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Rapid large-scale oligonucleotide selection for microarrays

机译:快速大规模选择寡核苷酸用于微阵列

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We present the first algorithm that selects oligonucleotide probes (e.g. 25-mers) for microarray experiments on a large scale. For example, oligos for human genes can be found within 50 hours. This becomes possible by using the longest common substring as a specificity measure for candidate oligos. We present an algorithm based on a suffix array with additional information that is efficient both in terms of memory usage and running time to rank all candidate oligos according to their specificity. We also introduce the concept of master sequences to describe the sequences from which oligos are to be selected. Constraints such as oligo length, melting temperature, and self-complementarity are incorporated in the master sequence at a preprocessing stage and thus kept separate from the main selection problem. As a result, custom oligos can now be designed for any sequenced genome, just as the technology for on-site chip synthesis is becoming increasingly mature.
机译:我们提出了第一种选择用于大规模微阵列实验的寡核苷酸探针(例如25-mers)的算法。例如,可以在50小时内找到人类基因的寡核苷酸。通过使用最长的公共子串作为候选寡核苷酸的特异性度量,这成为可能。我们提出了一种基于后缀数组的算法,该算法具有附加信息,可根据内存使用率和运行时间高效地对所有候选寡核苷酸根据其特异性进行排名。我们还介绍了主序列的概念,以描述从中选择寡核苷酸的序列。诸如寡核苷酸长度,解链温度和自互补性之类的约束条件在预处理阶段并入主序列中,因此与主要选择问题保持分离。结果,就像用于现场芯片合成的技术日趋成熟一样,现在可以为任何测序的基因组设计定制的寡核苷酸。

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