The Bioinformatics Core was established in 2007 to provide analytical support for numerous research projects at the Joslin Diabetes Center. Core activities and resources including biostatistics consulting, the clinical data warehouse, the high-performance computer cluster and the analysis of genomic data have benefited most labs at Joslin. The recent emergence of new technologies for high-throughput DNA sequencing, metabolomics, and proteomics among others catalyzed transformative changes throughout the biomedical sciences. The need to introduce these whole genome technologies into diabetes research brings numerous informatics and systems biology challenges. Computational science, network modeling and informatics play important roles in meeting these challenges. We propose an expanded Computational Core that will significantly enhance our analytic capabilities in order to cover not only basic support functions but also to promote innovative network modeling and systems biology approaches to diabetes research at Joslin and throughout the Boston area. The proposed Core is named the Boston University Joslin Regional Computational Core (BUJRC Core) and will consist of two branches: the Bioinformatics / Computational Biology Service branch and the Collaborative Systems Biology/Medicine branch. The Bioinformatics / Computational Biology Service branch will act as a resource to the diabetes research community by providing state-of the-art analysis of high-throughput biomedical data, as well as consultation on the design of these types of experiments. This branch will support diabetes research in the design, analysis, and biological interpretation of experiments that involve generation of """"""""omic"""""""" data and its integration with physiological and clinical data. The Collaborative Systems Biology/Medicine branch will help to create an environment that incorporates computational systems biology/medicine methodologies into clinically relevant translational and basic diabetes research. This branch includes local faculty with a proven track record of having worked together to produce innovative systems biology and translational research. This proposed expanded Core will significantly enhance the prior capabilities to provide support functions to Joslin researchers as well as developing relevant network modeling and systems biology methodologies at Boston University. The expanded core will serve as a bridge for establishing collaborations with other diabetes researchers throughout the region.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK036836-28
Application #
8725126
Study Section
Special Emphasis Panel (ZDK1-GRB-S)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
28
Fiscal Year
2014
Total Cost
$318,217
Indirect Cost
$62,950
Name
Joslin Diabetes Center
Department
Type
DUNS #
071723084
City
Boston
State
MA
Country
United States
Zip Code
02215
Mulla, Christopher M; Middelbeek, Roeland J W; Patti, Mary-Elizabeth (2018) Mechanisms of weight loss and improved metabolism following bariatric surgery. Ann N Y Acad Sci 1411:53-64
Skupien, Jan; Smiles, Adam M; Valo, Erkka et al. (2018) Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced Nephropathy. Diabetes Care :
Laffel, L (2018) Lost in transition: finding a path forward for young adults with Type 1 diabetes. Diabet Med 35:1061-1062
Rao, Tata Nageswara; Gupta, Manoj K; Softic, Samir et al. (2018) Attenuation of PKC? enhances metabolic activity and promotes expansion of blood progenitors. EMBO J 37:
Bauman, Viviana; Sturkey, Adaya C; Sherafat-Kazemzadeh, Rosa et al. (2018) Factitious hypoglycemia in children and adolescents with diabetes. Pediatr Diabetes 19:823-831
Stanford, Kristin I; Rasmussen, Morten; Baer, Lisa A et al. (2018) Paternal Exercise Improves Glucose Metabolism in Adult Offspring. Diabetes 67:2530-2540
Park, Kyoungmin; Li, Qian; Evcimen, Net Da? et al. (2018) Exogenous Insulin Infusion Can Decrease Atherosclerosis in Diabetic Rodents by Improving Lipids, Inflammation, and Endothelial Function. Arterioscler Thromb Vasc Biol 38:92-101
Lynes, Matthew D; Shamsi, Farnaz; Sustarsic, Elahu Gosney et al. (2018) Cold-Activated Lipid Dynamics in Adipose Tissue Highlights a Role for Cardiolipin in Thermogenic Metabolism. Cell Rep 24:781-790
Schuster, Cornelia; Jonas, Franziska; Zhao, Fangzhu et al. (2018) Peripherally induced regulatory T cells contribute to the control of autoimmune diabetes in the NOD mouse model. Eur J Immunol 48:1211-1216
Laguna Sanz, Alejandro J; Mulla, Christopher M; Fowler, Kristen M et al. (2018) Design and Clinical Evaluation of a Novel Low-Glucose Prediction Algorithm with Mini-Dose Stable Glucagon Delivery in Post-Bariatric Hypoglycemia. Diabetes Technol Ther 20:127-139

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