- Genomics High-Throughput Facility (GHTF) A revolution has occurred in biomedicine in which genomics information is enabling faster and more accurate diagnoses and precise tailoring of therapeutics to patients. This revolution was triggered by developments in space age miniaturization of devices to enable high throughput, chemistries and spectroscopic advances for labeling, and use of computer technologies to advance chip-based products and parallel data processing and communications to enable personalized computing. This revolution is technology-driven. The first mission of the Genomics High Throughput Facility (GHTF) as a shared resource of the Chao Family Comprehensive Cancer Research Center (CFCCC) is to act as a conduit to introduce emerging genomics technologies so that they can be effectively accessed by the broadest spectrum of researchers. Investment in this shared resource by the CFCCC has been leveraged by nationally-funded instrument grants and campus cost-sharing. These investments have made Affymetrix microarrays, Illumina HiSeq next generation sequencing and PacBio third generation sequencing available to cancer researchers within one or two years of introduction to the workspace--long before they were commercially available for experimentally-tailored formats. These technologies enabled state-of-the-art research which has translated in a very short time into identification of unexpected roles for transcription factors, alternative splicing and polyadenylation by Cancer Center researchers. Introduction of the technologies at the campus level has the additional value of stimulating collaborations and feedback into further interdisciplinary development of these technologies. The second mission of the GHTF is to train a new generation of researchers in the analysis of genomics data. In the current funding period, DNA sequencing analysis pipelines for HiSeq and PacBio sequencing were established. A Bioinformatics Consulting Service was implemented to insure impact of these data on cancer research. Key future development priorities for CFCC researchers by the GHTF are: 1) development of a single-cell analysis platform and 2) expansion of bioinformatics training and analysis. Tumor populations are heterogeneous collections of cells and that to study them effectively requires the ability to discriminate among them. GHTF will introduce a microfluidic system for preparation of sequencing libraries from individual cells. The ability to analyze large streams of data is arguably now the limiting technology for application of genomics to cancer research. We made substantial progress in this area in the current funding period and now will expand these efforts with longer and more specialized workshops tailored to beginning and advanced applications, additional staff time for bioinformatics, and access to cancer-related pathway databases.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA062203-22
Application #
9632701
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-02-01
Budget End
2020-01-31
Support Year
22
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Type
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92617
Koay, Eugene J; Lee, Yeonju; Cristini, Vittorio et al. (2018) A Visually Apparent and Quantifiable CT Imaging Feature Identifies Biophysical Subtypes of Pancreatic Ductal Adenocarcinoma. Clin Cancer Res 24:5883-5894
Wilford, Justin; Osann, Kathryn; Hsieh, Susie et al. (2018) Validation of PROMIS emotional distress short form scales for cervical cancer. Gynecol Oncol 151:111-116
Bagaev, Alexander; Pichugin, Aleksey; Nelson, Edward L et al. (2018) Anticancer Mechanisms in Two Murine Bone Marrow-Derived Dendritic Cell Subsets Activated with TLR4 Agonists. J Immunol 200:2656-2669
Gong, Nian; Park, John; Luo, Z David (2018) Injury-induced maladaptation and dysregulation of calcium channel ?2 ? subunit proteins and its contribution to neuropathic pain development. Br J Pharmacol 175:2231-2243
Qiu, Xiaolong; Huang, Jen-Huang; Westerhof, Trisha M et al. (2018) Microfluidic channel optimization to improve hydrodynamic dissociation of cell aggregates and tissue. Sci Rep 8:2774
Kim, Seong M; Nguyen, Tricia T; Ravi, Archna et al. (2018) PTEN Deficiency and AMPK Activation Promote Nutrient Scavenging and Anabolism in Prostate Cancer Cells. Cancer Discov 8:866-883
Zhu, Yong; Wang, Xiuye; Forouzmand, Elmira et al. (2018) Molecular Mechanisms for CFIm-Mediated Regulation of mRNA Alternative Polyadenylation. Mol Cell 69:62-74.e4
Mishra, Birendra; Lawson, Gregory W; Ripperdan, Ryan et al. (2018) Charged-Iron-Particles Found in Galactic Cosmic Rays are Potent Inducers of Epithelial Ovarian Tumors. Radiat Res 190:142-150
Song, Wan; Zsindely, Nóra; Faragó, Anikó et al. (2018) Systematic genetic interaction studies identify histone demethylase Utx as potential target for ameliorating Huntington's disease. Hum Mol Genet 27:649-666
Lin, Xiaoxiao; Itoga, Christy A; Taha, Sharif et al. (2018) c-Fos mapping of brain regions activated by multi-modal and electric foot shock stress. Neurobiol Stress 8:92-102

Showing the most recent 10 out of 1106 publications