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在一个集成框架中对基序发现方法的调查。

A survey of motif discovery methods in an integrated framework.

作者信息

Sandve Geir Kjetil, Drabløs Finn

机构信息

Department of Computer and Information Science, NTNU - Norwegian University of Science and Technology, N-7052, Trondheim, Norway.

出版信息

Biol Direct. 2006 Apr 6;1:11. doi: 10.1186/1745-6150-1-11.

Abstract

BACKGROUND

There has been a growing interest in computational discovery of regulatory elements, and a multitude of motif discovery methods have been proposed. Computational motif discovery has been used with some success in simple organisms like yeast. However, as we move to higher organisms with more complex genomes, more sensitive methods are needed. Several recent methods try to integrate additional sources of information, including microarray experiments (gene expression and ChlP-chip). There is also a growing awareness that regulatory elements work in combination, and that this combinatorial behavior must be modeled for successful motif discovery. However, the multitude of methods and approaches makes it difficult to get a good understanding of the current status of the field.

RESULTS

This paper presents a survey of methods for motif discovery in DNA, based on a structured and well defined framework that integrates all relevant elements. Existing methods are discussed according to this framework.

CONCLUSION

The survey shows that although no single method takes all relevant elements into consideration, a very large number of different models treating the various elements separately have been tried. Very often the choices that have been made are not explicitly stated, making it difficult to compare different implementations. Also, the tests that have been used are often not comparable. Therefore, a stringent framework and improved test methods are needed to evaluate the different approaches in order to conclude which ones are most promising.

REVIEWERS

This article was reviewed by Eugene V. Koonin, Philipp Bucher (nominated by Mikhail Gelfand) and Frank Eisenhaber.

摘要

背景

对调控元件的计算发现的兴趣日益浓厚,并且已经提出了众多基序发现方法。计算基序发现在酵母等简单生物体中已取得一定成功。然而,随着我们转向基因组更复杂的高等生物体,需要更灵敏的方法。最近的几种方法试图整合包括微阵列实验(基因表达和芯片杂交)在内的其他信息来源。人们也越来越意识到调控元件是协同起作用的,并且这种组合行为必须被建模才能成功进行基序发现。然而,方法和途径众多,难以很好地了解该领域的现状。

结果

本文基于一个整合了所有相关要素的结构化且定义明确的框架,对DNA中的基序发现方法进行了综述。根据该框架对现有方法进行了讨论。

结论

综述表明,尽管没有单一方法考虑到所有相关要素,但已经尝试了大量分别处理各种要素的不同模型。所做的选择往往没有明确说明,这使得难以比较不同的实现方式。此外,所使用的测试通常也不可比。因此,需要一个严格的框架和改进的测试方法来评估不同的方法,以便确定哪些方法最有前景。

评审人

本文由尤金·V·库宁、菲利普·布赫尔(由米哈伊尔·格尔凡德提名)和弗兰克·艾森哈伯评审。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aaa/1479319/cbe3c41d140c/1745-6150-1-11-1.jpg

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