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Model-based prediction of sequence alignment quality

机译:基于模型的序列比对质量预测

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Motivation: Multiple sequence alignment (MSA) is an essential prerequisite for many sequence analysis methods and valuable tool itself for describing relationships between protein sequences. Since the success of the sequence analysis is highly dependent on the reliability of alignments, measures for assessing the quality of alignments are highly requisite.Results: We present a statistical model-based alignment quality score. Unlike other quality scores, it does not require several parallel alignments for the same set of sequences or additional structural information. Our quality score is based on measuring the conservation level of reference alignments in Homstrad. Reference sequences were realigned with the Mafft, Muscle and Probcons alignment programs, and a sum-of-pairs (SP) score was used to measure the quality of the realignments. Statistical modelling of the SP score as a function of conservation level and other alignment characteristics makes it possible to predict the SP score for any global MSA. The predicted SP scores are highly correlated with the correct SP scores, when tested on the Homstrad and SABmark databases. The results are comparable to that of multiple overlap score (MOS) and better than those of normalized mean distance (NorMD) and normalized iRMSD (NiRMSD) alignment quality criteria. Furthermore, the predicted SP score is able to detect alignments with badly aligned or unrelated sequences.
机译:动机:多重序列比对(MSA)是许多序列分析方法和描述蛋白质序列之间关系的重要工具本身的必要前提。由于序列分析的成功高度依赖于比对的可靠性,因此评估比对质量的措施非常必要。结果:我们提出了一种基于统计模型的比对质量评分。与其他质量得分不同,对于同一序列集或其他结构信息,它不需要几次平行比对。我们的质量得分是基于对Homstrad中参照比对的保守性水平进行测量的。将参考序列与Mafft,Muscle和Probcons比对程序重新比对,并且使用成对和(SP)评分来衡量重新比对的质量。 SP得分作为保护水平和其他比对特征的函数的统计模型使得可以预测任何全局MSA的SP得分。在Homstrad和SABmark数据库上进行测试时,预测的SP得分与正确的SP得分高度相关。结果与多重重叠评分(MOS)相当,并且优于归一化平均距离(NorMD)和归一化iRMSD(NiRMSD)对齐质量标准的结果。此外,预测的SP得分能够检测序列比对不良或不相关的比对。

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