-
Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006945
-
The multifaceted genomic history of Ashaninka from Amazonian Peru
Study
EGAS00001006958
-
HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA
Study
EGAS00001006981
-
Genome wide variation in the Angolan Namib desert reveals unique Pre-Bantu ancestry
Study
EGAS00001007011
-
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
EGAS00001007027
-
Germline genome sequencing samples from the Hereditary Cancer Syndromes (ICCon) Cancer Flagship
Study
EGAS00001007045
-
Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma.
Study
EGAS00001007053
-
cis-eQTL mapping of TB-T2D comorbidity in a five-way admixed SA cohort
Study
EGAS00001007059
-
Genetic heritage of the Baphuthi highlights an over-ethnicised notion of 'Bushman' in the Maloti-Drakensberg, southern Africa
Study
EGAS00001007080
-
Long-term organoid culture of a small intestinal neuroendocrine tumor
Study
EGAS00001007093
-
Epigenetic landscape of mixed phenotype leukemias
Study
EGAS00001007094
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Spatial and temporal transcriptomics of medulloblastoma with chromothripsis identifies multiple genetic clones that resist to treatment and lead to relapse
Study
EGAS00001007128
-
Genetic Determinants of Transcriptional Variation in Primary Human Monocytes Across Multiple Contexts
Study
EGAS00001007111
-
IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Study
EGAS00001007144
-
RNAseq
Study
EGAS00001007165
-
Chip_seq_oesophageal_adenocarcinoma_
Study
EGAS00001007180
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
The genetic history of the southern Andes from present-day Mapuche ancestry
Study
EGAS00001007200
-
Genetic scoring guide for personalized risk assessment in pediatric B-cell precursor Acute Lymphoblastic Leukemia
Study
EGAS00001007239
-
scRNAseq for patients with immunodeficiency and HCs
Study
EGAS00001007271
-
HSP90 inhibitor resistant cell line
Study
EGAS00001006381
-
Whole genome sequencing of 108 epileptic patients from CENet cohort
Study
EGAS00001007507
-
'IL-17A-Producing ILC3s and Duodenal Adenoma in FAP'
Study
EGAS00001007347
-
High-resolution, patient-level dissection of IL-23 blockade in cutaneous psoriasis
Study
EGAS00001007373
-
Analysis of the Elements Involved in the Enrichment of a Panel of Genomic Regions by Nanopore Sequencing Using Adaptive Sampling
Study
EGAS00001007375
-
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types
Study
EGAS00001007412
-
Cohesin Mutations in AML
Study
EGAS00001007405
-
Single-cell proteogenomics of MDS upon AZA
Study
EGAS00001007427
-
Genomic evolution and transcriptional changes in the evolution of prostate cancer into neuroendocrine and ductal carcinoma types (RNAseq)
Study
EGAS00001007428
-
Clinical and genetic factors associated with tumor response to neoadjuvant (chemo)radiotherapy, survival and recurrence risk in rectal cancer
Study
EGAS00001007501
-
AfricanNeo aDNA Study
Study
EGAS00001007519
-
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
-
DERMATLAS__Leiomyoma_WES
Study
EGAS00001007629
-
GOSH_Childhood_Leukemia_Behjati_WellcomeCore_RNA
Study
EGAS00001007616
-
DERMATLAS__Leiomyoma_RNAseq
Study
EGAS00001007630
-
DERMATLAS__Leiomyosarcoma_RNAseq
Study
EGAS00001007631
-
DNA-methylation variability in normal mucosa of patients with adenomatous polyps: a marker of field cancerization
Study
EGAS00001007666
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Study
EGAS00001007703
-
Myeloid-specific KDM6B inhibition sensitizes Glioblastoma to PD1 blockade
Study
EGAS00001007002
-
Genomic and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Study
EGAS00001007767
-
This study aims to evaluate the relationship between cardiometabolic risk factors and the most common genetic variation (SNPs)
Study
EGAS00001007818
-
Phosphoproteomics adds value to treatment recommendations in molecular tumor boards
Study
EGAS00001007891
-
The University of Hong Kong Intestinal Metaplasia Organoids Study
Study
EGAS00001007899
-
Northern Ireland COhort for the Longitudinal study of Ageing
Study
EGAS00001007915
-
Transcriptomics-driven classification of ALAL
Study
EGAS00001007967
-
Single-cell atlas of > 1.5 million PBMC with multi-layer omics data in Japanese
Study
EGAS00001008016
-
Patient-derived tumoroids from CIC::DUX4 rearranged sarcoma identify MCL1 as a therapeutic target
Study
EGAS00001008039
-
Genetic origins of the Kiritimati population from central-eastern Micronesia
Study
EGAS00001008060
-
Dataset with genome-wide array data from Algerian Amazigh (Chaoui and Mozabite) and non-Amazigh individuals
Study
EGAS00001007235
-
Single cell TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008161
-
OMKar
Study
EGAS00001008245
-
H3Africa - Deciphering Developmental Disorders in Africa
Study
EGAS00001008319
-
