A fully Cancer Center-managed facility, the Genomics Technologies Shared Resource consists of theMicroarray and Molecular Cytogenetics facilities which provide access to specialized instrumentation andtechnical expertise in high-throughput genomic technologies and molecular cytogenetics for use inindividual and collaborative research programs. Services provided by the facility are: Microarray based genome-wide analysis of gene expression, genetic markers, and DNA copynumber aberrations Microarray based genome-wide analysis of chromatin modifications Validation of microarray and other data by high-throughput quantitative PCR Molecular cytogenetic analysis by fluorescence in situ hybridization (FISH) and spectral karyotyping(SKY) Evaluation and incorporation of emerging genomic technologies and promoting their integration intoresearch programs of HICCC investigators Investigator education and advice in adopting genome wide profiling and molecular cytogenetics intheir cancer research.The microarray component of the Genomics Technologies Shared Resource thus provides acomprehensive set of integrated genomic analysis tools and services that facilitate the high throughputanalysis of genetic and epigenetic alterations in human cancer in basic and translational researchprograms. These services, which are currently focused on procedures with several different microarrayplatforms from Affymetrix and Agilent, with ancillary methods including real-time PCR andPhosphorimaging, are closely linked to those provided by the Biomedical Informatics Shared Resource.The molecular cytogenetics facility provides SKY and FISH characterization of human and mouse tumorcells with efficient turnaround times utilizing state-of-the-art technologies. Together these facilities andservices provide an integrated platform for basic and translational genomics research in cancer biology atthe HICCC. Future plans include evaluating and potentially incorporating an ultra-high-throughputsequencing service into this Resource. During the last period of the CCSG, 53% of the investigators usingthe facility were Cancer Center members with peer-reviewed funding with those members representingfrom 50% to 98% of the usage of the available services. The proposed total operating budget of the facilityis $392,489, of which we are requesting $ 66,831 from the CCSG.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA013696-35
Application #
7669916
Study Section
Subcommittee G - Education (NCI)
Project Start
2008-08-01
Project End
2013-06-30
Budget Start
2008-08-01
Budget End
2009-06-30
Support Year
35
Fiscal Year
2008
Total Cost
$58,750
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Shang, Enyuan; Zhang, Yiru; Shu, Chang et al. (2018) Dual Inhibition of Bcl-2/Bcl-xL and XPO1 is synthetically lethal in glioblastoma model systems. Sci Rep 8:15383
Proto, Jonathan D; Doran, Amanda C; Subramanian, Manikandan et al. (2018) Hypercholesterolemia induces T cell expansion in humanized immune mice. J Clin Invest 128:2370-2375
Apatoff, Mary Ben L; Sengillo, Jesse D; White, Eugenia C et al. (2018) Autologous stem cell therapy for inherited and acquired retinal disease. Regen Med 13:89-96
Shen, Megan Johnson; Prigerson, Holly G; Ratshikana-Moloko, Mpho et al. (2018) Illness Understanding and End-of-Life Care Communication and Preferences for Patients With Advanced Cancer in South Africa. J Glob Oncol :1-9
Connors, Thomas J; Baird, J Scott; Yopes, Margot C et al. (2018) Developmental Regulation of Effector and Resident Memory T Cell Generation during Pediatric Viral Respiratory Tract Infection. J Immunol 201:432-439
Billing, David; Horiguchi, Michiko; Wu-Baer, Foon et al. (2018) The BRCT Domains of the BRCA1 and BARD1 Tumor Suppressors Differentially Regulate Homology-Directed Repair and Stalled Fork Protection. Mol Cell 72:127-139.e8
Wu, Hui-Chen; Do, Catherine; Andrulis, Irene L et al. (2018) Breast cancer family history and allele-specific DNA methylation in the legacy girls study. Epigenetics 13:240-250
Brescia, Paola; Schneider, Christof; Holmes, Antony B et al. (2018) MEF2B Instructs Germinal Center Development and Acts as an Oncogene in B Cell Lymphomagenesis. Cancer Cell 34:453-465.e9
Tzoneva, Gannie; Dieck, Chelsea L; Oshima, Koichi et al. (2018) Clonal evolution mechanisms in NT5C2 mutant-relapsed acute lymphoblastic leukaemia. Nature 553:511-514
Sitko, Austen A; Kuwajima, Takaaki; Mason, Carol A (2018) Eye-specific segregation and differential fasciculation of developing retinal ganglion cell axons in the mouse visual pathway. J Comp Neurol 526:1077-1096

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