The Genomics Core produces DNA microarrays through high throughput automation, and involves robotic production and spotting of either cDNA or oligonucleotides onto glass slides. The core functions primarily to serve Buck investigators and outside users, in both the design and analysis of microarray experiments. The resources available include: cDNA chips for mice and fly, oligo chips for humans, mice, and worms, and the appropriate instrumentation to prepare, spot, hybridize, quantitate and analyze microarray chips from these diverse species. Archiving of data generated by the core is accomplished by uploading the quantitated data files into Genetraffic (a commercially available package), which facilitates remote retrieval of the relevant data via a password protected system, as well as rudimentary analysis of differential gene expression. Over the last several years, the core has also developed expertise in using academically developed statistical analysis modules, specifically designed for the analysis of microarray data. All these packages are free, and are developed and maintained in the computing environment """"""""R"""""""", and listed at the bioconductor website (www.bioconductor.org).The Core is currently promoting aging research within the institute by providing service to a number of laboratories, and this has resulted in a several publications. The Buck Institute Genomics Core also currently serves outside users by providing microarray expertise and service for studies related to aging and age-related disease.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
5P30AG025708-05
Application #
7892310
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
5
Fiscal Year
2009
Total Cost
$159,960
Indirect Cost
Name
Buck Institute for Age Research
Department
Type
DUNS #
786502351
City
Novato
State
CA
Country
United States
Zip Code
94945
Guyenet, Stephan J; Mookerjee, Shona S; Lin, Amy et al. (2015) Proteolytic cleavage of ataxin-7 promotes SCA7 retinal degeneration and neurological dysfunction. Hum Mol Genet 24:3908-17
Flynn, James M; Melov, Simon (2013) SOD2 in mitochondrial dysfunction and neurodegeneration. Free Radic Biol Med 62:4-12
Chen, Di; Li, Patrick Wai-Lun; Goldstein, Benjamin A et al. (2013) Germline signaling mediates the synergistically prolonged longevity produced by double mutations in daf-2 and rsks-1 in C. elegans. Cell Rep 5:1600-10
Miller, John P; Yates, Bridget E; Al-Ramahi, Ismael et al. (2012) A genome-scale RNA-interference screen identifies RRAS signaling as a pathologic feature of Huntington's disease. PLoS Genet 8:e1003042
Flynn, James M; Czerwieniec, Gregg A; Choi, Sung W et al. (2012) Proteogenomics of synaptosomal mitochondrial oxidative stress. Free Radic Biol Med 53:1048-60
Goehring, Isabel; Gerencser, Akos A; Schmidt, Sara et al. (2012) Plasma membrane potential oscillations in insulin secreting Ins-1 832/13 cells do not require glycolysis and are not initiated by fluctuations in mitochondrial bioenergetics. J Biol Chem 287:15706-17
Katewa, Subhash D; Demontis, Fabio; Kolipinski, Marysia et al. (2012) Intramyocellular fatty-acid metabolism plays a critical role in mediating responses to dietary restriction in Drosophila melanogaster. Cell Metab 16:97-103
Mookerjee, Shona A; Brand, Martin D (2011) Characteristics of the turnover of uncoupling protein 3 by the ubiquitin proteasome system in isolated mitochondria. Biochim Biophys Acta 1807:1474-81
Powolny, Anna A; Singh, Shivendra V; Melov, Simon et al. (2011) The garlic constituent diallyl trisulfide increases the lifespan of C. elegans via skn-1 activation. Exp Gerontol 46:441-52
Flynn, James M; Choi, Sung W; Day, Nicholas U et al. (2011) Impaired spare respiratory capacity in cortical synaptosomes from Sod2 null mice. Free Radic Biol Med 50:866-73

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