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Showing 1 to 9 of 9 for “"pan-cancer analysis"”.

  1. Pan-Cancer Analysis of Non-Coding Driver Mutations

    Cancers are caused by genomic alterations known as drivers. As drivers have broad applications in precision oncology, their discovery has become one of the central motivations for cancer genomics. At present, the majority of drivers have been found in the ~2% protein-coding regions. Despite an …

    toronto-retro Repository record for Pan-Cancer Analysis of Non-Coding Driver Mutations (opens in a new tab)

  2. Pan-Cancer Analysis of RNA Dysregulation, Somatic Mutations, and Matrix Stiffness using Bioinformatics Approaches

    Cancer is a complex disease driven by genetic mutations, epigenetic modifications, and alterations in the tumor microenvironment. Understanding these intricate molecular mechanisms is crucial for advancing cancer diagnosis, prognosis, and treatment. RNA sequencing (RNA-seq) has emerged as a …

    wustl Repository record for Pan-Cancer Analysis of RNA Dysregulation, Somatic Mutations, and Matrix Stiffness using Bioinformatics Approaches (opens in a new tab)

  3. Systems biology of deregulated splicing in cancer. A pan-cancer analysis of dysfunctional splicing machinery and alternative splicing events.

    … this project, we set out to perform a systematic analysis of aberrant splicing events in cancer cell lines from two perspectives: deregulated splicing because of dysfunctional splicing factors and the appearance of de novo splicing events because of splice-disruption mutations in the DNA sequence. …

    chalmers Repository record for Systems biology of deregulated splicing in cancer. A pan-cancer analysis of dysfunctional splicing machinery and alternative splicing events. (opens in a new tab)

  4. Investigation of Genetic Alterations In Emt Suppressor, Dear1, Through Pan-Cancer Analysis and Ultra-Deep Targeted Sequencing In Ductal Carcinoma In Situ

    … predictive and prognostic biomarkers for breast cancers with a heightened risk of progression from DCIS to IDC. Our laboratory has previously discovered a novel TRIM family member, <em>DEAR1</em> (<em>Ductal Epithelium Associated Ring Chromosome 1, annotated as TRIM62)</em> within chromosome …

    uthsc Repository record for Investigation of Genetic Alterations In Emt Suppressor, Dear1, Through Pan-Cancer Analysis and Ultra-Deep Targeted Sequencing In Ductal Carcinoma In Situ (opens in a new tab)

  5. TimiGP: A Computational Framework to Determine the Tumor Immune Microenvironment Associated with Prognosis and Immunotherapy Response

    … microenvironment (TIME) drastically impacts cancer patients’ clinical outcomes, including prognosis and immunotherapy response. However, understanding TIME remains challenging due to its complexity and heterogeneity. In this dissertation, we introduce TimiGP (Tumor Immune Microenvironment …

    uthsc Repository record for TimiGP: A Computational Framework to Determine the Tumor Immune Microenvironment Associated with Prognosis and Immunotherapy Response (opens in a new tab)

  6. The Intra-Tumour Heterogeneity Landscape of Human Cancers

    … a selective advantage and can induce clonal expansions. Incomplete clonal expansions give rise to intra-tumour heterogeneity. Somatic mutations can be measured through massively parallel sequencing, where mutations that are supporting incomplete expansions will appear as subclonal. These …

    cambridge Repository record for The Intra-Tumour Heterogeneity Landscape of Human Cancers (opens in a new tab)

  7. Patterns of somatic genome rearrangement in human cancer

    Cancer development is driven by somatic genome alterations, ranging from single point mutations to larger structural variants (SV) affecting kilobases to megabases of one or more chromosomes. Studies of somatic rearrangement have previously been limited by a paucity of whole genome sequencing data, …

    cambridge Repository record for Patterns of somatic genome rearrangement in human cancer (opens in a new tab)

  8. Integrative network modeling of large multidimensional cancer datasets

    … containing measurements from thousands of cancer tumors. To harness the potential of the amassing data sets, we introduce new modeling techniques and generalise existing methods for large-scale integration of cancer data. These methods aim to construct network models that link genetic, …

    goteborg Repository record for Integrative network modeling of large multidimensional cancer datasets (opens in a new tab)

  9. Signatures of chromosomal instability in human cancers

    … molecular characteristics to be described in cancer. Since its detection by light microscopy in the late 19th century, technological advances have facilitated the observation of CIN at increasing resolution, revealing an extreme genomic complexity which we are only beginning to understand. As …

    cambridge Repository record for Signatures of chromosomal instability in human cancers (opens in a new tab)