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MAFFT多序列比对程序的最新进展。

Recent developments in the MAFFT multiple sequence alignment program.

作者信息

Katoh Kazutaka, Toh Hiroyuki

机构信息

Digital Medicine Initiative, Kyushu University, Fukuoka 812-8582, Japan.

出版信息

Brief Bioinform. 2008 Jul;9(4):286-98. doi: 10.1093/bib/bbn013. Epub 2008 Mar 27.

Abstract

The accuracy and scalability of multiple sequence alignment (MSA) of DNAs and proteins have long been and are still important issues in bioinformatics. To rapidly construct a reasonable MSA, we developed the initial version of the MAFFT program in 2002. MSA software is now facing greater challenges in both scalability and accuracy than those of 5 years ago. As increasing amounts of sequence data are being generated by large-scale sequencing projects, scalability is now critical in many situations. The requirement of accuracy has also entered a new stage since the discovery of functional noncoding RNAs (ncRNAs); the secondary structure should be considered for constructing a high-quality alignment of distantly related ncRNAs. To deal with these problems, in 2007, we updated MAFFT to Version 6 with two new techniques: the PartTree algorithm and the Four-way consistency objective function. The former improved the scalability of progressive alignment and the latter improved the accuracy of ncRNA alignment. We review these and other techniques that MAFFT uses and suggest possible future directions of MSA software as a basis of comparative analyses. MAFFT is available at http://align.bmr.kyushu-u.ac.jp/mafft/software/.

摘要

DNA和蛋白质的多序列比对(MSA)的准确性和可扩展性长期以来一直是且仍然是生物信息学中的重要问题。为了快速构建合理的MSA,我们在2002年开发了MAFFT程序的初始版本。如今,MSA软件在可扩展性和准确性方面面临着比5年前更大的挑战。随着大规模测序项目产生越来越多的序列数据,可扩展性在许多情况下变得至关重要。自从发现功能性非编码RNA(ncRNA)以来,准确性的要求也进入了一个新阶段;在构建远缘相关ncRNA的高质量比对时应考虑二级结构。为了解决这些问题,2007年我们用两种新技术将MAFFT更新到了版本6:PartTree算法和四路一致性目标函数。前者提高了渐进比对的可扩展性,后者提高了ncRNA比对的准确性。我们回顾了MAFFT使用的这些以及其他技术,并作为比较分析的基础提出了MSA软件未来可能的发展方向。可在http://align.bmr.kyushu-u.ac.jp/mafft/software/获取MAFFT。

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