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Phosphoproteomics adds value to treatment recommendations in molecular tumor boards
Study
EGAS00001007891
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The University of Hong Kong Intestinal Metaplasia Organoids Study
Study
EGAS00001007899
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Northern Ireland COhort for the Longitudinal study of Ageing
Study
EGAS00001007915
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Transcriptomics-driven classification of ALAL
Study
EGAS00001007967
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Single-cell atlas of > 1.5 million PBMC with multi-layer omics data in Japanese
Study
EGAS00001008016
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Patient-derived tumoroids from CIC::DUX4 rearranged sarcoma identify MCL1 as a therapeutic target
Study
EGAS00001008039
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Genetic origins of the Kiritimati population from central-eastern Micronesia
Study
EGAS00001008060
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Epi2Diag
Study
EGAS00001008070
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Dataset with genome-wide array data from Algerian Amazigh (Chaoui and Mozabite) and non-Amazigh individuals
Study
EGAS00001007235
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Single cell TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008161
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OMKar
Study
EGAS00001008245
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Peruvian Population Genomics: Unraveling the Genetic Landscape and Admixture Dynamics of Urban Populations
Study
EGAS00001008264
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H3Africa - Deciphering Developmental Disorders in Africa
Study
EGAS00001008319
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Genome-wide methylation detection and episignature analysis using PacBio long-read sequencing
Study
EGAS00001008250
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MorphoITH: A Framework for Deconvolving Intra-Tumor Heterogeneity Using Tissue Morphology
Study
EGAS50000001064
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Osteosarcoma 3D patient derived cultures to test genome-informed personalized treatment options; a feasibility study
Study
EGAS50000001583
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Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Study
EGAS00001002606
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Whole-exome variant calling of individuals from the study of sepsis and acute distress respiratory syndrome in Spain
Study
EGAS50000001119
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Plasma pQTLs in INTERVAL cohort
Study
EGAS00001002555
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Multi-omic analysis of Down Syndrome in thyroid
Study
EGAS00001007677
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Ultra-long sequencing for contiguous haplotype resolution of the human immunoglobulin heavy chain locus
Study
EGAS50000001042
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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
-
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
-
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
-
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
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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
-
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
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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
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SMARCB1 loss activates patient-specific distal oncogenic enhancers in malignant rhabdoid tumors
Study
EGAS00001007590