A web platform for integrative genomic analysis in aging
A web platform for integrative genomic analysis in aging
批准号:
7432003
负责人:
XIANGHONG Jasmine ZHOU
金额:
$20.05万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-03-01 至 2010-02-28
关键词:
AddressAgeAgingAllyAnimal ModelAtlasesBioinformaticsBiologicalBiological ProcessCaenorhabditis elegansCell Differentiation processChronic DiseaseCommunitiesConditionDataData SetData SourcesDatabasesDepositionDevelopmentFacility Construction Funding CategoryGap JunctionsGene ExpressionGenesGeneticGenomeGenomicsHumanInflammatoryInternetKnowledgeLaboratoriesLinkLiteratureMalignant NeoplasmsMeasurementMeasuresMethodsMicroarray AnalysisMiningModelingMusNexus (resin cement)NumbersOrganismPathway interactionsPatternPhaseRattusRecurrenceReportingResearchResourcesSaccharomyces cerevisiaeSignal TransductionSystemTissuesTranscription Regulation PathwayTranscriptional RegulationVascular DiseasesWorkYeastsage relatedaging genebasedata integrationdesigngenome sequencinghigh throughput technologyimprovednovelprotein protein interactionresearch studytooluser-friendlyweb interface
中文摘要
描述(由申请人提供):最近高通量技术的发展产生了大量的基因组数据,以了解衰老的遗传基础。例如,80多项微阵列研究直接解决了不同模式生物和不同条件下与衰老相关的表达模式。然而,由于缺乏生物信息学资源来方便地跨实验室搜索主阵列信号,对大量微阵列数据的有效利用受到阻碍。我们开发了网络数据库Gene Aging Nexus (GAN),供生物老年病研究界免费访问,以查询/分析/可视化各种与衰老相关的基因组数据源,特别是微阵列数据。在本提案中,我们将继续GAN的开发。具体而言,(1)我们将扩展中央网络数据库,以获取六种物种的衰老微阵列数据:人类(H. sapiens)、大鼠(R. norvegicus)、小鼠(M. musculus)、苍蝇(D. melanogaster)、蠕虫(C. elegans)和酵母(S. cerevisiae)。(2)我们将实现一套用于跨平台微阵列数据集成和分析的新工具,并实现文献中报道的有用方法。(3)我们将整合其他基因组数据来源,如生物学途径、转录调控、蛋白质-蛋白质相互作用、基因组序列和文献知识。通过整合这些数据,用户将能够更好地理解和解释来自阵列分析的结果,将未知基因分配到与衰老相关的途径,并预测转录调控。GAN可以帮助启动下一阶段,评估不同生物组织中衰老相关基因表达的可能共性。
英文摘要
DESCRIPTION (provided by applicant): The recent development of high-throughput technologies generated enormous genomic data to understand the genetic basis of aging. For example, more than eighty microarray studies have directly addressed aging-related expression patterns in diverse model organisms and under different conditions. However, efficient exploitation of this vast amount of microarray data is frustrated by the lack of bioinformatics resources to enable convenient cross-laboratory searches of primary array signals. We have develop the web-database Gene Aging Nexus (GAN) freely accessible to the biogerontological-geriatric research community to query/analyze/visualize various aging-related genomic data sources, in particular, microarray data. In this proposal, we will continue the development of GAN. In particular, (1) We will expand the central web database for aging microarray data of six species: human (H. sapiens), rat (R. norvegicus), mouse (M. musculus), `fly' (D. melanogaster), `worm' (C. elegans), and yeast (S. cerevisiae). (2) We will implement a set of novel tools for cross-platform microarray data integration and analysis, and also implement useful methods reported in the literature. (3) We will incorporate other genomic data sources, such as biological pathways, transcription regulation, protein-protein interactions, genome sequences, and literature knowledge. By integrating such data, users will be able to better understand and interpret the results derived from array analysis, to assign unknown genes to aging-related pathways, and to predict transcriptional regulation. GAN could help launch the next phase of evaluating possible universals in aging-related gene expression in tissues of diverse organisms.
The construction of the GAN platform and the associated analysis of a large number of public aging genomic data could constitute one of the largest bioinformatics undertakings in aging research. GAN could help launch the next phase of evaluating possible universals in aging-related gene expression in tissues of diverse organisms, and facilitates the systems understanding of aging.
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