特异性和群体约束下的结构一致基序推理新方法

Christine Sinoquet
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引用次数: 0

摘要

我们解决了结构化基序推理的问题。这个问题的描述如下:给定一组n个DNA序列和一个quorum q(%),找到最优的结构共识基序,该基序被描述为与特定区域交替的间隙,并且至少被qxn个序列共享。我们的建议是在元启发式领域:它通过搜索空间的采样策略和小序列样本的局部相似性的快速检测之间的合作来运行收敛的解决方案。本文的贡献有:(1)设计了一种随机方法,其真正的新颖性在于用区分特定区域和间隙的阈值频率f驱动搜索;(二)特别设计的作业的原有论证方式;(3)实现了一种适合生物学家需求的挖掘工具:需要很少的输入参数(quorum q,最小阈值频率f,最大间隙长度g)。我们的方法在模拟数据,Dicot植物的启动子位点和大肠杆菌基因组的转录因子结合位点上证明是有效的。我们的算法Kaos在准确率上优于MEME和STARS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel Approach for Structured Consensus Motif Inference Under Specificity and Quorum Constraints
We address the issue of structured motif inference. This problem is stated as follows: given a set of n DNA sequences and a quorum q (%), find the optimal structured consensus motif described as gaps alternating with specific regions and shared by at least q x n sequences. Our proposal is in the domain of metaheuristics: it runs solutions to convergence through a cooperation between a sampling strategy of the search space and a quick detection of local similarities in small sequence samples. The contributions of this paper are: (1) the design of a stochastic method whose genuine novelty rests on driving the search with a threshold frequency f discrimining between specific regions and gaps; (2) the original way for justifying the operations especially designed; (3) the implementation of a mining tool well adapted to biologists' exigencies: few input parameters are required (quorum q, minimal threshold frequency f, maximal gap length g). Our approach proves efficient on simulated data, promoter sites in Dicot plants and transcription factor binding sites in E. coli genome. Our algorithm, Kaos, compares favorably with MEME and STARS in terms of accuracy.
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