GapMis: a tool for pairwise sequence alignment with a single gap.

Tomás Flouri, Kimon Frousios, Costas S Iliopoulos, Kunsoo Park, Solon P Pissis, German Tischler
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引用次数: 10

Abstract

Motivation: Pairwise sequence alignment has received a new motivation due to the advent of recent patents in next-generation sequencing technologies, particularly so for the application of re-sequencing---the assembly of a genome directed by a reference sequence. After the fast alignment between a factor of the reference sequence and a high-quality fragment of a short read by a short-read alignment programme, an important problem is to find the alignment between a relatively short succeeding factor of the reference sequence and the remaining low-quality part of the read allowing a number of mismatches and the insertion of a single gap in the alignment.

Results: We present GapMis, a tool for pairwise sequence alignment with a single gap. It is based on a simple algorithm, which computes a different version of the traditional dynamic programming matrix. The presented experimental results demonstrate that GapMis is more suitable and efficient than most popular tools for this task.

GapMis:一个工具,两两序列比对与一个单一的差距。
动机:由于新一代测序技术专利的出现,成对序列比对获得了新的动机,特别是对于重测序的应用-由参考序列指导的基因组组装。在利用短读比对程序将参考序列的一个因子与短读片段的高质量片段快速比对之后,一个重要的问题是如何找到参考序列的一个相对较短的后续因子与剩余的低质量片段之间的比对,这些片段允许许多不匹配和在比对中插入单个间隙。结果:我们提出了GapMis,一种具有单个间隙的成对序列比对工具。它基于一种简单的算法,该算法计算传统动态规划矩阵的不同版本。实验结果表明,GapMis比大多数流行的工具更适合和有效地完成该任务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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