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Model-based methods for identifying periodically expressed genes based on time course microarray gene expression data

机译:基于时程微阵列基因表达数据的周期性表达基因识别的基于模型的方法

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Motivation: The expressions of many genes associated with certain periodic biological and cell cycle processes such as circadian rhythm regulation are known to be rhythmic. Identification of the genes whose time course expressions are synchronized to certain periodic biological process may help to elucidate the molecular basis of many diseases, and these gene products may in turn represent drug targets relevant to those diseases. Results: We propose in this paper a statistical framework based on a shape-invariant model together with a false discovery rate (FDR) procedure for identifying periodically expressed genes based on microarray time-course gene expression data and a set of known periodically expressed guide genes. We applied the proposed methods to the -factor, cdc15 and cdc28 synchronized yeast cell cycle data sets and identified a total of 1010 cell-cycle-regulated genes at a FDR of 0.5% in at least one of the three data sets analyzed, including 89 (86%) of 104 known periodic transcripts. We also identified 344 and 201 circadian rhythmic genes in vivo in mouse heart and liver tissues with FDR of 10 and 2.5%, respectively. Our results also indicate that the shape-invariant model fits the data well and provides estimate of the common shape function and the relative phases for these periodically regulated genes.
机译:动机:许多与某些周期性生物学和细胞周期过程(例如昼夜节律调节)相关的基因的表达具有节律性。鉴定其时程表达与某些周期性生物学过程同步的基因可能有助于阐明许多疾病的分子基础,而这些基因产物又可以代表与那些疾病相关的药物靶标。结果:我们在本文中提出了一个基于形状不变模型的统计框架,以及基于微阵列时程基因表达数据和一组已知的周期性表达的指导基因来鉴定周期性表达的基因的错误发现率(FDR)程序。 。我们将拟议的方法应用于-factor,cdc15和cdc28同步酵母细胞周期数据集,并在至少三个分析的数据集中之一中,以0.5%的FDR鉴定了总共1010个细胞周期调控的基因,其中包括89个(104%)的已知周期性笔录(86%)。我们还确定了小鼠心脏和肝脏组织中的344和201昼夜节律基因在体内,FDR分别为10%和2.5%。我们的结果还表明,形状不变模型很好地拟合了数据,并为这些周期性调节的基因提供了通用形状函数和相对相位的估计。

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