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BLUEPRINT release August 2016, Bisulfite-Seq for Chronic Lymphocytic Leukemia, on genome GRCh38
Dataset
EGAD00001002396
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Genome and transcriptome sequence data from a metastatic carcinoma of the lung patient
Dataset
EGAD00001002983
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Bam files from whole exome sequencing (WES)from multiple laser microdissected regions from tumor and paired biopsies from metastatic lesions.
Dataset
EGAD00001002772
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Genome and transcriptome sequence data from a metastatic adenocarcinoma of colon patient
Dataset
EGAD00001011015
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Targeted DNA sequencing on bulk bone marrow and peripheral blood
Dataset
EGAD00001011083
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Exome sequencing data from two small cell prostate cancer patients
Dataset
EGAD00001011149
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Intra-prostatic tumour evolution, steps in metastatic spread and histogenomic associations revealed by integration of multi-region whole genome sequencing with histopathological features
Dataset
EGAD00001011174
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MSC_busulfan_small_intestine_organoids
Dataset
EGAD00001011176
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FASTQ files of the cell-free RNA from the maternal blood
Dataset
EGAD00001015416
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AWI-GEN 2 Microbiome Dataset
Dataset
EGAD00001015449
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Dataset for transcriptome and whole genome bisulfite sequencing of glioblastoma(GBM) tumor cells
Dataset
EGAD00001015614
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AWI-GEN 2 Phenotype Dataset
Dataset
EGAD00001015440
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DNA and RNAseq of serial biopsies from 75 DLBCL patients
Dataset
EGAD00001011816
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BLUEPRINT release August 2016, Bisulfite-Seq for Multiple Myeloma, on genome GRCh38
Dataset
EGAD00001002521
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Genome and transcriptome sequence data from an adenocarcinoma of unknown primary cancer patient
Dataset
EGAD00001002606
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Genome and transcriptome sequence data from a metastatic gastric cancer patient
Dataset
EGAD00001004904
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Genotype data
Dataset
EGAD00001005038
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NIHR BioResource Rare Diseases WGS project - Ehler-Danlos (ED) and ED-like Syndromes (EDS) Rare Disease domain
Dataset
EGAD00001005123
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Cell type-specific transcriptomics of esophageal adenocarcinoma
Dataset
EGAD00001005508
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Genome and transcriptome sequence data from a metastatic pancreatic neuroendocrine patient
Dataset
EGAD00001005763
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Ovarian cancer sample size analysis
Dataset
EGAD00001005947
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Whole Genome Sequencing of Human Organoid Lines (2020-02-20)
Dataset
EGAD00001005995
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Next Generation Sequencing Characterization of Tregs in Human Peripheral Blood during Autoimmunity
Dataset
EGAD00001006193
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Somatic mutations reveal embryonic genetic bottlenecks generating placental mosaicism
Dataset
EGAD00001006337
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Whole Exome Sequencing of High grade T1 non-muscle invasive bladder cancer
Dataset
EGAD00001006346
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scRNA-seq raw data
Dataset
EGAD00001006436
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PCCRC versus prevalent CRC
Dataset
EGAD00001006987
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The evolution of hematopoietic cells under cancer therapy
Dataset
EGAD00001007706
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RNA-seq data of Metabolic profiling of patient-derived organoids reveals nucleotide synthesis as a metabolic vulnerability in malignant rhabdoid tumors
Dataset
EGAD00001015391
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Genome and transcriptome sequence data from a non-small cell lung carcinoma patient
Dataset
EGAD00001010942
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Genome and transcriptome sequence data from a metastatic breast ductal carcinoma patient
Dataset
EGAD00001011021
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Chromatin accessibility (ATAC-seq) of human acute leukemias and healthy donors
Dataset
EGAD00001011050
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47 urothelial cancer patients WES and 38 RNAseq
Dataset
EGAD00001011063
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Organoid Derivation Project - GRCh38 - RNAseq (2023-06-22)
Dataset
EGAD00001011092
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ATAC-seq and RNA-seq datasets of CD14+ monocytes from healthy donors
Dataset
EGAD00001011113
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WXS Normal Samples Javelin head and neck 100
Dataset
EGAD00001011321
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Spatially resolved cellular and molecular drivers of cardiac remodelling in healthy and failing human hearts: Adult RNA (2025-07-31)
Dataset
EGAD00001015668
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Genome and transcriptome sequence data from a malignant peripheral nerve sheath tumor patient
Dataset
EGAD00001015583
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FEGA and European GDI: working together to improve human health
Blog
fega-and-gdi
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WTCCC case-control study for Coronary Artery Disease - Combined Controls
Study
EGAS00000000004
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WTCCC case-control study for Type 1 Diabetes - Combined Controls
Study
EGAS00000000015
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WTCCC case-control study for Coronary Artery Disease, Hypertension, T2D - combined cases
Study
EGAS00000000005
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WGS_skin_punches
Study
EGAS00001004465
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WTCCC case-control study for Type 2 Diabetes - Combined Controls
Study
EGAS00000000017
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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