Genome-wide methylation detection and episignature analysis using PacBio long-read sequencing
Study
EGAS00001008250
-
Osteosarcoma 3D patient derived cultures to test genome-informed personalized treatment options; a feasibility study
Study
EGAS50000001583
-
Whole-exome variant calling of individuals from the study of sepsis and acute distress respiratory syndrome in Spain
Study
EGAS50000001119
-
Multi-omic analysis of Down Syndrome in thyroid
Study
EGAS00001007677
-
Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
Study
EGAS50000001042
-
MorphoITH: A Framework for Deconvolving Intra-Tumor Heterogeneity Using Tissue Morphology
Study
EGAS50000001064
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Mutagen_treated_organoids
Study
EGAS00001004873
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__organoid_control_WGS
Study
EGAS00001005449
-
MutWP1__CRUK_Grand_Challenge__normal_kidney_Nanoseq
Study
EGAS00001005451
-
MutWP1__CRUK_Grand_Challenge__matched_blood_Nanoseq
Study
EGAS00001006774
-
Epigenetics Imagine Arrays
Dac
EGAC00001003633
-
BE_screens_of_WRN_gene_in_MSI_models
Study
EGAS00001006872
-
Discordant_Monozygotic_Twins_ALS (Epigenetics)
Study
EGAS00001008053
-
Discordant_Monozygotic_Twins_ALS (Epigenetics)
Dataset
EGAD00010002716
-
Single-nuclei histone modification profiling of the adult human central nervous system unveils epigenetic memory of developmental programs
Study
EGAS50000000283
-
Reference epigenomes generated as part of the International Human Epigenomics Consortium (IHEC)
Study
EGAS00001000552
-
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Study
EGAS00001002606
-
Human islet 3D chromatin maps provide insights into type 2 diabetes
Study
EGAS00001002917
-
Immune cell atlas of environmental and ancestral diversity in Indonesia [scRNAseq]
Study
EGAS50000001656
-
Immune cell atlas of environmental and ancestral diversity in Indonesia [WGS]
Study
EGAS50000001655
-
Immune Cell Atlas of Environmental and Ancestral Diversity in Indonesia [TCR]
Dataset
EGAD50000002383
-
Immune Cell Atlas of Environmental and Ancestral Diversity in Indonesia [WGS]
Dataset
EGAD50000002384
-
Immune Cell Atlas of Environmental and Ancestral Diversity in Indonesia [scRNAseq]
Dataset
EGAD50000002385
-
Peruvian Population Genomics: Unraveling the Genetic Landscape and Admixture Dynamics of Urban Populations
Study
EGAS00001008264
-
Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance
Study
EGAS00001007362
-
miRNA-seq of paired Follicular Lymphoma (FL) patient samples before and after high-grade transformation to DLBCL (FL vs. tFL) from FFPE tissues
Study
EGAS50000000942
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067
-
mRNA-seq of paired Follicular Lymphoma (FL) patient samples before and after high-grade transformation to DLBCL (FL vs. tFL) from FFPE tissues
Study
EGAS50000000941
-
Context-specific regulatory genetic variation in MTOR dampens neutrophil-T cell crosstalk in pneumonia-associated sepsis, modulating disease
Study
EGAS50000000894
-
A conserved enhancer in ecDNA-containing Medulloblastoma
Study
EGAS50000001609
-
Global RNA sequencing data of human iPSC-derived microglia from frontotemporal dementia (FTD) patients
Study
EGAS50000001688
-
Global RNA sequencing data of human iPSC-derived microglia from frontotemporal dementia (FTD) patients
Dataset
EGAD50000002423
-
McGill Cancer Genetics Predisposition Data Access Committee
Dac
EGAC50000000954
-
Taste Receptor Gene Variants: Body Mass Index (BMI) and Longevity
Study
EGAS00001008403
-
Solid_WXS_MET-XEN
Dataset
EGAD00001002106
-
Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi-Ethnic Samples (T2D-GENES)
Dataset
EGAD00001002246
-
MutWP1: CRUK Grand Challenge Mutographs of Cancer: Colorectal_LCM (2020-02-20)
Dataset
EGAD00001005994
-
MutWP1: CRUK Grand Challenge Mutographs of Cancer: Oesophageal adenocarcinoma
Dataset
EGAD00001006083
-
GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes
Dataset
EGAD00001002247
-
Competitive selection of somatic mutant clones in normal human skin varies with body site
Dataset
EGAD00001006194
-
Blueprint: A human variation panel of genetic influences on epigenomes and transcriptomes in three immune cell types, (ChIP-Seq for CD14-positive, CD16-negative classical monocyte, on genome GRCh37)
Dataset
EGAD00001002672
-
Somatic mutations and single cell transcriptomes reveal the root of malignant rhabdoid tumours
Dataset
EGAD00001006296
-
A comprehensive characterisation and analysis of human breast cancers through whole-genome sequencing
Dataset
EGAD00001002740
-
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Dataset
EGAD00001006151
-
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients with Advanced Lung Adenocarcinoma
Dataset
EGAD00001006287
-
IBD Whole Genome Sequencing (2019-04-01)
Dataset
EGAD00001004880