A computational framework for global analysis of translation regulation
A computational framework for global analysis of translation regulation
批准号:
8883005
负责人:
Luiz Otavio Penalva
金额:
$44.0万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-13 至 2018-07-31
关键词:
AddressAdoptedBehaviorBiologicalBiological AssayCell CycleCellsCommunitiesComplexComputer AnalysisComputer softwareComputing MethodologiesDataData SetDevelopmentDiseaseEnsureEvaluationFundingGene ExpressionGene StructureGenetic TranscriptionGenomicsKnowledgeLinkMeasuresMessenger RNAMethodologyMethodsModelingOpen Reading FramesOutcomes ResearchPhenotypePrintingPropertyProtein BindingProteinsRNA-Binding ProteinsRNA-Protein InteractionRadiationRegulationResearchResearch PersonnelRibosomesRoleRunningScientistSeriesSiteSpeedStagingStatistical MethodsStatistical ModelsStructureTechnologyTestingThe SunTimeTranscriptional RegulationTranslatingTranslational RegulationTranslationsWorkbasecell typecomputer frameworkcomputerized toolscrosslinking and immunoprecipitation sequencingfootgenome-wideimprovedmeetingsmethod developmentmolecular phenotypenew technologypublic health relevanceresearch studysuccesstooltranscriptome sequencing
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Ribosome profiling delivers quantitative information on the number and behavior of translating ribosomes, and gives profiles of gene expression much more closely linked to actual protein levels. The ribosomal profiling technology, however, is not yet widely adopted, and a major reason is that essential computational methods for analyzing ribosomal profiling data are lacking. Through this project we will develop a computational framework to address a set of specific problems in analyzing ribosomal profiling data, including data-driven ORF identification, correcting measures of translation for the influence of ribosome stalling, and a probabilistic model to estimate ribosome elongation speed from time-series data. Specific experiments will be conducted to support and challenge the development of computational methods, and major refinements to existing experimental technology for conducting ribosomal foot-printing will also be developed. Ultimately, through completing the aims of this proposal, we will take major steps in bringing ribosomal profiling technology into broader use in defining molecular phenotypes of cells.
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海外基金