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An MTOR mutation hitchhikes through renal embryogenesis, driving multifocal, multiphenotypic tumours - scRNA
Dataset
EGAD00001011647
-
Using genetics to identify cell types and mechanisms underlying susceptibility to primary sclerosing cholangitis
Dataset
EGAD00001011815
-
Single-Cell DNA Methylation Profiling via scTAMseq
Dataset
EGAD00001015498
-
A spatiotemporal cancer cell trajectory underlies glioblastoma heterogeneity
Dataset
EGAD00001015516
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Genetic architecture of male infertility in India
Dataset
EGAD00001015606
-
PacBio Rare Disease Study
Dataset
EGAD00001015611
-
Embryonic tumour transmission in monozygotic twins
Dataset
EGAD00001015681
-
Genomic and Functional Profiling of Acral Melanoma from the admixed Brazilian Population Reveals Disease Drivers and Targetable Vulnerabilities
Dataset
EGAD00001015690
-
Insights into non-crossover recombination from long-read sperm sequencing
Dataset
EGAD00001015736
-
Understanding the development of resident memory T cells (Trm) in the human small intestine using integrative multiomic approaches: Adult RNA (2025-10-14)
Dataset
EGAD00001015739
-
DNMT3A-R882 mutations intrinsically drive dysfunctional neutropoiesis from human haematopoietic stem cells
Dataset
EGAD00001015750
-
A next-generation dual guide CRISPR system for genetic interaction library screening
Dataset
EGAD00001015754
-
Ancestry and somatic profile predict acral melanoma origin and prognosis – WXS
Dataset
EGAD00001015755
-
Ancestry and somatic profile predict acral melanoma origin and prognosis – RNA
Dataset
EGAD00001015756
-
Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
-
BIOCLOCK Phenotype Information Dataset
Dataset
EGAD00001015799
-
Solve-RD multi-omics data chud-faivre cohort
Dataset
EGAD00001015811
-
On-target mutations confer resistance to WRN helicase inhibitors in Microsatellite Unstable Cancer Cells
Dataset
EGAD00001015822
-
Whole-Genome Sequences from five human populations of Sudan
Dataset
EGAD00001015636
-
Mapping Cells and Interactions in the Thymus Across Development and Aging (2025-07-28)
Dataset
EGAD00001015660
-
WGS dataset of Hepatoblastoma tumoroid biobank as a key resource for tumour genetics
Dataset
EGAD00001015671
-
Integrated single cell analysis identifies CD39+ tumor-associated NK cells with cytotoxic potential in NSCLC
Dataset
EGAD50000001695
-
Mapping genetic variants underlying gene regulation in intestinal cell types to identify novel IBD drug targets
Dataset
EGAD00001016069
-
Genomic evolution and natural history of myeloproliferative neoplasms on therapy - triple-negative-ET
Dataset
EGAD00001016066
-
Genomic evolution and natural history of myeloproliferative neoplasms on therapy - MPN_bulk
Dataset
EGAD00001016067
-
Genomic evolution and natural history of myeloproliferative neoplasms on therapy - SCC_CALRmutated ET
Dataset
EGAD00001016068
-
Epigenetic characterization of patient-derived glioblastoma stem cell (GSC)
Dataset
EGAD50000002603
-
Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - WGS data
Study
EGAS50000000657
-
Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - MEGA chip data
Study
EGAS50000000658
-
Breast_Cancer_Somatic_Genetics_Study_
Study
EGAS00001000195
-
Multimodal epigenetic sequencing analysis of cell-free DNA identifies biomarkers for ALS diagnosis and progression
Study
EGAS50000001267
-
The Genetic History of Greenlandic-European contact
Study
EGAS00001004933
-
Detection of clinically relevant genetic and transcriptomic landscape in DLBCL uniformly treated by R-CHOP
Study
EGAS00001002657
-
Malignant mesothelioma EWAS on European prospective study
Study
EGAS00001006432
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Study
EGAS00001000416
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator
Study
EGAS00001000417
-
Identification of gene mutations and fusion genes in patients with Sézary Syndrome
Study
EGAS00001001706
-
Prognostic relevance of microenvironmental factors CD163 and CD8 combined with EZH2 and chromosome 18 gain in a validation cohort of follicular lymphoma patients of the Lunenburg Lymphoma Biomarker Consortium
Study
EGAS00001002049
-
SNP array data for the Milieu Intérieur cohort
Study
EGAS00001002460
-
Lindsey E. Jones et al. Patient-derived cells from recurrent tumors that model the evolution of IDH-mutant glioma. Neuro-Oncology Advances, 2020. We established robust, versatile, and well-characterized Patient Derived Cells (PDC) of an IDH1-mutant astrocytoma and an IDH1-mutant oligodendroglioma that represents defined evolutionary stages of chemotherapy-induced hypermutation. The PDCs retain tumor subtype defining features over time as well as classic hallmarks of cancer, including anchorage independent growth and cell immortality. The integrated phylogenies composed of PDCs,single-cell-derived PDCs, patient-derived xenografts, and corresponding spatiotemporal tumor tissue samples also provide new insight into the clonality, evolutionary pattern, and immense mutational load of hypermutated IDH mutant gliomas.
