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Comparative Methods for Gene Structure Prediction in Homologous Sequences

机译:同源序列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 eukaryotic 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使用进化模式来检测基因。我们提出了一系列比较方法在同源原核或真核序列中发现基因。基于法律基因的模型和基因之间的相似性测量,我们发现了一对最大相似性的法律基因。我们基于基因模型的发展方法和基于对准的复杂性的对准相似度测量,这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。使用基于退出对齐的相似度量时,该方法在线性时间运行。当集成允许更细粒度相似度测量的对准和预测过程时,该方法在二次时间中运行。我们评估了一系列关于合成和实际序列数据的一系列实验中的方法,表明所有方法都具有竞争力,而是考虑编码蛋白的相似性真正提高了性能。

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