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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
-
Solve-RD multi-omics data chud-faivre cohort
Dataset
EGAD00001015811
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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
-
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
-
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
-
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
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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
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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
-
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