-
Dataset with genome-wide array data from Algerian Amazigh (Chaoui and Mozabite) and non-Amazigh individuals
Study
EGAS00001007235
-
Long-term temporal stability of peripheral blood DNA methylation alterations in patients with inflammatory bowel disease.
Study
EGAS00001006501
-
Genetic and epigenetic variation at regulatory regions contribute to cancer evolution under endocrine treatment
Study
EGAS00001006340
-
Insights from genome-wide data from Thailand and Laos
Study
EGAS00001006053
-
ATAC-seq/ChIP part
Study
EGAS00001006520
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
Genetic regulation of RNA splicing in human pancreatic islets
Study
EGAS00001006440
-
Transcriptome profiling of three giant cell tumour of bone cell lines
Study
EGAS00001006441
-
Genomic analysis and evolutionary modeling of breast and larynx cancer, based on specimens from Polish population
Study
EGAS00001006456
-
Histone modifications of cfDNA
Study
EGAS00001006503
-
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer
Study
EGAS00001006466
-
Data containing genome-wide SNP data from Northwestern Amazonia
Study
EGAS00001006767
-
Single-cell RNA sequencing reveals the mesangial identity and species diversity of glomerular cell transcriptomes
Study
EGAS00001004943
-
Capturing sex-specific and infertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome
Study
EGAS00001006643
-
Genetic insights into the biological mechanisms governing human ovarian ageing
Study
EGAS00001004947
-
Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients
Study
EGAS00001006490
-
Immune microenvironment and lineage tracing help deciphering Rosette-forming GlioNeuronal Tumors: a multi-omic analysis of 9 cases
Study
EGAS00001006502
-
DERMATLAS__Tubular_adenoma
Study
EGAS00001006686
-
Genetic variants of the COL4A3, COL4A4, and COL4A5 genes contribute to thinned glomerular basement membrane lesions in sporadic IgA nephropathy patients
Study
EGAS00001006519
-
cfDNA in Hereditary And High-Risk Malignancies (CHARM)
Study
EGAS00001006539
-
Single-cell ATAC-seq analysis for COVID19 patients
Study
EGAS00001006559
-
Single-cell RNA-seq analysis for COVID19 patients
Study
EGAS00001006560
-
BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Study
EGAS00001006663
-
Host pathogen interaction long read transcriptome
Study
EGAS00001006779
-
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform, P49-P104 and run1 replicates
Study
EGAS00001006595
-
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
-
Gene copy number variation in pediatric mental illness in a general population
Study
EGAS00001006659
-
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
-
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
-
DNA methylation-based classification of sinonasal tumors [DNA sequencing]
Study
EGAS00001006713
-
single-stranded DNA study
Study
EGAS00001005093
-
Chromatin landscape of medulloblastoma reveals context dependent driver
Study
EGAS00001006741
-
The Iberian Roma genetic variant server
Study
EGAS00001006758
-
Erythroid/megakaryocytic differentiation confers BCL-XL dependency and venetoclax resistance in acute myeloid leukemia
Study
EGAS00001006819
-
Molecular heterogeneity and commonalities in pancreatic cancer precursors with gastric and intestinal phenotype
Study
EGAS00001006793
-
Exome sequencing of HCV+ lymphoma
Study
EGAS00001006860
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities WGS
Study
EGAS00001006865
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities RNA-Seq
Study
EGAS00001006866
-
Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort
Study
EGAS00001006870
-
Atypical teratoid/rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities DNA-Methylation
Study
EGAS00001006881
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Study
EGAS00001006904
-
CYP2C19 long-read sequencing
Study
EGAS00001006929
-
Multiome_HB
Study
EGAS00001006932
-
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
-
Genotype data from 'Dense sampling of ethnic groups within African countries reveals fine-scale genetic structure and extensive historical admixture.'
Study
EGAS00001006944
-
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
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067
-
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
-
Genetic Determinants of Transcriptional Variation in Primary Human Monocytes Across Multiple Contexts
Study
EGAS00001007111
-
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
-
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
-
Mapping the epigenomic landscape of human monocytes following innate immune activation reveals context-specific mechanisms driving endotoxin tolerance
Study
EGAS00001007362
-
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 and transcriptomic landscape of T-cell lymphoblastic lymphoma compared to T-cell acute lymphoblastic leukemia: similar subtypes and different fusions
Study
EGAS00001007767
-
Clinical and genetic factors associated with tumor response to neoadjuvant (chemo)radiotherapy, survival and recurrence risk in rectal cancer
Study
EGAS00001007501
-
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
-
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
-
This study aims to evaluate the relationship between cardiometabolic risk factors and the most common genetic variation (SNPs)
Study
EGAS00001007818
-
The University of Hong Kong Intestinal Metaplasia Organoids Study
Study
EGAS00001007899
-
Phosphoproteomics adds value to treatment recommendations in molecular tumor boards
Study
EGAS00001007891
-
Northern Ireland COhort for the Longitudinal study of Ageing
Study
EGAS00001007915
-
Epi2Diag
Study
EGAS00001008070
-
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