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Genomic Profiling of Pediatric Tumors by Cell Free DNA Sequencing
Study
EGAS50000000072
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Integrative analysis reveals a macrophage-predominant, immunosuppressive immune microenvironment and subtype-specific therapeutic vulnerabilities in advanced salivary gland cancer
Study
EGAS50000000809
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A prospective study identifies MisMatch Repair genes as candidate predisposing genes for uveal melanoma.
Study
EGAS50000000914
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Emirati Genome Project subset of 43,608 WGS samples for population-scale variant discovery and allele frequency mapping.
Study
EGAS50000001071
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Single-Gene vs. Panel Sequencing in Advanced HR+/HER2− Breast Cancer
Study
EGAS00001008200
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CDK4/6 inhibition in advanced chordoma: final results of the NCT PMO-1601
Study
EGAS00001007985
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A circulating biomarker for severity of facioscapulohumeral muscular dystrophy
Study
EGAS00001007350
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First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
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Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
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mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
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In this study, blood-brain barrier (BBB)-forming brain endothelial-like cells were generated from apolipoprotein E gene allele E4 (APOE4, high AD risk) and allele E3 (APOE3, lower AD risk) carrying patient-derived induced pluripotent stem cells (iPSCs). Cells were subsequently exposed to focused ultrasound and microbubbles (FUS+MB) to induce BBB opening and their transcriptome analysed. RNA sequencing (RNA-seq) results demonstrated minimal changes in the gene expression following FUS+MB suggesting safety of FUS+MB application in the clinical setting.
Study
EGAS00001005944
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Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
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High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform
Study
EGAS00001006103
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Local In Time Statistics for processual research
Study
EGAS00001002520
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RNAseq data to study PRPF6 regulated splice forms in colon cancer cell lines
Study
EGAS00001000761
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Assessing the impact of low frequency coding variants on disease risk using the Exomechip
Study
EGAS00001000584
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Whole Genome Sequencing of Asian Lung Cancers: Second Hand Smoke is Not Responsible for Higher Incidence of Lung Cancer Among Asian Never-Smokers
Study
EGAS00001000621
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Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Study
EGAS00001003564
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McGill Epigenomics Mapping Centre
Study
EGAS00001000995
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Polymorphisms in the mitochondrial genome are associated with bullous pemphigoid in Germans
Study
EGAS00001003932
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UK10K COHORT ALSPAC
Study
EGAS00001000090
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Genetic_Heterogeneity_of_the_familial_gastric_neuroendocrine_tumors
Study
EGAS00001002273
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Genome_Diversity_in_Africa_Project__Uganda
Study
EGAS00001002523
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Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
Study
EGAS00001000737
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Dynamics of multiple resistance mechanisms in plasma DNA and their clinical implications for NSCLC patients receiving EGFR-targeted therapies
Study
EGAS00001002908