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Approximation Algorithms for Minimum PCR Primer Set Selection with Amplification Length and Uniqueness Constraints

机译:最小pCR引物组选择的近似算法   扩增长度和唯一性约束

摘要

A critical problem in the emerging high-throughput genotyping protocols is tominimize the number of polymerase chain reaction (PCR) primers required toamplify the single nucleotide polymorphism loci of interest. In this paper westudy PCR primer set selection with amplification length and uniquenessconstraints from both theoretical and practical perspectives. We give a greedyalgorithm that achieves a logarithmic approximation factor for the problem ofminimizing the number of primers subject to a given upperbound on the length ofPCR amplification products. We also give, using randomized rounding, the firstnon-trivial approximation algorithm for a version of the problem that requiresunique amplification of each amplification target. Empirical results onrandomly generated testcases as well as testcases extracted from the from theNational Center for Biotechnology Information's genomic databases show that ouralgorithms are highly scalable and produce better results compared to previousheuristics.
机译:新兴的高通量基因分型方案中的一个关键问题是最小化扩增目标单核苷酸多态性基因座所需的聚合酶链反应(PCR)引物的数量。本文从理论和实践的角度对具有扩增长度和唯一性约束的westudy PCR引物进行选择。我们给出了一个贪婪算法,该算法可实现对数逼近因子,以解决在PCR扩增产物的长度上受给定上限限制的引物数量最小的问题。我们还使用随机舍入为需要每个扩增靶点唯一扩增的问题版本提供了第一个非平凡逼近算法。随机生成的测试用例以及从国家生物技术信息中心的基因组数据库中提取的测试用例的经验结果表明,与以前的启发式算法相比,我们的算法具有很高的可扩展性并产生更好的结果。

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