relevant mutational signatures in resected hepatocellular carcinoma
Study
EGAS00001004371
-
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures (Hipo_021)
Study
EGAS00001006629
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Study
EGAS00001006631
-
Nasal epithelial cells of PCD and non-PCD patients grown at air-liquid interface for RNAseq analysis
Study
EGAS00001006632
-
Search for genetic variants influencing gestational weight gain in type 1 diabetes patients by genome wide association method
Study
EGAS00001004408
-
H3Africa - Trauma And Neurobiology: Maternal stress and transgenerational impact. Search for Epigenetic Markers
Study
EGAS00001006645
-
DNA methylation landscape of prostate cancer
Study
EGAS00001006670
-
Follicular lymphoma at diagnosis, treated in first line with immunochemotherapy
Study
EGAS00001006674
-
DERMATLAS__Tubular_adenoma_RNAseq
Study
EGAS00001006685
-
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Study
EGAS00001006692
-
HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA
Study
EGAS00001006981
-
Hexanucleotide repeat expansions in C9orf72 alter microglial responses and prevent a coordinated glial reaction in ALS
Study
EGAS00001006711
-
DNA methylation-based classification of sinonasal tumors [Proteomics data]
Study
EGAS00001006712
-
single-stranded DNA study
Study
EGAS00001005093
-
DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Study
EGAS00001006713
-
Chromatin landscape of medulloblastoma reveals context dependent driver
Study
EGAS00001006741
-
The Iberian Roma genetic variant server
Study
EGAS00001006758
-
Molecular heterogeneity and commonalities in pancreatic cancer precursors with gastric and intestinal phenotype
Study
EGAS00001006793
-
Whole-genome sequencing across 449 samples spanning 47 ethnolinguistic groups provides insights into genetic diversity in Nigeria
Study
EGAS00001007036
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Study
EGAS00001007045
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq
Study
EGAS00001006866
-
Timing chromosomal amplification events using patterns of somatic mutations in high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001007052
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation
Study
EGAS00001006881
-
Genotype data from 'Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture.'
Study
EGAS00001006944
-
cis-eQTL mapping of TB-T2D comorbidity in a five-way admixed SA cohort
Study
EGAS00001007059
-
The multifaceted genomic history of Ashaninka from Amazonian Peru
Study
EGAS00001006958
-
Genome wide variation in the Angolan Namib desert reveals unique Pre-Bantu ancestry
Study
EGAS00001007011
-
Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Study
EGAS00001005430
-
Genetic heritage of the Baphuthi highlights an over-ethnicised notion of 'Bushman' in the Maloti-Drakensberg, southern Africa
Study
EGAS00001007080
-
Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma.
Study
EGAS00001007053
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Long-term organoid culture of a small intestinal neuroendocrine tumor
Study
EGAS00001007093
-
Epigenetic landscape of mixed phenotype leukemias
Study
EGAS00001007094
-
Genetic Determinants of Transcriptional Variation in Primary Human Monocytes Across Multiple Contexts
Study
EGAS00001007111
-
Effects of 2DG, Galactose, or Oligomycin on the epigenome remodeling induce by T cells activation.
Study
EGAS00001007115
-
RNAseq
Study
EGAS00001007165
-
Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse
Study
EGAS00001007128
-
IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Study
EGAS00001007144
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001007173
-
Chip_seq_oesophageal_adenocarcinoma_
Study
EGAS00001007180
-
Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
-
The genetic history of the southern Andes from present-day Mapuche ancestry
Study
EGAS00001007200
-
scRNAseq for patients with immunodeficiency and HCs
Study
EGAS00001007271
-
Cohesin Mutations in AML
Study
EGAS00001007405
-
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types
Study
EGAS00001007412
-
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types (RNAseq)
Study
EGAS00001007428
-
Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783
-
HSP90 inhibitor resistant cell line
Study
EGAS00001006381
-
Clinical and genetic factors associated with tumor response to neoadjuvant (chemo)radiotherapy, survival and recurrence risk in rectal cancer
Study
EGAS00001007501
-
Whole genome sequencing of 108 epileptic patients from CENet cohort
Study
EGAS00001007507
-
Single cell transcriptomic landscape of pediatric B-cell acute lymphoblastic leukemia: dissection of transcriptional heterogeneity and B-cell developmental state
Study
EGAS00001007512
-
AfricanNeo aDNA Study
Study
EGAS00001007519
-
Genomic profiling of IBC
Study
EGAS00001007520
-
Massively parallel functional dissection of schizophrenia associated non-coding genetic variants
Study
EGAS00001007542
-
Oxidative phosphorylation is a key ontogenetic feature of monocyte immunometabolism promoting myeloid differentiation after birth
Study
EGAS00001007555
-
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Study
EGAS00001007573
-
DNA-methylation variability in normal mucosa of patients with adenomatous polyps: a marker of field cancerization
Study
EGAS00001007666
-
GOSH_Childhood_Leukemia_Behjati_WellcomeCore_RNA
Study
EGAS00001007616