基于改进预处理和反对称计算模型的串联质谱多肽测序算法。

K. Ning, H. Leong
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引用次数: 10

摘要

肽段串联质谱测序是蛋白质组学中一个非常重要、有趣但又具有挑战性的问题。近年来,这一问题得到了研究人员的广泛研究,肽测序结果也越来越准确。然而,这些算法中的许多都使用基于一些未经验证的假设的计算模型。我们相信,对这些假设和相关问题的有效性的调查将导致当前算法的改进。在本文中,我们首次研究了不经谱预处理的多肽测序,并证明了在谱上引入预处理可以使多肽测序更快、更容易、更准确。然后,我们研究了一个非常重要的问题,即肽序列问题中的反对称问题,并通过实验证明,对于肽序列问题,简单地忽略模型的反对称,去掉所有反对称实例的模型过于简单。我们提出了一种更现实的反对称问题的新模型。我们还提出了一种新的算法,该算法结合了预处理和新的模型来处理反对称问题,实验表明该算法在检验的数据集上具有更好的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Algorithm for peptide sequencing by tandem mass spectrometry based on better preprocessing and anti-symmetric computational model.
Peptide sequencing by tandem mass spectrometry is a very important, interesting, yet challenging problem in proteomics. This problem is extensively investigated by researchers recently, and the peptide sequencing results are becoming more and more accurate. However, many of these algorithms are using computational models based on some unverified assumptions. We believe that the investigation of the validity of these assumptions and related problems will lead to improvements in current algorithms. In this paper, we have first investigated peptide sequencing without preprocessing the spectrum, and we have shown that by introducing preprocessing on spectrum, peptide sequencing can be faster, easier and more accurate. We have then investigated one very important problem, the anti-symmetric problem in the peptide sequencing problem, and we have proved by experiments that model that simply ignore anti-symmetric of model that remove all anti-symmetric instances are too simple for peptide sequencing problem. We have proposed a new model for anti-symmetric problem in more realistic way. We have also proposed a novel algorithm which incorporate preprocessing and new model for anti-symmetric issue, and experiments show that this algorithm has better performance on datasets examined.
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