A Community Effort to Translate Protein Data to Knowledge: An Integrated Platform
A Community Effort to Translate Protein Data to Knowledge: An Integrated Platform
批准号:
9298691
负责人:
MERRY L LINDSEY
金额:
$457.84万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-09-29 至 2019-04-30
关键词:
AchievementAddressAlgorithmic SoftwareAlgorithmsArchitectureAwarenessBig DataBig Data to KnowledgeBioinformaticsBiologicalCardiovascular DiseasesCardiovascular systemClinicalClinical DataCloud ComputingCommunitiesComputational BiologyDataData AnalysesData ScienceData SetDimensionsDiseaseEducation and OutreachElderlyEnvironmentExhibitsFaceFundingFutureGene ProteinsGeneral PopulationGenerationsGenesGoalsHalf-LifeHarvestHealthHumanImageryIntuitionJackson Heart StudyKnowledgeLiteratureLongevityMachine LearningMapsMedicineMiningModelingModernizationModificationMolecularMolecular ProfilingMolecular StructureOrganPathway interactionsPatientsPharmaceutical PreparationsPhenotypePhysiologicalPopulation ResearchPropertyProtein AnalysisProtein DynamicsProteinsRecording of previous eventsResearchResearch PersonnelResearch ProposalsResourcesRestScientistStructureSystemTimeTrainingTraining and EducationTranscriptTranslatingUnited States National Institutes of Healthbig biomedical dataclinical phenotypeclinical predictorscohortcomputerized data processingcomputerized toolscrowdsourcingdata managementdata miningdata modelingdata resourcedata to knowledgedesignexperienceimprovedinnovationinsightinterestlearning strategymolecular scalemultiple omicsnoveloperationoutreach programprotein complexprotein expressionprotein metaboliteprotein protein interactionpublic health relevancerepositoryspatiotemporalsuccesssupport toolstext searchingtool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The inception of the BD2K Initiative is a testament to the foresight of NIH and our community. Clearly, the future of biomedicine rests on our collective ability to transform Big Data into intelligible scientific facts. In line with the BD2K objectives,our goal is to revolutionize how we address the universal challenge to discern meaning from unruly data. Capitalizing on our investigators' complementary strengths in computational biology and cardiovascular medicine, we will present a fusion of cutting-edge innovations that are grounded in a cardiovascular research focus, encompassing: (i) on-the-cloud data processing, (ii) crowd sourcing and text-mining data annotation, (iii) protein spatiotemporal dynamics, (iv) multi-omic integration, and (v) multiscale clinical data modeling. Drawing from our decade of experience in creating and refining bioinformatics tools, we propose to amalgamate established Big Data resources into a generalizable model for data annotation and collaborative research, through a new query system and cloud infrastructure for accessing multiple omics repositories, and through computational-supported crowdsourcing initiatives for mining the biomedical literature. We propose to interweave diverse data types for revealing biological networks that coalesce from molecular entities at multiple scales, through machine learning methods for structuring molecular data and defining relationships with drugs and diseases, and through novel algorithms for on-the-cloud integration and pathway visualization of multi-dimensional molecular data. Moreover, we propose to innovate advanced modeling tools to resolve protein dynamics and spatiotemporal molecular mechanisms, through mechanistic modeling of protein properties and 3D protein expression maps, and through Bayesian algorithms that correlate patient phenotypes, health histories, and multi-scale molecular profiles. The utility and customizability o our tools to the broader research population is clearly demonstrated using three archetypical workflows that enable annotations of large lists of genes, transcripts, proteins, or metabolites; powerful analysis of complex protein datasets acquired over time; and seamless aQoregation of diverse molecular, textual and literature data. These workflows will be rigorously validated using data from two significant clinical cohorts, the Jackson Heart Study and the Healthy Elderly Longevity (Wellderly). In parallel, a multifaceted strategy will be implemented to educate and train biomedical investigators, and to engage the public for promoting the overall BD2K initiative.
We are convinced that a community-driven BD2K initiative will best realize its scientific potential
and transform the research culture in a sustainable manner, exhibiting lasting success beyond the current funding period.
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DOI:
10.1016/j.gene.2015.08.062
发表时间:
2015-12-01
期刊:
Gene
影响因子:
3.5
作者:
[Veerman CC, Wilde AA, Lodder EM]
通讯作者:
Lodder EM
Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy.
线粒体载体转位酶通道亚基 TIM22 的突变会导致早发性线粒体肌病。
DOI:
10.1093/hmg/ddy305
发表时间:
2018
期刊:
Human molecular genetics
影响因子:
3.5
作者:
[Pacheu-Grau,David, Callegari,Sylvie, Emperador,Sonia, Thompson,Kyle, Aich,Abhishek, Topol,SarahE, Spencer,EmilyG, McFarland,Robert, Ruiz-Pesini,Eduardo, Torkamani,Ali, Taylor,RobertW, Montoya,Julio, Rehling,Peter]
通讯作者:
Rehling,Peter
DOI:
10.1016/j.gene.2016.07.070
发表时间:
2016-10-30
期刊:
Gene
影响因子:
3.5
作者:
[Hubacek JA]
通讯作者:
Hubacek JA
DOI:
10.1016/j.gene.2015.09.008
发表时间:
2015-12-01
期刊:
Gene
影响因子:
3.5
作者:
[Carrier L, Mearini G, Stathopoulou K, Cuello F]
通讯作者:
Cuello F
DOI:
10.1016/j.gene.2015.09.029
发表时间:
2016-01-10
期刊:
Gene
影响因子:
3.5
作者:
[Sugawara K, Shibasaki T, Takahashi H, Seino S]
通讯作者:
Seino S
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A Community Effort to Translate Protein Data to Knowledge: An Integrated Platform
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Neutrophil Polarization Following Myocardial Infarction
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MMP-9 Roles in the Aging Myocardial Response to Ischemia
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