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Whole Genome Sequencing of HCC
Dataset
EGAD00001003994
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Clinical and genetic analysis of a rare syndrome associated with neoteny
Dataset
EGAD00001003593
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EGFR Mutant SCLC transformed exome seq
Dataset
EGAD00001001436
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Discovery of resistance mechanisms to the BRAF inhibitor vemurafenib in metastatic BRAF mutant melanoma
Dataset
EGAD00001000707
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Combination therapies for personalized cancer medicine
Dataset
EGAD00001000869
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Subclonal diversification of primary breast cancer
Dataset
EGAD00001000898
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ICGC Prostate Cancer Whole Genome Sequencing
Dataset
EGAD00001000891
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Breast Cancer FRT RNA seq
Dataset
EGAD00001000338
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Somatic mutations, clonal architecture and genomic evolution in multiple myeloma
Dataset
EGAD00001000339
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Identification of the underlying causal variant in a multi-generational family with autosomal dominant common variable immunodeficiency
Dataset
EGAD00001000363
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A common single nucleotide variant in T is strongly associated with chordoma
Dataset
EGAD00001000226
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Genetic mechanisms of resistance to chemotherapy in breast cancer
Dataset
EGAD00001000264
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Unraveling the genetic basis of a collagen migration defect in patients with a combined platelet dysfunction and reduced bone density
Dataset
EGAD00001000109
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Genetic landscape of hepatocellular carcinoma
Dataset
EGAD00001000131
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Whole Genome Sequencing accompanying Genetic landscape of pediatric Rhabdomyosarcoma
Dataset
EGAD00001000164
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PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Dataset
EGAD00001000017
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Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP)
Dataset
EGAD00001000026
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Genetic variation in Kuusamo
Dataset
EGAD00001000055
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Molecular characterization of invasive lobular carcinoma
Dataset
EGAD00001000288
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RNA sequencing
Dataset
EGAD00001000285
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Whole genome analyses of the childhood cancer neuroblastoma
Dataset
EGAD00001000282
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Screening for human epigenetic variation at CpG islands
Dataset
EGAD00001000059
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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
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Presence of rare potential pathogenic variants in subjects under 65 years old with very severe or fatal COVID‑19
Study
EGAS00001006372
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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
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A catalog of the genetic causes of Hereditary Angioedema in the Canary Islands (Spain)
Study
EGAS00001006547
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H3Africa - Kidney Disease Research Network
Study
EGAS00001006558
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Multi-organ landscape of therapy-resistant melanoma
Study
EGAS00001006644
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H3Africa - Genomic Characterization and Surveillance of Microbial Threats in West Africa
Study
EGAS00001007250
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H3Africa - Stroke Investigative Research and Education Networks
Study
EGAS00001007331
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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
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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