Recent technological advances in high-throughput experimental analysis enable modern biologists to? collect data at the genome scale, and use them to decipher biological principles and uncover the elements? of complex behaviors in living organisms. The advances and changes in the research paradigm require? development of a set of tools that biologists need for scientific discovery. Among these, computational and? data analysis tools are essential, and are largely provided by the fields of data mining, bioinformatics and? statistics. We propose to introduce a new approach to functional genomics studies, and hypothesize that? the global expression profile of any organism could provide a universal phenotype for direct prediction of? biological function. We will develop a set of computational tools to treat such phenotypes, perform the? corresponding data analyses and infer predictive functional models from experimental data. Our efforts will? be based on an arsenal of state-of-the-art data mining approaches. We will adapt existing tools and? develop new ones to help us infer reliable predictions, to find what biological changes took place following? environmental or genetic change, and to explain the relevant biological background. Our methods will infer? interactions between global expression profiles, mutant fitness, gene function and annotation, and classical? biological phenotypes, such as chemotaxis, morphogenesis and development. Using correlation studies,? the methods will decompose expression profiles to biologically meaningful components that will enable us? to reason on the functional changes and their relations at the genome scale. Most importantly, we will test? and adjust these tools in collaboration with the biological projects, ensuring their practical utility. We will? package our methods into open-source toolboxes, using component-based design and a visual? programming paradigm to make the tools accessible to users that are not programmers or computer? experts. We will make that package freely available to the research community. This project will also define? and maintain the information infrastructure for the entire program, and will provide databases that will store? experimental information and related data on hundreds of mutants. Finally, we will develop server-based? software to provide public access to the vast amounts of data produced by this program and to selected? data analysis tools through the world wide web.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
5P01HD039691-08
Application #
7646348
Study Section
Pediatrics Subcommittee (CHHD)
Project Start
Project End
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
8
Fiscal Year
2008
Total Cost
$218,603
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
051113330
City
Houston
State
TX
Country
United States
Zip Code
77030
Dinh, Christopher; Farinholt, Timothy; Hirose, Shigenori et al. (2018) Lectins modulate the microbiota of social amoebae. Science 361:402-406
Hirose, Shigenori; Chen, Gong; Kuspa, Adam et al. (2017) The polymorphic proteins TgrB1 and TgrC1 function as a ligand-receptor pair in Dictyostelium allorecognition. J Cell Sci 130:4002-4012
Swatson, William S; Katoh-Kurasawa, Mariko; Shaulsky, Gad et al. (2017) Curcumin affects gene expression and reactive oxygen species via a PKA dependent mechanism in Dictyostelium discoideum. PLoS One 12:e0187562
Stajdohar, Miha; Rosengarten, Rafael D; Kokosar, Janez et al. (2017) dictyExpress: a web-based platform for sequence data management and analytics in Dictyostelium and beyond. BMC Bioinformatics 18:291
Rosengarten, Rafael D; Santhanam, Balaji; Kokosar, Janez et al. (2017) The Long Noncoding RNA Transcriptome of Dictyostelium discoideum Development. G3 (Bethesda) 7:387-398
Zhang, Xuezhi; Zhuchenko, Olga; Kuspa, Adam et al. (2016) Social amoebae trap and kill bacteria by casting DNA nets. Nat Commun 7:10938
Zitnik, Marinka; Zupan, Blaz (2016) COLLECTIVE PAIRWISE CLASSIFICATION FOR MULTI-WAY ANALYSIS OF DISEASE AND DRUG DATA. Pac Symp Biocomput 21:81-92
Katoh-Kurasawa, Mariko; Santhanam, Balaji; Shaulsky, Gad (2016) The GATA transcription factor gene gtaG is required for terminal differentiation in Dictyostelium. J Cell Sci :
Zitnik, Marinka; Zupan, Blaz (2016) Jumping across biomedical contexts using compressive data fusion. Bioinformatics 32:i90-i100
Chen, Xinlu; Köllner, Tobias G; Jia, Qidong et al. (2016) Terpene synthase genes in eukaryotes beyond plants and fungi: Occurrence in social amoebae. Proc Natl Acad Sci U S A 113:12132-12137

Showing the most recent 10 out of 64 publications