发现远端ncRNA同源物的定制策略。

Briefings in functional genomics & proteomics Pub Date : 2009-11-01 Epub Date: 2009-09-24 DOI:10.1093/bfgp/elp035
Axel Mosig, Liang Zhu, Peter F Stadler
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引用次数: 26

摘要

很大一部分非编码rna是短的和/或在序列上保守性差。此外,大多数较长的例子由保守的结构基元组成,而不是一个连贯的全局保守的二级结构。结果,同源搜索这个概念上简单的问题变成了一个复杂且技术要求很高的任务。尽管Rfam等数据库尽了最大努力,但由于许多RNA家族(特别是原核RNA家族)信息的稀疏性,情况进一步复杂化。在这篇文章中,我们回顾了最近为ncRNA应用定制基于序列的搜索工具的努力。特别是,半全局对齐和碎片模式搜索方法的发展带来了重大的实际进展。目前该领域的发展主要集中在碎片序列模式搜索与二级结构模式搜索算法的集成上。我们在此特别关注那些能够在“模糊地带”取得成功的策略,即从爆炸到地狱到开始失败的一般方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Customized strategies for discovering distant ncRNA homologs.

A large fraction of non-coding RNAs is short and/or poorly conserved in sequence. Most of the longer examples, furthermore, consist of a collection of conserved structural motifs rather than a coherent globally conserved secondary structure. As a consequence, the conceptually simple problem of homology search becomes a complex and technically demanding task. Despite the best efforts of databases such as Rfam, the situation is complicated further by the sparsity of information in many--in particular prokaryotic--RNA families. In this contribution, we review recent efforts to customize sequence-based search tools for ncRNA applications. In particular, semi-global alignments and the development of methods for fragmented pattern search have brought significant practical advances. Current developments in this area focus on the integration of fragmented sequence pattern search with search algorithms for secondary structure patterns. We focus here, in particular, on strategies that can be successful in the 'twilight zone' where generic approaches from blast to infernal to start to fail.

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