Core E - The principal objective of the Genomics and Sequencing (GS) Core of the Center for AIDS research (CFAR) at the University of California San Diego (UCSD) is to facilitate the research of HIV/AIDS investigators by providing cost-effective access to cutting-edge genomics and sequencing technologies. The GS Core will help investigators realize the enormous potential of these approaches to assist basic and applied research into the role of host and viral genes in HIV infection and pathogenesis, leading to new insights and treatments. Support for developmental projects and investigators new to HIV research is an area of special emphasis.
The specific aims of the GS Core are: (1) to develop and provide molecular tools and resources to HIV researchers for the determination of host and viral mechanisms of pathogenesis, (2) to guide HIV researchers in the value, use, and interpretation of genetic information and gene expression data, and (3) to facilitate education and training in genomics and sequencing technologies for CFAR investigators, students, staff, and other researchers. The GS Core will achieve these aims by providing: (1) assays for gene expression, viral detection and quantitation for research purposes, genetic variation, tools for functional genomics (e.g., siRNA expressing vectors), sequencing and/or deep sequencing of virus, host, transcriptome, or small RNAs, and provision of useful reagents to researchers, (2) analysis of gene expression and genetic variation, help with open source and proprietary tools for alignment and comparison of sequences, and collaboration with the Bioinformatics and Information Technologies (BIT) Core in molecular phylogeny studies, application-specific high throughput sequencing (HTS) pipelines, or more advanced data analysis, and (3) seminars, workshops, and individual training for graduate students and fellows, web resources, and mentoring of undergraduate independent study students. The GS Core will serve as an important resource for basic and translational HIV-related research, as best exemplified by 129 publications and 211 investigators supported by the combined services of the Genomics and Molecular Biology Cores since the last renewal. All evidence indicates the GS Core will be a valuable, productive, and popular basic science core for the UCSD CFAR.

Public Health Relevance

The Genomics and Sequencing (GS) Core of the Center for AIDS Research at UCSD provides HIV/AIDS researchers with access to the latest genomics technologies and sequencing applications for their research. The services performed by the GS Core provide information on the host and viral mechanisms of HIV associated disease. This in turn will lead to new treatments and interventions for HIV-infected individuals

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
5P30AI036214-20
Application #
8648958
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2014-04-01
Budget End
2015-03-31
Support Year
20
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Naticchia, Matthew R; Laubach, Logan K; Tota, Ember M et al. (2018) Embryonic Stem Cell Engineering with a Glycomimetic FGF2/BMP4 Co-Receptor Drives Mesodermal Differentiation in a Three-Dimensional Culture. ACS Chem Biol 13:2880-2887
Blumenthal, Jill; Jain, Sonia; Mulvihill, Evan et al. (2018) Perceived versus calculated HIV risk: Implications for Pre-exposure prophylaxis uptake in a randomized trial of men who have sex with men. J Acquir Immune Defic Syndr :
Kardava, Lela; Sohn, Haewon; Youn, Christine et al. (2018) IgG3 regulates tissue-like memory B cells in HIV-infected individuals. Nat Immunol 19:1001-1012
Wagner, Karla D; Syvertsen, Jennifer L; Verdugo, Silvia R et al. (2018) A mixed methods study of the social support networks of female sex workers and their primary noncommercial male partners in Tijuana, Mexico. J Mix Methods Res 12:437-457
Bastos, Francisco I; Bastos, Leonardo Soares; Coutinho, Carolina et al. (2018) HIV, HCV, HBV, and syphilis among transgender women from Brazil: Assessing different methods to adjust infection rates of a hard-to-reach, sparse population. Medicine (Baltimore) 97:S16-S24
Cepeda, Javier A; Eritsyan, Ksenia; Vickerman, Peter et al. (2018) Potential impact of implementing and scaling up harm reduction and antiretroviral therapy on HIV prevalence and mortality and overdose deaths among people who inject drugs in two Russian cities: a modelling study. Lancet HIV 5:e578-e587
Namazi, Golnaz; Fajnzylber, Jesse M; Aga, Evgenia et al. (2018) The Control of HIV After Antiretroviral Medication Pause (CHAMP) Study: Posttreatment Controllers Identified From 14 Clinical Studies. J Infect Dis 218:1954-1963
Lada, Steven M; Huang, Karissa; VanBelzen, D Jake et al. (2018) Quantitation of Integrated HIV Provirus by Pulsed-Field Gel Electrophoresis and Droplet Digital PCR. J Clin Microbiol 56:
Huang, Mia L; Michalak, Austen L; Fisher, Christopher J et al. (2018) Small Molecule Antagonist of Cell Surface Glycosaminoglycans Restricts Mouse Embryonic Stem Cells in a Pluripotent State. Stem Cells 36:45-54
Skaathun, Britt; Voisin, Dexter R; Cornwell, Benjamin et al. (2018) A Longitudinal Examination of Factors Associated with Network Bridging Among YMSM: Implications for HIV Prevention. AIDS Behav :

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