Modeling phenotypic transitions in gene expression state space
Modeling phenotypic transitions in gene expression state space
批准号:
8326605
负责人:
Megha Padi
金额:
$11.94万
依托单位:
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:
2011-09-01 至 2016-05-31
关键词:
AdhesionsAffectBiologicalBiological AssayBiologyBiomedical ResearchBypassCatalogingCatalogsCell LineCellsCessation of lifeComputational BiologyComputer SimulationDataData SetDependenceDevelopmentDiploid CellsDisciplineDiseaseElementsExplosionFour-dimensionalFundingGasesGene ExpressionGenesGenomeGenomicsGenotypeGoalsHumanHuman Genome ProjectIndividualKnowledgeLaboratoriesLeadLinear RegressionsLinkLiquid substanceLiteratureMapsMeasuresMentorsModelingMolecular BiologyMolecular ProfilingNational Human Genome Research InstituteOncogenic VirusesOncornavirusesPathway interactionsPharmaceutical PreparationsPhase TransitionPhenotypePhysicsPopulationPositioning AttributeProcessPropertyRNA InterferenceRecording of previous eventsResearchRoleScienceSecureSolidSourceSystemSystems BiologyTechnologyTemperatureTestingTherapeuticThermodynamicsTimeTissuesTrainingTraining ProgramsViralViral ProteinsVirusWaterWorkWrestlingbasebiological systemscareer developmentcell growthgene interactionhuman diseaseinsightmathematical modelmeetingsmetaplastic cell transformationmigrationnetwork modelsnovelpredictive modelingpressureprogramsprotein protein interactionresearch studyresponsesimulationstatisticstheoriestranscription factor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): One of the greatest challenges in modern biomedical research is to understand the link between genotype and phenotype and, more importantly, to create models that allow us to predict the response of biological systems to various perturbations that can affect them. Despite an explosion of data that has emerged from genomic technologies, and continued efforts to develop models that capture the complexity of biological systems, we have not yet made significant progress in achieving these goals. Here we propose to develop new, phenomenological approaches that leverage empirical data together with information from other sources such as the biomedical literature, to create predictive models that can be further tested and validated. To understand the global properties of transcriptional networks and to predict the elements with the greatest potential to effect phenotypic changes, we will map our models to thermodynamic spin systems which allow us to identify robust gene modules and associated order parameters. We hypothesize that these order parameters drive phenotypic transitions in a manner analogous to the pressure and temperature dependent phase transitions of water between solid, liquid and gas. To develop and test this approach, we will use data currently being generated through the NHGRI-funded Center for Excellence in Genome Science (CEGS) program in which we are investigating the mechanisms by which oncovirus-derived genes perturb cellular networks to drive cellular transformation. The modules we identify will be used to make concrete predictions about key parameters essential for transformation and these predictions will be tested by using RNAi to perturb the cellular networks and evaluating the response by gene expression analysis and phenotypic assays. Working with my mentor, Dr. John Quackenbush, and co-mentors, Dr. Karl Munger and Dr. Giovanni Parmigiani, this project will allow me to develop a research program that will facilitate my transition from physics to biology and help me to secure an independent research position. To further support my career development, my mentors and I have developed a rigorous training program that will provide me with formal training in statistics and computational biology, and hands-on training in modern laboratory molecular biology.
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依托单位:
海外基金