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Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation
Study
EGAS00001001575
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A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
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The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
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Long-term organoid culture of a small intestinal neuroendocrine tumor
Study
EGAS00001007093
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UK10K NEURO FSZ
Study
EGAS00001000118
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Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
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Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_
Study
EGAS00001000490
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Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002
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Genome_Diversity_in_Africa_Project__Benin
Study
EGAS00001001688
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Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
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Whole-genome Sequencing Suggests Mechanisms for 22q11.2 deletion-associated Parkinson’s disease
Study
EGAS00001002275
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Pediatric Whole Genome Sequencing Diagnostic Utility
Study
EGAS00001001623
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Family-based GWAS for CRSwNP
Study
EGAS00001002665
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GoDARTS T2D-GENES Exome Sequencing Study is a subset of the ~52,000 Type 2 diabetes exome sequencing project.
Study
EGAS00001002937
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Botswana 15 autosomal unlinked microsatellites
Study
EGAS00001002380
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Biological insights from the whole genome sequences of human embryonic stem cell lines
Study
EGAS00001002400
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Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
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EXOME-WIDE ASSOCIATION ANALYSIS OF CORONARY ARTERY DISEASE IN THE KINGDOM OF SAUDI ARABIA POPULATION
Study
EGAS00001001645
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High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform, P49-P104 and run1 replicates
Study
EGAS00001006595
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33 patients with Monoclonal Gammopathy of Undetermined Significance (MGUS) had whole exome sequencing performed. Cells were sorted by FACSAria using CD138, CD19 and CD56 to obtain a pure abnormal plasma cell population. Generated somatic variants were compared to a previous study of 463 multiple myeloma patients.
Study
EGAS00001001658
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Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
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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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Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Study
EGAS00001002052
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Genomic and Epigenomic Features of Primary and Recurrent Hepatocellular Carcinomas
Study
EGAS00001002094
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Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102