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Ancestry and somatic profile predict acral melanoma origin and prognosis – WXS
Dataset
EGAD00001015755
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Ancestry and somatic profile predict acral melanoma origin and prognosis – RNA
Dataset
EGAD00001015756
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Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
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BIOCLOCK Phenotype Information Dataset
Dataset
EGAD00001015799
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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
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Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
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ecDNA copy number heterogeneity
Study
EGAS50000000509
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Clonal fitness inferred from timeseries modeling of single cell cancer genomes
Study
EGAS00001004448
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H3Africa - Deciphering Developmental Disorders in Africa
Study
EGAS00001008319
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Comprehensive Genomic Characterization of Refractory Multiple Myeloma Reveals a Complex Mutational and Structural Landscape Associated with Drug Resistance (H067)
Study
EGAS00001004363
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GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes using low pass whole genome sequencing and high density SNP genotyping in 2,657 individuals.
Study
EGAS00001001459
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Methylation sequencing of CSF-derived cell free DNA
Study
EGAS50000001365
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Northern Ireland COhort for the Longitudinal study of Ageing
Study
EGAS00001007915
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Genomic evolution and natural history of myeloproliferative neoplasms on therapy - triple-negative-ET
Dataset
EGAD00001016066
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Genomic evolution and natural history of myeloproliferative neoplasms on therapy - MPN_bulk
Dataset
EGAD00001016067
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Genomic evolution and natural history of myeloproliferative neoplasms on therapy - SCC_CALRmutated ET
Dataset
EGAD00001016068
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Mapping genetic variants underlying gene regulation in intestinal cell types to identify novel IBD drug targets
Dataset
EGAD00001016069
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The_Little_Princess_Knowledge_Bank_
Study
EGAS00001004237
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Genetic regulation of gene expression in human brain cell types
Study
EGAS00001006345
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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
-
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
-
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
-
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
-
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
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
-
cell-free DNA Target sequencing from primary and recurrent/metastatic breast cancer patients
Study
JGAS000812
-
Whole-genome sequencing of the parental tumor and established organoids from a patient with gastric-type cervical adenocarcinoma
Study
JGAS000796
-
Smoking-dependent expression alterations in nasal epithelium reveal immune impairment linked to germline variation and lung cancer risk.
Dac
EGAC50000000169