-
Purified vs unpurified stem cell-islets
Dataset
EGAD50000001396
-
Tcells_CD_scRNAseq
Dataset
EGAD00010001649
-
Capture Hi-C on Hodgkin lymphoma
Dataset
EGAD00001004321
-
Sequencing data for ICGC Oesophageal Adenocarcinoma tissue samples - barretts_1
Dataset
EGAD00001001394
-
Thirty cutaneous SCC WES tumour samples with matched normal
Dataset
EGAD00001002253
-
eQTL summary statistics
Dataset
EGAD00001005041
-
Metagenome for FINRISK2002
Dataset
EGAD00001007035
-
10x genomics RNAseq of an isogenic human iPSC model of SMA
Dataset
EGAD00001011259
-
eMERGE Network Genome-Wide Association Study of Red Cell Indices, White Blood Count (WBC) Differential, Diabetic Retinopathy, Height, Serum Lipid Levels, Specifically Total Cholesterol, HDL (High Density Lipoprotein), LDL (Low Density Lipoprotein), and Triglycerides, and Autoimmune Hypothyroidism.
Study
phs000360
-
Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis
Study
EGAS00001000515
-
Use_of_Deep_Sequencing_to_Dectect_Clonal_Mutations_In_Sun_Exposed_Skin_Epidermis_PART2
Study
EGAS00001000603
-
Raw multi-omics dataset from the lungNENomics cohort of lung neuroendocrine tumours
Study
EGAS00001005979
-
National Cancer Institute (NCI) Adding Hispanics to Ongoing GWAS in Colorectal Cancer
Study
phs001193
-
Gabriella Miller Kids First Pediatric Research Program in Germline and Somatic Variants in Myeloid Malignancies in Children
Study
phs002187
-
Single-cell CITE-seq and TCR-seq data from AIM⁺ HIV-1-specific T cells
Dataset
EGAD50000002247
-
Head and Neck Organoid Biobank cohort, Issing et. al., 2025, RNA + WES data
Dataset
EGAD50000001733
-
Single-cell characterization of human GBM reveals regional differences in tumor-infiltrating leukocyte activation
Dataset
EGAD50000000434
-
RNA-seq transcriptome of bronchial brush samples from COPD and control
Dataset
EGAD00001002003
-
Sequencing data for oesophageal / related samples - Kazachenka et al (DNA)
Dataset
EGAD00001011095
-
3/7 Psychiatric Genomics Consortium: Finding Actionable Variation
Study
phs003138
-
Ischemic Stroke Genetics Study (ISGS)
Study
phs000102
-
The Gene Partnership (TGP) - eMERGE Data
Study
phs000495
-
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Study
EGAS00001000055
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
Are children born after medical assisted reproduction at greater risk of having an increased de novo mutation rate?
Study
EGAS00001005569
-
Liquid Biopsy Versus Tissue Biopsy to Assess Acquired Resistance and Tumor Heterogeneity in Gastrointestinal Cancers
Study
phs001853
-
cfMeDIP-seq for 18 patients with pleural mesothelioma
Dataset
EGAD50000002126
-
ICGC PCAWG Dataset: MALY-DE_PCAWG_RNA-Seq_Star
Dataset
EGAD00001003560
-
ICGC PCAWG Dataset: MALY-DE_PCAWG_RNA-Seq_TopHat2
Dataset
EGAD00001003561
-
Genomic Evolution of Breast Cancer Metastasis and Relapse
Dataset
EGAD00001002698
-
Circulating Tumor Cell Heterogeneity in Neuroendocrine Prostate Cancer by Single Cell Copy Number Analysis
Study
phs002462
-
Next Generation Mendelian Genetics: Congenital Hyperinsulinism
Study
phs000539
-
The spectrum of somatic mutations in high-risk acute myeloid leukemia with -7/del(7q)
Study
phs000759
-
Kids First: Genomics of Orofacial Clefts in the Philippines
Study
phs002595
-
Health Information National Trends Survey-SEER (HINTS-SEER)
Study
phs004065
-
DHODH is a synthetic-lethal vulnerability in BCOR-deficient acute myeloid leukemia
Study
EGAS50000001060
-
MED12L Gene Alterations Define Aggressive BRCA2-Mutant Prostate Cancers
Study
EGAS00001001615
-
Drug screening and whole genome sequencing of primary cells and cell lines from ovarian cancer patients to associate genomic aberrations with in vitro drug sensitivities
Study
EGAS00001002239
-
DHODH is a synthetic-lethal vulnerability in BCOR-deficient acute myeloid leukemia
Study
EGAS50000001108
-
Comprehensive spatial landscape and plasticity of immunosuppressive fibroblasts in breast cancer
Study
EGAS50000000220
-
GOSH_Childhood_Leukemia_Behjati_WellcomeCore_RNA
Study
EGAS00001007616
-
WGS data from both single-cell and bulk samples
Dataset
EGAD50000002411
-
Sequence data for "An allele-resolved nanopore-guided tour of the human placental methylome" (Kindlova et al 2025)
Dataset
EGAD50000001850
-
WGS data from PASS-01 trial
Dataset
EGAD50000002309
-
WTS data from PASS-01 trial
Dataset
EGAD50000002308
-
Shallow whole genome sequencing DETECT samples
Dataset
EGAD50000001333
-
scKaryoSeq of CRISPR-Cas9 edited primary human T cells
Dataset
EGAD50000000929
-
RNA-seq dataset
Dataset
EGAD50000000347
-
Low-coverage Whole Genome Sequencing, Colorectal adenomas, NKI-AvL TGO series Stool-Proteomics
Dataset
EGAD00001004075
-
Bajau and Saluan adaptation study data
Dataset
EGAD00001004207