Scalable Convex Multiple Sequence Alignment via Entropy-Regularized Dual Decomposition.

Jiong Zhang, Ian E H Yen, Pradeep Ravikumar, Inderjit S Dhillon
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Abstract

Multiple Sequence Alignment (MSA) is one of the fundamental tasks in biological sequence analysis that underlies applications such as phylogenetic trees, profiles, and structure prediction. The task, however, is NP-hard, and the current practice resorts to heuristic and local-search methods. Recently, a convex optimization approach for MSA was proposed based on the concept of atomic norm [23], which demonstrates significant improvement over existing methods in the quality of alignments. However, the convex program is challenging to solve due to the constraint given by the intersection of two atomic-norm balls, for which the existing algorithm can only handle sequences of length up to 50, with an iteration complexity subject to constants of unknown relation to the natural parameters of MSA. In this work, we propose an accelerated dual decomposition algorithm that exploits entropy regularization to induce closed-form solutions for each atomic-norm-constrained subproblem, giving a single-loop algorithm of iteration complexity linear to the problem size (total length of all sequences). The proposed algorithm gives significantly better alignments than existing methods on sequences of length up to hundreds, where the existing convex programming method fails to converge in one day.

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基于熵正则化对偶分解的可伸缩凸多序列对齐。
多序列比对(MSA)是生物序列分析的基础任务之一,是系统发育树、基因图谱和结构预测等应用的基础。然而,这项任务是np困难的,目前的实践采用启发式和局部搜索方法。最近,一种基于原子范数概念的MSA凸优化方法被提出[23],该方法在对齐质量上比现有方法有了显著提高。然而,由于两个原子范数球相交的约束,现有算法只能处理长度不超过50的序列,且迭代复杂度受与MSA自然参数关系未知的常数的影响,使得凸规划的求解具有挑战性。在这项工作中,我们提出了一种加速的对偶分解算法,该算法利用熵正则化来诱导每个原子规范约束子问题的封闭形式解,给出了迭代复杂度与问题大小(所有序列的总长度)线性的单环算法。对于长度达数百的序列,该算法比现有的凸规划方法在一天内不能收敛的情况下具有更好的对齐效果。
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