The goal of the bioinformatics/biostatistics core is to address the bioinformatics, statistical and datamanagement needs of the participating SPORE projects. To this end, the bioinformatics/biostatistics corewill work in close collaboration with existing Yale informatics resources, projects and research groups. Thecore is also tightly integrated with the SPORE specimen resource core for the development of a tissuetracking and annotation system.
The specific aims of the bioinformatics/biostatistics core are 1) thebioinformatics and statistical analysis of SPORE project data and 2) the design, building and maintenanceof a SPORE data management and analysis system (SPORE-DMAS). For 1), an important focus is theclose interaction with the project investigators during the entire duration of the SPORE program. The corewill provide continuous analysis services such as protocol design, data annotation and visualization. Theanalyses will chiefly focus on projects 1,2 and 4, which concern the elucidation of risk factors for earlyonset BCC patients, the detection of predictive epigenomic markers in metastatic melanoma cells, as wellas establishing the serological profiles of melanoma patients. For 2), the core will design, build andmaintain a SPORE data management and analysis system (SPORE-DMAS) for tracking of biologicalspecimens, and processing of clinical and experimental data. The SPORE-DMAS will be tightly integratedinto SPORE specimen resource core, and will handle the data management needs of the SPORE projectmembers. The SPORE-DMAS will make extensive use of existing informatics systems at Yale University,and of resources from caBIG's Tissue Banks and Pathology Tools Workspace. The core will also beconcerned with making data available according to the SPORE data and resource sharing plan.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
1P50CA121974-01
Application #
7147305
Study Section
Special Emphasis Panel (ZCA1-GRB-I (M1))
Project Start
2006-06-01
Project End
2011-05-31
Budget Start
2006-06-01
Budget End
2007-06-30
Support Year
1
Fiscal Year
2006
Total Cost
$176,342
Indirect Cost
Name
Yale University
Department
Type
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Krauthammer, Michael (2018) Unraveling the etiology of primary malignant melanoma of the esophagus. J Thorac Dis 10:S1074-S1075
Das, Rituparna; Bar, Noffar; Ferreira, Michelle et al. (2018) Early B cell changes predict autoimmunity following combination immune checkpoint blockade. J Clin Invest 128:715-720
Ferrucci, Leah M; Cartmel, Brenda; Clare, Rachel A et al. (2018) Cross-sectional assessment of ultraviolet radiation-related behaviors among young people after a diagnosis of melanoma or basal cell carcinoma. J Am Acad Dermatol 79:149-152
Arbesman, Joshua; Ravichandran, Sairekha; Funchain, Pauline et al. (2018) Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations. Pigment Cell Melanoma Res 31:529-533
Perry, Curtis J; Muñoz-Rojas, Andrés R; Meeth, Katrina M et al. (2018) Myeloid-targeted immunotherapies act in synergy to induce inflammation and antitumor immunity. J Exp Med 215:877-893
Liu, Xiaoni; Zhang, Shang-Min; McGeary, Meaghan K et al. (2018) KDM5B Promotes Drug Resistance by Regulating Melanoma Propagating Cell Subpopulations. Mol Cancer Ther :
Sulkowski, Parker L; Scanlon, Susan E; Oeck, Sebastian et al. (2018) PTEN Regulates Nonhomologous End Joining By Epigenetic Induction of NHEJ1/XLF. Mol Cancer Res 16:1241-1254
Chen, Ling; Azuma, Takeshi; Yu, Weiwei et al. (2018) B7-H1 maintains the polyclonal T cell response by protecting dendritic cells from cytotoxic T lymphocyte destruction. Proc Natl Acad Sci U S A 115:3126-3131
Miller, Chad J; Muftuoglu, Yagmur; Turk, Benjamin E (2017) A high throughput assay to identify substrate-selective inhibitors of the ERK protein kinases. Biochem Pharmacol 142:39-45
Kluger, Harriet M; Zito, Christopher R; Turcu, Gabriela et al. (2017) PD-L1 Studies Across Tumor Types, Its Differential Expression and Predictive Value in Patients Treated with Immune Checkpoint Inhibitors. Clin Cancer Res 23:4270-4279

Showing the most recent 10 out of 172 publications