The Molecular Profiling Core (Core C) integrates with and enhances the capabilities of our existing Biotechnology Support Facility, Microarray Facility and new Genome Sequencing Facility, the first two with histories of success in augmenting and extending the research programs of investigators at KUMC. This core will assist COBRE investigators by providing cost-effective services for the synthesis of oligonucleotides, DNA sequence analysis, microarray chip processing and genome sequencing technologies. Eighty-three percent of our Center Members/Mentors (24/29) and 4 of the 5 previous cycle COBRE Beginning Investigators utilized these facilities during the last funding period. During the next funding period, there will be 5 Beginning Investigators and 29 Center Members/Mentors. The expectation is that usage will increase during the upcoming grant cycle. Historically, usage by this group of researchers accounts for 22% of all KUMC oligonucleotide synthesis, 97% of DNA sequencing and 33% of microarray chip analysis on an annual basis. A significant portion of this same faculty anticipates utilizing recently acquired NexGen sequencing capabilities. This facility will provide all COBRE scientists with services to synthesize oligonucleotides, obtain DNA sequence determination and analysis, supply microan-ay chips and chip processing technologies, and offer the latest genomic deep sequencing methodologies to center investigators. The COBRE funds will subsidize activities for the junior investigators and for members of the Center who use the core, and the institution will continue to provide significant state support for this facility. The Biotechnology Support Facility is staffed by a lab manager and three personnel. One of these personnel also serves as the project manager of the Microarray Facility and Project Supervisor of the Genome Sequencing Facility. All are experts with the methods required and will interface with the COBRE Molecular Profiling Core Director. The addition of services offered by the newly-established Genome Sequencing Facility's lllumina HiSeq 2000 Sequencing System will accelerate COBRE investigator research by performing large-scale sequencing studies on complex genomes, transcriptomes and epigenomes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM104936-07
Application #
8534217
Study Section
Special Emphasis Panel (ZRR1-RI-B)
Project Start
Project End
Budget Start
2013-07-01
Budget End
2014-06-30
Support Year
7
Fiscal Year
2013
Total Cost
$225,262
Indirect Cost
$76,082
Name
University of Kansas
Department
Type
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Yang, Fu-Chen; Draper, Julia; Smith, Peter G et al. (2018) Short Term Development and Fate of MGE-Like Neural Progenitor Cells in Jaundiced and Non-Jaundiced Rat Brain. Cell Transplant 27:654-665
Kumar, Dhruv; Yalamanchali, Sreeya; New, Jacob et al. (2018) Development and Characterization of an In Vitro Model for Radiation-Induced Fibrosis. Radiat Res 189:326-336
Jack, Brittany; Avasthi, Prachee (2018) Chemical Screening for Flagella-Associated Phenotypes in Chlamydomonas reinhardtii. Methods Mol Biol 1795:203-221
Freitas, Natalia; Lukash, Tetyana; Gunewardena, Sumedha et al. (2018) Relative Abundance of Integrant-Derived Viral RNAs in Infected Tissues Harvested from Chronic Hepatitis B Virus Carriers. J Virol 92:
Kumar, T Rajendra (2018) Fshb Knockout Mouse Model, Two Decades Later and Into the Future. Endocrinology 159:1941-1949
Cao, Thuy; Rajasingh, Sheeja; Samanta, Saheli et al. (2018) Biology and clinical relevance of noncoding sno/scaRNAs. Trends Cardiovasc Med 28:81-90
Kumar, Ram P; Ray, Soma; Home, Pratik et al. (2018) Regulation of energy metabolism during early mammalian development: TEAD4 controls mitochondrial transcription. Development 145:
Samanta, Saheli; Rajasingh, Sheeja; Drosos, Nicholas et al. (2018) Exosomes: new molecular targets of diseases. Acta Pharmacol Sin 39:501-513
Chao, Xiaojuan; Wang, Shaogui; Zhao, Katrina et al. (2018) Impaired TFEB-Mediated Lysosome Biogenesis and Autophagy Promote Chronic Ethanol-Induced Liver Injury and Steatosis in Mice. Gastroenterology 155:865-879.e12
Srivastava, Tarak; Dai, Hongying; Heruth, Daniel P et al. (2018) Mechanotransduction signaling in podocytes from fluid flow shear stress. Am J Physiol Renal Physiol 314:F22-F34

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