Genomics and Bioinformatics Shared Resource The Genomics and Bioinformatics Shared Resource (GBSR) was created in 2013 by the merging of the Microarray and DNA Sequencing Shared Resources in recognition of the dramatic changes in high-throughput DNA sequencing technologies in the past five years. Kelly A Frazer, PhD was appointed as Director of the new GBSR. Dr. Frazer is an established and highly productive investigator, who has broad expertise in the field of genomics. Additionally, Trey Ideker, PhD, a highly accomplished scientist in the field of Network Analysis, was appointed as co-Director. Under the new leadership, the reconfigured Shared Resource now includes a Bioinformatics Unit, whose services are deemed integral to the performance and analyses and interpretation of the various genomic assays. The current GBSR is a confederation of three units, the Biogem facility under the leadership of Kristen Jepsen, PhD, the VA Microarray and NGS facility under Nicholas Webster, PhD, and a Bioinformatics unit under Olivier Harismendy, PhD. The major objectives of the Genomics and Bioinformatics Shared Resource are to provide Cancer Center investigators with high quality standard, cutting-edge, and custom genomics services and data analyses, as well as consultation on experimental design and training/education about genomic methods and bioinformatics. The specific goals of the GBSR are as follows: 1. To provide expert consultation to MCC membership on experimental designs and analysis approaches of large-scale microarray and NGS datasets. 2. To generate high-throughput sequence data on Next Generation platforms in a cost-effective manner and offer this as a service for the MCC membership. 3. To develop pipelines for performing intermediate analysis of high-throughput sequence data including, DNA variant calling, mRNA isoform calling, miRNA analysis and DNA methylation analysis. 4. To establish the Infrastructure for advanced data analysis including, tumor profiling for DNA somatic mutations, differential expression analysis, as well as network and systems analysis.

Public Health Relevance

The availability of the Genomics and Bioinformatics Shared Resource enables our researchers to identify signal transduction pathways involved in carcinogenesis, new targets for therapeutic intervention, and biomarkers for cancer detection, prognosis, and treatment decision-making.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA023100-28
Application #
8934944
Study Section
Subcommittee G - Education (NCI)
Program Officer
Shafik, Hasnaa
Project Start
2014-07-21
Project End
2019-04-30
Budget Start
2014-07-21
Budget End
2015-04-30
Support Year
28
Fiscal Year
2014
Total Cost
$447,838
Indirect Cost
$156,033
Name
University of California San Diego
Department
Type
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Jiang, Qingfei; Jamieson, Catriona (2018) BET'ing on Dual JAK/BET Inhibition as a Therapeutic Strategy for Myeloproliferative Neoplasms. Cancer Cell 33:3-5
Ramirez, Oscar; Aristizabal, Paula; Zaidi, Alia et al. (2018) Implementing a Childhood Cancer Outcomes Surveillance System Within a Population-Based Cancer Registry. J Glob Oncol :1-11
Liu, Liang; Yang, Lin; Yan, Wei et al. (2018) Chemotherapy Induces Breast Cancer Stemness in Association with Dysregulated Monocytosis. Clin Cancer Res 24:2370-2382
Lwin, Thinzar M; Murakami, Takashi; Miyake, Kentaro et al. (2018) Tumor-Specific Labeling of Pancreatic Cancer Using a Humanized Anti-CEA Antibody Conjugated to a Near-Infrared Fluorophore. Ann Surg Oncol 25:1079-1085
Singh, Siddharth; Loomba, Rohit (2018) Role of two-dimensional shear wave elastography in the assessment of chronic liver diseases. Hepatology 67:13-15
Hartman, Sheri J; Nelson, Sandahl H; Myers, Emily et al. (2018) Randomized controlled trial of increasing physical activity on objectively measured and self-reported cognitive functioning among breast cancer survivors: The memory & motion study. Cancer 124:192-202
Hoffmann, Hanne M; Gong, Ping; Tamrazian, Anika et al. (2018) Transcriptional interaction between cFOS and the homeodomain-binding transcription factor VAX1 on the GnRH promoter controls Gnrh1 expression levels in a GnRH neuron maturation specific manner. Mol Cell Endocrinol 461:143-154
Liu, Xuxiang; Cao, Minghui; Palomares, Melanie et al. (2018) Metastatic breast cancer cells overexpress and secrete miR-218 to regulate type I collagen deposition by osteoblasts. Breast Cancer Res 20:127
Huang, Justin K; Carlin, Daniel E; Yu, Michael Ku et al. (2018) Systematic Evaluation of Molecular Networks for Discovery of Disease Genes. Cell Syst 6:484-495.e5
Kalyanaraman, Hema; Schwaerzer, Gerburg; Ramdani, Ghania et al. (2018) Protein Kinase G Activation Reverses Oxidative Stress and Restores Osteoblast Function and Bone Formation in Male Mice With Type 1 Diabetes. Diabetes 67:607-623

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