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SPARSE: quadratic time simultaneous alignment and folding of RNAs without sequence-based heuristics

机译:SPARSE:二次时间同时对齐和折叠RNA,无需基于序列的启发式

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Motivation: RNA-Seq experiments have revealed a multitude of novel ncRNAs. The gold standard for their analysis based on simultaneous alignment and folding suffers from extreme time complexity of O(n(6)). Subsequently, numerous faster 'Sankoff-style' approaches have been suggested. Commonly, the performance of such methods relies on sequence-based heuristics that restrict the search space to optimal or near-optimal sequence alignments; however, the accuracy of sequence-based methods breaks down for RNAs with sequence identities below 60%. Alignment approaches like LocARNA that do not require sequence-based heuristics, have been limited to high complexity (>= quartic time).
机译:动机:RNA-Seq实验揭示了许多新颖的ncRNA。用于基于同时对齐和折叠的分析的金标准遭受O(n(6))的极端时间复杂性的困扰。随后,提出了许多更快的“桑科夫式”方法。通常,此类方法的性能依赖于基于序列的启发式算法,该算法将搜索空间限制为最佳或接近最佳的序列比对。但是,基于序列的方法的准确性会破坏序列同一性低于60%的RNA。诸如LocARNA之类的不需要基于序列的试探法的比对方法仅限于高复杂度(> =四次时间)。

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