-
ChIP-seq data of Hodgkin lymphoma cell line L-428
Study
EGAS00001003033
-
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000551
-
Microbial signatures and innate immune gene expression in lamina propria phagocytes of inflammatory bowel diseases patients
Study
EGAS00001003105
-
Harnessing_transposons_for_drug_resistance_gene_discovery_in_cancer
Study
EGAS00001000468
-
Breast_Cancer_Whole_Genome_Sequencing
Study
EGAS00001000210
-
Triple_Negative_Breast_Cancer_RNA_Sequencing
Study
EGAS00001000377
-
Moles
Study
EGAS00001000789
-
Multisite_Primary_Breast_Cancer
Study
EGAS00001000891
-
GWAS and Meta-analysis on Frontal Fibrosing Alopecia in two European Populations
Study
EGAS00001003460
-
WGS bam
Study
EGAS00001005159
-
Blueprint RNAseq profile of purified plasma cells from multiple myeloma patients and tonsils of healthy donors
Study
EGAS00001001110
-
G3BP2-KIT drives leukemia amenable to kinase inhibition in Ph-like ALL
Study
EGAS00001005181
-
BLUEPRINT Epigenetic characterization of megakaryocytes and erythroblasts
Study
EGAS00001001641
-
Variants from a subset of genes from WES of adult AML patient samples
Study
EGAS00001006185
-
BCL11B enhancer hijacking defines a subtype of lineage ambiguous stem cell leukemia
Study
EGAS00001004810
-
Whole-transcriptome sequencing of hepatocellular carcinoma biopsies (TACE study)
Study
EGAS00001005558
-
eccDNA in maternal plasma
Study
EGAS00001003827
-
WES bam
Study
EGAS00001005160
-
arrayCGH for copy number profiling on tumor DNA from pediatric cancer tissue samples
Study
EGAS00001005197
-
Molecular programs of melanoma brain metastases (MBM)
Study
EGAS00001005976
-
COIN CRC GWAS data
Study
EGAS00001005421
-
GWAS in bullous pemphigoid in Germans
Study
EGAS00001004627
-
NLG-LBC-05 ctDNA
Study
EGAS00001005835
-
Dedifferentiated_Melanoma
Study
EGAS00001003471
-
INDIA
Study
EGAS00001006417
-
RNAseq of liver harvested from CDAHFD mice treated for 8 weeks with either the MGAT2 inhibitor compound BMS-963272 or vehicle
Study
EGAS00001006583
-
Comprehensive de novo variant discovery with HiFi long-read sequencing
Study
EGAS00001006479
-
TB-DAR Genotyping Study
Study
EGAS00001007216
-
HCA_Thymus_Paediatric_ThyDesign_RNA_Managed_Access
Study
EGAS00001007687
-
Single-cell analysis of matched FFPE and frozen tissue samples reveals comparable resolution of intratumoural heterogeneity
Dataset
EGAD00001015781
-
Combined DNA Methylation and Genotyping via scTAMARA-seq (DNA)
Dataset
EGAD00001015496
-
RNAseq Atlas in HCC tumors
Dataset
EGAD00001015341
-
RNA-seq dataset of Oncogenic and immunological targets for matched therapy of pediatric blood cancer patients: Dutch iTHER study experience
Dataset
EGAD00001015639
-
FASTQ files of the cell-free RNA from the maternal blood
Dataset
EGAD00001015416
-
AWI-GEN 2 Microbiome Dataset
Dataset
EGAD00001015449
-
Dataset for transcriptome and whole genome bisulfite sequencing of glioblastoma(GBM) tumor cells
Dataset
EGAD00001015614
-
AWI-GEN 2 Phenotype Dataset
Dataset
EGAD00001015440
-
DNA and RNAseq of serial biopsies from 75 DLBCL patients
Dataset
EGAD00001011816
-
RNA-seq data of Metabolic profiling of patient-derived organoids reveals nucleotide synthesis as a metabolic vulnerability in malignant rhabdoid tumors
Dataset
EGAD00001015391
-
Spatially resolved cellular and molecular drivers of cardiac remodelling in healthy and failing human hearts: Adult RNA (2025-07-31)
Dataset
EGAD00001015668
-
Genome and transcriptome sequence data from a malignant peripheral nerve sheath tumor patient
Dataset
EGAD00001015583
-
WTCCC case-control study for Coronary Artery Disease - Combined Controls
Study
EGAS00000000004
-
WTCCC case-control study for Type 1 Diabetes - Combined Controls
Study
EGAS00000000015
-
WTCCC case-control study for Coronary Artery Disease, Hypertension, T2D - combined cases
Study
EGAS00000000005
-
WGS_skin_punches
Study
EGAS00001004465
-
WTCCC case-control study for Type 2 Diabetes - Combined Controls
Study
EGAS00000000017
-
A new beta-globin mutation responsible of a beta-thalassemia (HbVar database ID 2928) was observed in 8 unrelated French families. The mutation carriers originated from Nord-Pas-de-Calais, a Northern French region where the chief town is Lille.5 unrelated mutation carriers were genotyped for a set of 12 microsatellites from chromosome 11, around the beta-globin gene. Among the 5 mutation carriers, 4 were genotyped for 97 European Ancestry Informative SNPs (EAIMs). 32 controls from Nord-Pas-de-Calais were genotyped for the microsatellites and SNPs.
Dac
EGAC00001000245
-
Cancer Genome Project Exome Sequencing
Dataset
EGAD00001000289
-
SC_DDD-G-3
Dataset
EGAD00010001602
-
ChIP-sequencing fragment coverage
Dataset
EGAD00010001671