成对比较
计算机科学
多序列比对
隐马尔可夫模型
Python(编程语言)
序列比对
水准点(测量)
支持向量机
数据挖掘
机器学习
人工智能
模式识别(心理学)
生物
肽序列
基因
地理
操作系统
生物化学
大地测量学
作者
Gabriele Orlando,Daniele Raimondi,Taushif Khan,Tom Lenaerts,Wim Vranken
出处
期刊:Bioinformatics
[Oxford University Press]
日期:2017-06-28
卷期号:33 (24): 3902-3908
被引量:8
标识
DOI:10.1093/bioinformatics/btx391
摘要
Abstract Motivation Methods able to provide reliable protein alignments are crucial for many bioinformatics applications. In the last years many different algorithms have been developed and various kinds of information, from sequence conservation to secondary structure, have been used to improve the alignment performances. This is especially relevant for proteins with highly divergent sequences. However, recent works suggest that different features may have different importance in diverse protein classes and it would be an advantage to have more customizable approaches, capable to deal with different alignment definitions. Results Here we present Rigapollo, a highly flexible pairwise alignment method based on a pairwise HMM-SVM that can use any type of information to build alignments. Rigapollo lets the user decide the optimal features to align their protein class of interest. It outperforms current state of the art methods on two well-known benchmark datasets when aligning highly divergent sequences. Availability and implementation A Python implementation of the algorithm is available at http://ibsquare.be/rigapollo. Supplementary information Supplementary data are available at Bioinformatics online.
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