The overall objectives of the DNA Microarray Shared Resource are to provide comprehensive services to investigators performing genome-scale expression profiling experiments and to provide informatics support in the analysis of high-density gone expression data sets. Services offered in the Shared Resource are divided into three segments: 1) Reagents and Supplies; 2) Experimental Support; and 3) Data Analysis and Support. Reagents and Supplies include the generation of high-density mouse, human, and yeast cDNA microarrays containing from 6,600 to 28,000 elements, stocking of arrays and reagents for several array platforms, maintenance and distribution for NIA clone sets, and production and stocking of specialty reagents for gene expression profiling experiments. Experimental Support includes experimental design consultation and evaluation, RNA processing and quality control, fluorescently labeled target production, and high-density array hybridization using varied microarrays. Data and Analysis Support includes scanning and image analysis of the hybridized arrays, processing of the raw data sets, comprehensive bioinformatics support for the analysis and annotation of the resulting expression data sets, data formatting and transfer to other Shared Resources when appropriate, development of web-based supplements in support of grants and publications, and the back-up and archiving of all data sets produced in the Shared Resource. Dr. Shawn Levy is Scientific Director of the DNA Microarray Shared Resource and offers experimental design consultation to investigators, reviews and approves requests for custom or boutique arrays, and is involved in the development and optimization of new services. Dr. Levy assists investigators in the use of higher-order analysis tools such as clustering, multi-dimensional scaling and evaluation of statistical significance, and also offers training on all Shared Resource services.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA068485-09
Application #
6990139
Study Section
Subcommittee G - Education (NCI)
Project Start
2004-09-28
Project End
2009-08-31
Budget Start
2004-09-28
Budget End
2005-08-31
Support Year
9
Fiscal Year
2004
Total Cost
$115,076
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Vierra, Nicholas C; Dickerson, Matthew T; Jordan, Kelli L et al. (2018) TALK-1 reduces delta-cell endoplasmic reticulum and cytoplasmic calcium levels limiting somatostatin secretion. Mol Metab 9:84-97
Schlegel, Cameron; Weis, Victoria G; Knowles, Byron C et al. (2018) Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease. Dig Dis Sci 63:356-365
Lewis Jr, James S; Shelton, Jeremy; Kuhs, Krystle Lang et al. (2018) p16 Immunohistochemistry in Oropharyngeal Squamous Cell Carcinoma Using the E6H4 Antibody Clone: A Technical Method Study for Optimal Dilution. Head Neck Pathol 12:440-447
Werfel, Thomas A; Wang, Shan; Jackson, Meredith A et al. (2018) Selective mTORC2 Inhibitor Therapeutically Blocks Breast Cancer Cell Growth and Survival. Cancer Res 78:1845-1858
Heaster, Tiffany M; Walsh, Alex J; Zhao, Yue et al. (2018) Autofluorescence imaging identifies tumor cell-cycle status on a single-cell level. J Biophotonics 11:
PiƱeros, Marion; Frech, Silvina; Frazier, Lindsay et al. (2018) Advancing Reliable Data for Cancer Control in the Central America Four Region. J Glob Oncol :1-11
Schulte, Michael L; Fu, Allie; Zhao, Ping et al. (2018) Pharmacological blockade of ASCT2-dependent glutamine transport leads to antitumor efficacy in preclinical models. Nat Med 24:194-202
Petersen, Christine P; Meyer, Anne R; De Salvo, Carlo et al. (2018) A signalling cascade of IL-33 to IL-13 regulates metaplasia in the mouse stomach. Gut 67:805-817
Maacha, Selma; Hong, Jun; von Lersner, Ariana et al. (2018) AXL Mediates Esophageal Adenocarcinoma Cell Invasion through Regulation of Extracellular Acidification and Lysosome Trafficking. Neoplasia 20:1008-1022
Galligan, James J; Wepy, James A; Streeter, Matthew D et al. (2018) Methylglyoxal-derived posttranslational arginine modifications are abundant histone marks. Proc Natl Acad Sci U S A 115:9228-9233

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