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3A computational method for resequencing long DNA targets by universal oligonucleotide arrays

机译:3A通过通用寡核苷酸阵列对长DNA靶标进行重测序的计算方法

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Universal arrays contain all possible oligonucleotides of a certain length, typically 6-10 bases. They can determine in a single experiment all substrings of that length that occur along a target sequence. That information, also called the spectrum of the sequence, is not sufficient to uniquely reconstruct a sequence longer than a few hundred bases. We have devised a polynomial algorithm that reconstructs the sequence, given the spectrum and an additional reference sequence, homologous to the target sequence. Such a reference is available, for example, in the identification of single-nucleotide polymorphisms. The algorithm can handle errors in the spectrum as well as substitutions, insertions, and deletions in the target sequence. We present extensive simulation results, which show that the algorithm correctly reconstructs target sequences of >2,000 nucleotides from error-prone 8-mer spectra when realistic levels of single-nucleotide polymorphisms are present.
机译:通用阵列包含一定长度的所有可能的寡核苷酸,通常为6-10个碱基。他们可以在单个实验中确定沿着目标序列出现的该长度的所有子串。该信息(也称为序列的光谱)不足以唯一地重建长于几百个碱基的序列。我们设计了一种多项式算法,该算法可重构序列,并给出频谱和与目标序列同源的其他参考序列。这样的参考可用于例如单核苷酸多态性的鉴定。该算法可以处理光谱中的错误以及目标序列中的替换,插入和删除。我们提供了广泛的仿真结果,表明当存在现实水平的单核苷酸多态性时,该算法可从易于出错的8-mer光谱正确重建> 2,000个核苷酸的靶序列。

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