BIOINFORMATICS SHARED RESOURCE The Bioinformatics SR (BIOIN) is a vital component of the Center?s entire research operation. It houses all databases, date storage, and analytic infrastructure central to Lineberger?s research. Two major functions of the SR are 1) the maintenance of all databases, substantial computational and data storage infrastructure in a secure yet utilitarian computing environment and; 2) a full complement of research services to faculty for ?big data? analysis and the development of new analytic techniques. An example of these services includes the management of the Laboratory Information Management System (LIMS) used for tissue tracking which promotes the seamless transfer of samples from group to group. The LIMS integrates with other applications such as the Lineberger Data & Biospecimens Repository and Tableau for report generation. LIMS currently supports 10 SR, encompassing 7,628 active protocols, and 2.5M containers. The SR is central to the handling and analysis of tissue-based clinical genomics studies such as UNCsequel and those 9 institutional trials. The facility is a primary partner for faculty in sequencing processes for DNA and RNA and drive new tools for discovery and results in publications such as Perou & Parker, Bioinformatics 2019,and Kim et al. Nat Methods, 2018) Another example is the involvement of BIOIN in every TCGA paper since 2016 (48 in total). BIOIN request a CCSG budget of $264,702 which represents 8% of its operating costs and is requested to support the salary of key personnel for effort in support of cancer research and bioinformatic analysis. This facility was used by nearly 100 members for bioinformatics analysis in fiscal year 2019. The facility is a Lineberger exclusive resource and as such the users were 100% members in 2019. The import of the core and its scientific infrastructure is illustrated by the ~$3.5M annual LCCC investment in its operation.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA016086-45
Application #
10089831
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
1997-06-01
Project End
2025-11-30
Budget Start
2020-12-01
Budget End
2021-11-30
Support Year
45
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Curtis 2nd, Alan D; Jensen, Kara; Van Rompay, Koen K A et al. (2018) A simultaneous oral and intramuscular prime/sublingual boost with a DNA/Modified Vaccinia Ankara viral vector-based vaccine induces simian immunodeficiency virus-specific systemic and mucosal immune responses in juvenile rhesus macaques. J Med Primatol 47:288-297
Williams, Lindsay A; Nichols, Hazel B; Hoadley, Katherine A et al. (2018) Reproductive risk factor associations with lobular and ductal carcinoma in the Carolina Breast Cancer Study. Cancer Causes Control 29:25-32
Amunugama, Ravindra; Willcox, Smaranda; Wu, R Alex et al. (2018) Replication Fork Reversal during DNA Interstrand Crosslink Repair Requires CMG Unloading. Cell Rep 23:3419-3428
Little, Michael S; Pellock, Samuel J; Walton, William G et al. (2018) Structural basis for the regulation of ?-glucuronidase expression by human gut Enterobacteriaceae. Proc Natl Acad Sci U S A 115:E152-E161
Knott, Simon R V; Wagenblast, Elvin; Khan, Showkhin et al. (2018) Erratum: Asparagine bioavailability governs metastasis in a model of breast cancer. Nature 556:135
Anderson, Chelsea; Smitherman, Andrew B; Nichols, Hazel B (2018) Conditional relative survival among long-term survivors of adolescent and young adult cancers. Cancer 124:3037-3043
Liu, Meng-Xi; Jin, Lei; Sun, Si-Jia et al. (2018) Metabolic reprogramming by PCK1 promotes TCA cataplerosis, oxidative stress and apoptosis in liver cancer cells and suppresses hepatocellular carcinoma. Oncogene 37:1637-1653
Chai, Zheng; Zhang, Xintao; Rigsbee, Kelly Michelle et al. (2018) Cryoprecipitate augments the global transduction of the adeno-associated virus serotype 9 after a systemic administration. J Control Release 286:415-424
Butler, Kyle V; Chiarella, Anna M; Jin, Jian et al. (2018) Targeted Gene Repression Using Novel Bifunctional Molecules to Harness Endogenous Histone Deacetylation Activity. ACS Synth Biol 7:38-45
Zhang, Yang; Hwang, Bin-Jin; Liu, Zhen et al. (2018) BP180 dysfunction triggers spontaneous skin inflammation in mice. Proc Natl Acad Sci U S A 115:6434-6439

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