首页> 外文期刊>Nucleic Acids Research >Osprey: a comprehensive tool employing novel methods for the design of oligonucleotides for DNA sequencing and microarrays - art. no. e133
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Osprey: a comprehensive tool employing novel methods for the design of oligonucleotides for DNA sequencing and microarrays - art. no. e133

机译:Osprey:使用新颖方法的综合工具,用于设计DNA测序和微阵列的寡核苷酸-art。没有。 e133

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摘要

We have developed a software package called Osprey for the calculation of optimal oligonucleotides for DNA sequencing and the creation of microarrays based on either PCR-products or directly spotted oligomers. It incorporates a novel use of position-specific scoring matrices, for the sensitive and specific identification of secondary binding sites anywhere in the target sequence. Using accelerated hardware is faster and more efficient than the traditional pairwise alignments used in most oligo-design software. Osprey consists of a module for target site selection based on user input, novel utilities for dealing with problematic sequences such as repeats, and a common code base for the identification of optimal oligonucleotides from the target list. Overall, these improvements provide a program that, without major increases in run time, reflects current DNA thermodynamics models, improves specificity and reduces the user's data preprocessing and parameterization requirements. Using a TimeLogic(TM) hardware accelerator, we report up to 50-fold reduction in search time versus a linear search strategy. Target sites may be derived from computer analysis of DNA sequence assemblies in the case of sequencing efforts, or genome or EST analysis in the case of microarray development in both prokaryotes and eukaryotes.
机译:我们已经开发了一种名为Osprey的软件包,用于计算用于DNA测序的最佳寡核苷酸,并基于PCR产物或直接点样的寡聚物创建微阵列。它结合了位置特异性计分矩阵的新颖用途,用于灵敏且特异性地鉴定靶序列中任何位置的次级结合位点。与大多数oligo设计软件中使用的传统成对对齐方式相比,使用加速的硬件更快,更高效。 Osprey包括一个用于根据用户输入选择目标位点的模块,用于处理有问题的序列(例如重复序列)的新颖实用程序以及用于从目标列表中识别最佳寡核苷酸的通用代码库。总体而言,这些改进提供了一个程序,该程序无需大幅增加运行时间即可反映当前的DNA热力学模型,提高特异性并减少用户的数据预处理和参数化要求。与线性搜索策略相比,使用TimeLogic™硬件加速器,我们报告的搜索时间最多可减少50倍。在测序工作中,靶位点可从DNA序列装配体的计算机分析中得出,在原核生物和真核生物中,从微阵列发育的情况下,可从基因组或EST分析中得到。

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