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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.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1371/journal.pcbi.1001106
发表时间: 2011-06
期刊: PLoS computational biology
影响因子: 4.3
作者: [Li W, Liu CC, Zhang T, Li H, Waterman MS, Zhou XJ]
通讯作者: Zhou XJ
DOI: 10.1016/j.arr.2009.10.006
发表时间: 2010-07
期刊: AGEING RESEARCH REVIEWS
影响因子: 13.1
作者: [de Magalhaes, Joao Pedro, Finch, Caleb E., Janssens, Georges]
通讯作者: Janssens, Georges
Unraveling complex temporal associations in cellular systems across multiple time-series microarray datasets.
跨多个时间序列微阵列数据集揭示细胞系统中复杂的时间关联。
DOI: 10.1016/j.jbi.2009.12.006
发表时间: 2010
期刊: Journal of biomedical informatics
影响因子: 4.5
作者: [Li,Wenyuan, Xu,Min, Zhou,XianghongJasmine]
通讯作者: Zhou,XianghongJasmine
Detecting and locating cancer for patients with CT-detected lung nodules
Detecting and locating cancer for patients with CT-detected lung nodules
Integrative Analysis of Public RNA-seq Repositories
  • 批准号:
    8470017
  • 项目类别:
  • 资助金额:
    $32.45万
  • 财政年份:
    2013
  • 负责人:
    XIANGHONG Jasmine ZHOU
  • 依托单位:
Integrative Analysis of Public RNA-seq Repositories
  • 批准号:
    8637092
  • 项目类别:
  • 资助金额:
    $30.89万
  • 财政年份:
    2013
  • 负责人:
    XIANGHONG Jasmine ZHOU
  • 依托单位:
国内基金
海外基金
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
  • 批准号:
    JCZRQN202500010
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
  • 依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
  • 批准号:
    2025JJ70209
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    雷芬芳
  • 依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
  • 批准号:
    --
  • 项目类别:
    面上项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    万荣
  • 依托单位: