THIS COMPONENT IS ENTILTED THE GENOME TECHNOLOGY ACCESS CENTER SHARED RESOURCE ABSTRACT Project Summary Cancer genomics is widely studied and integral to the understanding, treatment and prevention of the disease. The genomic assays, tools, technology and expertise provided by the Genome Technology Access Center (GTAC) to Siteman Cancer Center (SCC) members enable researchers to advance in the fight against cancer. As GTAC is a SCC-supported facility, the close working relationship between GTAC staff and cancer researchers streamlines the design, execution and interpretation of all applied genomic assays. Furthermore, the dual nature of the GTAC, as both a research and CAP/CLIA-certified clinical genomics service provider, offers investigators a complete translational path for their research efforts. The GTAC provides next-generation sequencing, microarray analyses, and cutting-edge PCR services. Clinical sequencing, microarrays and PCR are performed in CAP/CLIA-certified laboratories. These technologies are leveraged for the analysis of gene transcription, DNA variant detection, DNA structural variation, genotyping, genome copy number and epigenetics. Assistance is available at all stages of a project, including experimental design, sample preparation, quality control, PCR/microarray/sequencing procedures, data clean-up and analysis. The GTAC occupies 5,875 sq. ft. of space located near the Center for Biomedical Informatics shared resource. GTAC is currently staffed by 22 scientists and maintains sufficient capacity to meet the needs of the Siteman Cancer Center research community.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA091842-14
Application #
8928320
Study Section
Subcommittee G - Education (NCI)
Project Start
2001-08-02
Project End
2020-07-31
Budget Start
2015-08-01
Budget End
2016-07-31
Support Year
14
Fiscal Year
2015
Total Cost
$238,439
Indirect Cost
$82,086
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Celik, Hamza; Koh, Won Kyun; Kramer, Ashley C et al. (2018) JARID2 Functions as a Tumor Suppressor in Myeloid Neoplasms by Repressing Self-Renewal in Hematopoietic Progenitor Cells. Cancer Cell 34:741-756.e8
Olfson, Emily; Bloom, Joseph; Bertelsen, Sarah et al. (2018) CYP2A6 metabolism in the development of smoking behaviors in young adults. Addict Biol 23:437-447
Betleja, Ewelina; Nanjundappa, Rashmi; Cheng, Tao et al. (2018) A novel Cep120-dependent mechanism inhibits centriole maturation in quiescent cells. Elife 7:
Chen, Li-Shiun; Horton, Amy; Bierut, Laura (2018) Pathways to precision medicine in smoking cessation treatments. Neurosci Lett 669:83-92
Jenkins, Wiley D; Gilbert, David; Chen, Li-Shiun et al. (2018) Finding paths with the greatest chance of success: enabling and focusing lung cancer screening and cessation in resource-constrained areas. Transl Lung Cancer Res 7:S261-S264
Kabir, Ashraf Ul; Lee, Tae-Jin; Pan, Hua et al. (2018) Requisite endothelial reactivation and effective siRNA nanoparticle targeting of Etv2/Er71 in tumor angiogenesis. JCI Insight 3:
Hirbe, Angela C; Jennings, Jack; Saad, Nael et al. (2018) A Phase II Study of Tumor Ablation in Patients with Metastatic Sarcoma Stable on Chemotherapy. Oncologist 23:760-e76
Burclaff, Joseph; Mills, Jason C (2018) Plasticity of differentiated cells in wound repair and tumorigenesis, part II: skin and intestine. Dis Model Mech 11:
Cherian, Mathew A; Olson, Sydney; Sundaramoorthi, Hemalatha et al. (2018) An activating mutation of interferon regulatory factor 4 (IRF4) in adult T-cell leukemia. J Biol Chem 293:6844-6858
Smith, Lee; Ae Lee, Jung; Mun, Junbae et al. (2018) Levels and patterns of self-reported and objectively-measured free-living physical activity among prostate cancer survivors: A prospective cohort study. Cancer :

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