The ?UCSC-Buck Genome Data Analysis Center for the Genomic Data Analysis Network? will develop state-of-the-art methods for integrating various types of data to discover the genetic pathways, the microenvironment, the originating cells, and the oncogenic processes driving the initiation and progression of tumors. The long term goals of the project are to identify highly accurate models detailing the faulty genetic circuitry at work in each subclone of a patient?s tumor, as well as any ?normal? cells acting as accomplices by supporting the cancer microenvironment. The ultimate objective is to encode computer algorithms that can search a patient?s individual pathway diagram for the best combination of interventions to eliminate every tumor cell, while preserving the health of every normal cell, in their body. Integrative pathway analysis methods will be developed to reveal signatures of tumor subtypes from Pan-Cancer and external datasets. New technologies will be established for uncovering network models tailored to individual patients. The tools will be deployed as part of an active collaboration to support the specific projects of the Genome Data Analysis Network. Novel probabilistic graphical models will be used to infer disrupted signaling. Cellular signatures will be collected from the analysis of normal cells, cancer cell line models, and Pan-Cancer investigations. Novel machine-learning methods, guided by pathway mechanisms, will be established to identify cell state signatures in heterogeneous patient samples. This work will reveal rare mutations driving metastatic transformation that are currently of unknown significance. New clues about the genetic circuitry promoting response and resistance to treatment will be established. Finally, cross-tumor connections that relate tumors of one type to a different type will suggest new avenues for treatment.
Computational strategies for interpreting the results of cancer genome sequencing projects are in desperate need. To select appropriate treatment strategies for a patient, an accurate model of the altered genetic wiring in the tumor is needed as well as how that wiring relates to other tumors and to other normal cells at various stages of differentiation. The research will establish resources and software to contribute such methodologies for the Genome Data Analysis Network projects that will subsequently be released into the public domain to benefit the entire scientific community.
Sendorek, Dorota H; Caloian, Cristian; Ellrott, Kyle et al. (2018) Germline contamination and leakage in whole genome somatic single nucleotide variant detection. BMC Bioinformatics 19:28 |
Taylor, Alison M; Shih, Juliann; Ha, Gavin et al. (2018) Genomic and Functional Approaches to Understanding Cancer Aneuploidy. Cancer Cell 33:676-689.e3 |
Saltz, Joel; Gupta, Rajarsi; Hou, Le et al. (2018) Spatial Organization and Molecular Correlation of Tumor-Infiltrating Lymphocytes Using Deep Learning on Pathology Images. Cell Rep 23:181-193.e7 |
Malta, Tathiane M; Sokolov, Artem; Gentles, Andrew J et al. (2018) Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation. Cell 173:338-354.e15 |
Ellrott, Kyle; Bailey, Matthew H; Saksena, Gordon et al. (2018) Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines. Cell Syst 6:271-281.e7 |
Campbell, Joshua D; Yau, Christina; Bowlby, Reanne et al. (2018) Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas. Cell Rep 23:194-212.e6 |
Gao, Qingsong; Liang, Wen-Wei; Foltz, Steven M et al. (2018) Driver Fusions and Their Implications in the Development and Treatment of Human Cancers. Cell Rep 23:227-238.e3 |
Thorsson, Vésteinn; Gibbs, David L; Brown, Scott D et al. (2018) The Immune Landscape of Cancer. Immunity 48:812-830.e14 |
Radovich, Milan; Pickering, Curtis R; Felau, Ina et al. (2018) The Integrated Genomic Landscape of Thymic Epithelial Tumors. Cancer Cell 33:244-258.e10 |
Berger, Ashton C; Korkut, Anil; Kanchi, Rupa S et al. (2018) A Comprehensive Pan-Cancer Molecular Study of Gynecologic and Breast Cancers. Cancer Cell 33:690-705.e9 |
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