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Providing access to COVID-19 data: one year later
Blog
providing-access-to-covid-19
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The last addition to the list of clonal evolution studies in the EGA
Blog
the-last-addition-to-the-list-of-clonal-evolution-studies-in-the-ega
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The Federated EGA network
Blog
the-federated-ega-network
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Data upcycling, powered by EGA
Blog
data-upcycling-powered-by-ega
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Youth-GEMs, the project using data to define the mental health trajectories of young people
Blog
youth-gems-mental-health
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From research to data sharing: exploring EGA user's experiences
Blog
from-research-to-data-sharing
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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
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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
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Identification of gene mutations and fusion genes in patients with Sézary Syndrome
Study
EGAS00001001706
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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
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SNP array data for the Milieu Intérieur cohort
Study
EGAS00001002460
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MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma
Study
EGAS00001002608
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H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
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Mapping genetic variants that underlie gene regulation in intestinal cell types to identify novel, validated, Crohn’s disease drug targets
Study
EGAS00001003647
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Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Study
EGAS00001003931
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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
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The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH
Study
EGAS00001004285
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Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001004407
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Genome-wide associations of human gut microbiota variation and implications for causal inference analyses
Study
EGAS00001004420
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Deep genetic affinity between coastal Pacific and Amazonian natives evidenced by Australasian ancestry
Study
EGAS00001005022
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A rare CTSC mutation in Papillon-Lefèvre Syndrome
Study
EGAS00001005040
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Genome-wide data from Agta hunter-gatherers in Philippines
Study
EGAS00001005315
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Genome-wide Rare Variant Score Associates With Morphological Subtypes of Autism Spectrum Disorder
Study
EGAS00001005753
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Genome-wide genotype data for 1,433 ni-Vanuatu
Study
EGAS00001005910
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Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature
Study
EGAS00001006115