The purpose of this Core is to provide bioinformafic analysis of transcriptomic, and DNA-protein interacfions. Next-generation sequencers have transformed genomic research, yet the analysis of this data remains a botfieneck. Our Core will provide the essenfial data analysis service to render this data accessible and interpretable to the members of this CORT. The PI and staff of this Core have extensive experience in the analysis of genomic data, as well as familiarity with the underiying biology of the associated projects. Despite the fact that microarray and sequencing cores exist at UCLA, none of these provide data analysis as a service. Therefore the typical biology group that does not have internal computational expertise is often left with data and no ability to interpret it. The Core we are proposing here will remove this impediment so that all the groups within this Program Project will be able to not only collect sequencing data from their samples, but also obtain processed and analyzed data that can be directly interpreted by researchers without computational expertise. This functionality should render genomics research far more accessible to all members of this Program Project. We will also work with more computafionally more experienced researchers in each lab of this Program to refine analysis tools.
The Aims of this Core are: 1. Analysis of RNA-seq data: we will provide quantificafion and variant detection analyses of RNA-seq data. 2. Analysis of ChlP-seq data: we will provide the locafion of peaks, average peak distribufions and motifs. 3. Data display on genome browser: in all cases this core will also load genome-wide data onto our installation of the UCSC genome browser so that users can see at single base resolufion the data generated from each sample. We will also upload data and analysis tools to the Wiki site for exchange. 4. Data Quality metrics: we will generate quality metrics for sequence data to provide an estimate of the quality of the sample.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Specialized Center (P50)
Project #
1P50AR063020-01
Application #
8343698
Study Section
Special Emphasis Panel (ZAR1-KM (M1))
Project Start
Project End
Budget Start
2012-08-16
Budget End
2013-07-31
Support Year
1
Fiscal Year
2012
Total Cost
$127,922
Indirect Cost
$39,455
Name
University of California Los Angeles
Department
Type
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Grasso, Catherine S; Giannakis, Marios; Wells, Daniel K et al. (2018) Genetic Mechanisms of Immune Evasion in Colorectal Cancer. Cancer Discov 8:730-749
Shieh, Albert; Ma, Christina; Chun, Rene F et al. (2018) Associations Between Change in Total and Free 25-Hydroxyvitamin D With 24,25-Dihydroxyvitamin D and Parathyroid Hormone. J Clin Endocrinol Metab 103:3368-3375
Keegan, Caroline; Krutzik, Stephan; Schenk, Mirjam et al. (2018) Mycobacterium tuberculosis Transfer RNA Induces IL-12p70 via Synergistic Activation of Pattern Recognition Receptors within a Cell Network. J Immunol 200:3244-3258
Madigan, Cressida A; Cambier, C J; Kelly-Scumpia, Kindra M et al. (2017) A Macrophage Response to Mycobacterium leprae Phenolic Glycolipid Initiates Nerve Damage in Leprosy. Cell 170:973-985.e10
Shieh, Albert; Ma, Christina; Chun, Rene F et al. (2017) Effects of Cholecalciferol vs Calcifediol on Total and Free 25-Hydroxyvitamin D and Parathyroid Hormone. J Clin Endocrinol Metab 102:1133-1140
Cheng, Christine S; Behar, Marcelo S; Suryawanshi, Gajendra W et al. (2017) Iterative Modeling Reveals Evidence of Sequential Transcriptional Control Mechanisms. Cell Syst 4:330-343.e5
Lopez, David; Montoya, Dennis; Ambrose, Michael et al. (2017) SaVanT: a web-based tool for the sample-level visualization of molecular signatures in gene expression profiles. BMC Genomics 18:824
Scumpia, Philip O; Botten, Giovanni A; Norman, Joshua S et al. (2017) Opposing roles of Toll-like receptor and cytosolic DNA-STING signaling pathways for Staphylococcus aureus cutaneous host defense. PLoS Pathog 13:e1006496
Purbey, Prabhat K; Scumpia, Philip O; Kim, Peter J et al. (2017) Defined Sensing Mechanisms and Signaling Pathways Contribute to the Global Inflammatory Gene Expression Output Elicited by Ionizing Radiation. Immunity 47:421-434.e3
Cunningham, Cameron R; Champhekar, Ameya; Tullius, Michael V et al. (2016) Type I and Type II Interferon Coordinately Regulate Suppressive Dendritic Cell Fate and Function during Viral Persistence. PLoS Pathog 12:e1005356

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