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Comparative Methods for Gene Structure Prediction in Homologous Sequences

机译:同源序列中基因结构预测的比较方法

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The increasing number of sequenced genomes motivates the use of evolutionary patterns to detect genes. We present a series of comparative methods for gene finding in homologous prokaryotic or eukary-otic sequences. Based on a model of legal genes and a similarity measure between genes, we find the pair of legal genes of maximum similarity. We develop methods based on genes models and alignment based similarity measures of increasing complexity, which take into account many details of real gene structures, e.g. the similarity of the proteins encoded by the exons. When using a similarity measure based on an exiting alignment, the methods run in linear time. When integrating the alignment and prediction process which allows for more fine grained similarity measures, the methods run in quadratic time. We evaluate the methods in a series of experiments on synthetic and real sequence data, which show that all methods are competitive but that taking the similarity of the encoded proteins into account really boost the performance.
机译:越来越多的测序基因组促使人们使用进化模式来检测基因。我们提出了在原核或真核同源序列中寻找基因的一系列比较方法。基于合法基因的模型和基因之间的相似性度量,我们找到了一对具有最大相似性的合法基因。我们开发了基于基因模型和基于比对的相似性度量的方法,这些方法增加了复杂性,其中考虑了真实基因结构的许多细节,例如外显子编码的蛋白质的相似性。当使用基于现有比对的相似性度量时,这些方法以线性时间运行。当整合对齐和预测过程以实现更细粒度的相似性度量时,这些方法将以二次时间运行。我们在合成和真实序列数据的一系列实验中评估了这些方法,这些方法表明所有方法都具有竞争性,但是考虑编码蛋白的相似性确实可以提高性能。

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