RNA伪结折叠动态规划方案的自动设计。

IF 1.5 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS Algorithms for Molecular Biology Pub Date : 2023-12-01 DOI:10.1186/s13015-023-00229-z
Bertrand Marchand, Sebastian Will, Sarah J Berkemer, Yann Ponty, Laurent Bulteau
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引用次数: 1

摘要

虽然RNA二级结构预测是动态规划(DP)的教科书应用和RNA结构分析的常规任务,但每当假结发挥作用时,它仍然具有挑战性。由于通过最小化(实际建模)能量来预测伪结结构是np困难的,因此已经提出了用于捕获最常观察到的构型的受限构象类的专门算法。为了获得良好的性能,这些方法依赖于特定的、精心制作的DP方案。相反,我们推广和完全自动化了DP伪结预测算法的设计。为此,我们形式化了为(无限)类构象设计DP算法的问题,由(有限数量)图形建模,并自动构建最小化其算法复杂性的DP方案。我们提出了一个算法来解决这个问题,基于一个精心选择的代表性结构的树分解,我们将其简化并重新解释为一个DP方案。对于脂肪图的树宽tw,该算法是固定参数可处理的,其输出表示用于预测长度为n的RNA的MFE折叠的[公式:参见文本]算法(甚至可能在简单能量模型中[公式:参见文本])。我们证明,对于最常见的伪结类,我们自动生成的算法实现了与文献中报道的手工方案相同的复杂性。我们的框架支持一般的能量模型、配分函数计算、递归子结构和部分折叠,并且可以为超越上下文无关情况的代数动态规划铺平道路。
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Automated design of dynamic programming schemes for RNA folding with pseudoknots.

Although RNA secondary structure prediction is a textbook application of dynamic programming (DP) and routine task in RNA structure analysis, it remains challenging whenever pseudoknots come into play. Since the prediction of pseudoknotted structures by minimizing (realistically modelled) energy is NP-hard, specialized algorithms have been proposed for restricted conformation classes that capture the most frequently observed configurations. To achieve good performance, these methods rely on specific and carefully hand-crafted DP schemes. In contrast, we generalize and fully automatize the design of DP pseudoknot prediction algorithms. For this purpose, we formalize the problem of designing DP algorithms for an (infinite) class of conformations, modeled by (a finite number of) fatgraphs, and automatically build DP schemes minimizing their algorithmic complexity. We propose an algorithm for the problem, based on the tree-decomposition of a well-chosen representative structure, which we simplify and reinterpret as a DP scheme. The algorithm is fixed-parameter tractable for the treewidth tw of the fatgraph, and its output represents a [Formula: see text] algorithm (and even possibly [Formula: see text] in simple energy models) for predicting the MFE folding of an RNA of length n. We demonstrate, for the most common pseudoknot classes, that our automatically generated algorithms achieve the same complexities as reported in the literature for hand-crafted schemes. Our framework supports general energy models, partition function computations, recursive substructures and partial folding, and could pave the way for algebraic dynamic programming beyond the context-free case.

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来源期刊
Algorithms for Molecular Biology
Algorithms for Molecular Biology 生物-生化研究方法
CiteScore
2.40
自引率
10.00%
发文量
16
审稿时长
>12 weeks
期刊介绍: Algorithms for Molecular Biology publishes articles on novel algorithms for biological sequence and structure analysis, phylogeny reconstruction, and combinatorial algorithms and machine learning. Areas of interest include but are not limited to: algorithms for RNA and protein structure analysis, gene prediction and genome analysis, comparative sequence analysis and alignment, phylogeny, gene expression, machine learning, and combinatorial algorithms. Where appropriate, manuscripts should describe applications to real-world data. However, pure algorithm papers are also welcome if future applications to biological data are to be expected, or if they address complexity or approximation issues of novel computational problems in molecular biology. Articles about novel software tools will be considered for publication if they contain some algorithmically interesting aspects.
期刊最新文献
On the parameterized complexity of the median and closest problems under some permutation metrics. TINNiK: inference of the tree of blobs of a species network under the coalescent model. New generalized metric based on branch length distance to compare B cell lineage trees. Metric multidimensional scaling for large single-cell datasets using neural networks. Compression algorithm for colored de Bruijn graphs.
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