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Cyclebase.org:版本 2.0,一个经过更新的全面的、多物种的细胞周期实验和衍生分析结果资源库。

Cyclebase.org: version 2.0, an updated comprehensive, multi-species repository of cell cycle experiments and derived analysis results.

机构信息

Computational Biology Center, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA.

出版信息

Nucleic Acids Res. 2010 Jan;38(Database issue):D699-702. doi: 10.1093/nar/gkp1044. Epub 2009 Nov 24.

Abstract

Cell division involves a complex series of events orchestrated by thousands of molecules. To study this process, researchers have employed mRNA expression profiling of synchronously growing cell cultures progressing through the cell cycle. These experiments, which have been carried out in several organisms, are not easy to access, combine and evaluate. Complicating factors include variation in interdivision time between experiments and differences in relative duration of each cell-cycle phase across organisms. To address these problems, we created Cyclebase, an online resource of cell-cycle-related experiments. This database provides an easy-to-use web interface that facilitates visualization and download of genome-wide cell-cycle data and analysis results. Data from different experiments are normalized to a common timescale and are complimented with key cell-cycle information and derived analysis results. In Cyclebase version 2.0, we have updated the entire database to reflect changes to genome annotations, included information on cyclin-dependent kinase (CDK) substrates, predicted degradation signals and loss-of-function phenotypes from genome-wide screens. The web interface has been improved and provides a single, gene-centric graph summarizing the available cell-cycle experiments. Finally, key information and links to orthologous and paralogous genes are now included to further facilitate comparison of cell-cycle regulation across species. Cyclebase version 2.0 is available at http://www.cyclebase.org.

摘要

细胞分裂涉及由数千个分子精心策划的复杂事件序列。为了研究这个过程,研究人员采用了对同步生长的细胞培养物进行 mRNA 表达谱分析的方法,这些细胞培养物正在经历细胞周期。这些在几个生物体中进行的实验不容易获取、组合和评估。复杂的因素包括实验之间的细胞分裂时间的变化以及不同生物体中每个细胞周期阶段的相对持续时间的差异。为了解决这些问题,我们创建了在线细胞周期相关实验资源 Cyclebase。这个数据库提供了一个易于使用的 Web 界面,方便对全基因组细胞周期数据和分析结果进行可视化和下载。来自不同实验的数据被归一化为共同的时间尺度,并附有关键的细胞周期信息和衍生的分析结果。在 Cyclebase 2.0 版本中,我们更新了整个数据库,以反映基因组注释的变化,包括来自全基因组筛选的细胞周期蛋白依赖性激酶 (CDK) 底物、预测的降解信号和功能丧失表型的信息。Web 界面得到了改进,并提供了一个单一的、以基因为中心的图表,总结了可用的细胞周期实验。最后,现在包括了关键信息和同源及直系同源基因的链接,以进一步促进跨物种的细胞周期调控比较。Cyclebase 2.0 版本可在 http://www.cyclebase.org 获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894b/2808877/7073f57890db/gkp1044f1.jpg

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