This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Infrastructure: CORE C: Bioinformatics in Viral Molecular Biology Marjan Trutschl High-throughput technologies have established themselves as indispensable tools for the study of biological systems, from gene expression level changes, protein concentrations, to their modifications and interactions in complex diseases and systems ?cells and complete organisms. Core C, focused on bioinformatics, is new for the COBRE project. The faculty of the Core has collaborated on several projects with COBRE-related faculty through the Microarray Facility at LSUHSC-S. The demand for the bioinformatics services grew with the number of microarrays processed. The Core assists with computational aspects of the COBRE projects, including all aspects of statistical and high-throughput analyses, such as experimental design, data standardization and normalization, pathway and other confirmatory analyses, data storage, sharing and management and integration of the project-related data into public databases. The main goal of this core is to incorporate aspects of high-throughput and high-performance computing with knowledge discovery approaches through the application of neural networks, probability and statistics to support and enhance each of the participating projects and Core B. Core C facilitates the multi-step, data-intensive nature of the knowledge discovery process, utilizing the latest tools and techniques as applied to the COBRE projects.
Three aims lead the activities of the Core's activities:
Aim 1 : SERVICE: create a structure of support Aim 2: RESEARCH AND DEVELOPMENT: new techniques and algorithms that supplement currently available off-the shelf and open-source packages Aim 3: EDUCATION: introduce and train young and established investigators in the technologies available in the field of bioinformatics.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR018724-08
Application #
8167466
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2010-05-01
Project End
2011-04-30
Budget Start
2010-05-01
Budget End
2011-04-30
Support Year
8
Fiscal Year
2010
Total Cost
$194,970
Indirect Cost
Name
Louisiana State University Hsc Shreveport
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
095439774
City
Shreveport
State
LA
Country
United States
Zip Code
71103
Kim, Jung Heon; Collins-McMillen, Donna; Buehler, Jason C et al. (2017) Human Cytomegalovirus Requires Epidermal Growth Factor Receptor Signaling To Enter and Initiate the Early Steps in the Establishment of Latency in CD34+ Human Progenitor Cells. J Virol 91:
Martinez, Nicholas E; Sato, Fumitaka; Kawai, Eiichiro et al. (2015) Th17-biased ROR?t transgenic mice become susceptible to a viral model for multiple sclerosis. Brain Behav Immun 43:86-97
Kawai, Eiichiro; Sato, Fumitaka; Omura, Seiichi et al. (2015) Organ-specific protective role of NKT cells in virus-induced inflammatory demyelination and myocarditis depends on mouse strain. J Neuroimmunol 278:174-84
Stevenson, Emily V; Collins-McMillen, Donna; Kim, Jung Heon et al. (2014) HCMV reprogramming of infected monocyte survival and differentiation: a Goldilocks phenomenon. Viruses 6:782-807
Coleman, Carrie B; McGraw, Jennifer E; Feldman, Emily R et al. (2014) A gammaherpesvirus Bcl-2 ortholog blocks B cell receptor-mediated apoptosis and promotes the survival of developing B cells in vivo. PLoS Pathog 10:e1003916
Fernando, Viromi; Omura, Seiichi; Sato, Fumitaka et al. (2014) Regulation of an autoimmune model for multiple sclerosis in Th2-biased GATA3 transgenic mice. Int J Mol Sci 15:1700-18
Martinez, Nicholas E; Karlsson, Fridrik; Sato, Fumitaka et al. (2014) Protective and detrimental roles for regulatory T cells in a viral model for multiple sclerosis. Brain Pathol 24:436-51
Sato, Fumitaka; Omura, Seiichi; Kawai, Eiichiro et al. (2014) Distinct kinetics of viral replication, T cell infiltration, and fibrosis in three phases of myocarditis following Theiler's virus infection. Cell Immunol 292:85-93
DiGiuseppe, Stephen; Bienkowska-Haba, Malgorzata; Hilbig, Lydia et al. (2014) The nuclear retention signal of HPV16 L2 protein is essential for incoming viral genome to transverse the trans-Golgi network. Virology 458-459:93-105
Sato, Fumitaka; Martinez, Nicholas E; Shahid, Maira et al. (2013) Resveratrol exacerbates both autoimmune and viral models of multiple sclerosis. Am J Pathol 183:1390-1396

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