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A Randomized Algorithm for Aligning DNA Sequences to Reference Genomes

机译:一种随机算法,用于将DNA序列对准引用基因组

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The alignment of reads generated by next- generation sequencers is an important problem in many biomedical applications. Although many methods have been proposed, we introduce a new randomized algorithm with the distinction of having high performance across a wide range of read lengths and base error rates. We utilize two FM indices to facilitate efficient bidirectional searching. Randomization allows us to estimate effectively key parameters, which ultimately account for the consistency in performance of the method. Our method by and large outperformed some of the recent and popular methods over a wide range of read lengths and base error rates.
机译:由下一代定序器生成的读取的对齐是许多生物医学应用中的重要问题。虽然已经提出了许多方法,但我们介绍了一种新的随机化算法,其区别在各种读取长度和基本误差速率方面具有高性能。我们利用两个FM指数来促进高效的双向搜索。随机化允许我们估计有效的关键参数,最终占该方法性能的一致性。我们的方法和大量优于近期读取长度和基本误差率的最近和流行的一些方法。

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