Study
EGAS00001003992
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma
Study
EGAS00001002608
-
H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
-
Mapping genetic variants that underlie gene regulation in intestinal cell types to identify novel, validated, Crohn’s disease drug targets
Study
EGAS00001003647
-
Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Study
EGAS00001003931
-
The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH
Study
EGAS00001004285
-
Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001004407
-
Genome-wide associations of human gut microbiota variation and implications for causal inference analyses
Study
EGAS00001004420
-
Deep genetic affinity between coastal Pacific and Amazonian natives evidenced by Australasian ancestry
Study
EGAS00001005022
-
A rare CTSC mutation in Papillon-Lefèvre Syndrome
Study
EGAS00001005040
-
Genome-wide data from Agta hunter-gatherers in Philippines
Study
EGAS00001005315
-
Genome-wide Rare Variant Score Associates With Morphological Subtypes of Autism Spectrum Disorder
Study
EGAS00001005753
-
Genome-wide genotype data for 1,433 ni-Vanuatu
Study
EGAS00001005910
-
Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature
Study
EGAS00001006115
-
Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID‑19
Study
EGAS00001006372
-
Bulk-tissue RNA-sequencing paired nuclear and cytoplasmic fractions of anterior prefrontal cortex, cerebellar cortex and putamen tissues from post-mortem neuropathologically-confirmed control individuals.
Study
EGAS00001006380
-
A catalog of the genetic causes of Hereditary Angioedema in the Canary Islands (Spain)
Study
EGAS00001006547
-
H3Africa - Kidney Disease Research Network
Study
EGAS00001006558
-
Multi-organ landscape of therapy-resistant melanoma
Study
EGAS00001006644
-
H3Africa - Genomic Characterization and Surveillance of Microbial Threats in West Africa
Study
EGAS00001007250
-
H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
-
Genome-wide DNA methylation sequencing identifies epigenetic perturbations in the upper airways under long-term exposure to moderate levels of ambient air pollution
Study
EGAS00001007374
-
RNA sequencing in primary inflammatory (TPP) macrophages following deletion of a disease-associated gene desert at chr21q22, disruption of ETS2, or treatment of ETS2-edited macrophages with a HIF1α stabiliser.
Study
EGAS00001007553
-
SMARCB1 loss activates patient-specific distal oncogenic enhancers in malignant rhabdoid tumors
Study
EGAS00001007590
-
Genome-wide association study identifies common variants associated with breast cancer in South African Black women
Study
EGAS00001008032
-
Array-based DNA methylation analysis in blood from patients with Snijders Blok–Campeau syndrome (CHD3)
Study
EGAS00001008414
-
Cell-free DNA methylation profiling for non-invasive detection and classification of lymphoma
Study
EGAS50000001463
-
Huch Lab, Max Planck Institute of Molecular Cell Biology and Genetics
Dac
EGAC50000000112
-
The Agotes, a genetic isolate within the Basque genetic landscape
Study
EGAS00001008390