Degenerate primer design via clustering.

Xintao Wei, David N Kuhn, Giri Narasimhan
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引用次数: 0

Abstract

This paper describes a new strategy for designing degenerate primers for a given multiple alignment of amino acid sequences. Degenerate primers are useful for amplifying homologous genes. However, when a large collection of sequences is considered, no consensus region may exist in the multiple alignment, making it impossible to design a single pair of primers for the collection. In such cases, manual methods are used to find smaller groups from the input collection so that primers can be designed for individual groups. Our strategy proposes an automatic grouping of the input sequences by using clustering techniques. Conserved regions are then detected for each individual group. Conserved regions are scored using a BlockSimilarity score, a novel alignment scoring scheme that is appropriate for this application. Degenerate primers are then designed by reverse translating the conserved amino acid sequences to the corresponding nucleotide sequences. Our program, DePiCt, was written in BioPerl and was tested on the Toll-Interleukin Receptor (TIR)and the non-TIR family of plant resistance genes. Existing programs for degenerate primer design were unable to find primers for these data sets.

通过聚类简化引物设计。
本文描述了一种设计退化引物的新策略,用于给定的氨基酸序列的多重比对。简并引物用于扩增同源基因。然而,当考虑一个大的序列集合时,多重比对中可能不存在一致区域,因此不可能为该集合设计一对引物。在这种情况下,使用手动方法从输入集合中找到较小的组,以便为单个组设计引物。我们提出了一种使用聚类技术对输入序列进行自动分组的策略。然后为每个单独的组检测保守区域。使用BlockSimilarity评分对保守区域进行评分,这是一种适用于此应用的新颖对齐评分方案。然后通过将保守的氨基酸序列反向翻译成相应的核苷酸序列来设计简并引物。我们的程序描述是用BioPerl编写的,并在Toll-Interleukin Receptor (TIR)和非TIR家族的植物抗性基因上进行了测试。现有的退化引物设计程序无法为这些数据集找到引物。
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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