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PALMA: mRNA to genome alignments using large margin algorithms

机译:PALMA:使用大边距算法对mRNA与基因组进行比对

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Motivation: Despite many years of research on how to properly align sequences in the presence of sequencing errors, alternative splicing and micro-exons, the correct alignment of mRNA sequences to genomic DNA is still a challenging task. Results: We present a novel approach based on large margin learning that combines accurate splice site predictions with common sequence alignment techniques. By solving a convex optimization problem, our algorithm-called PALMA-tunes the parameters of the model such that true alignments score higher than other alignments. We study the accuracy of alignments of mRNAs containing artificially generated micro-exons to genomic DNA. In a carefully designed experiment, we show that our algorithm accurately identifies the intron boundaries as well as boundaries of the optimal local alignment. It outperforms all other methods: for 5702 artificially shortened EST sequences from Caenorhabditis elegans and human, it correctly identifies the intron boundaries in all except two cases. The best other method is a recently proposed method called exalin which misaligns 37 of the sequences. Our method also demonstrates robustness to mutations, insertions and deletions, retaining accuracy even at high noise levels.
机译:动机:尽管在如何进行序列错误,选择性剪接和微外显子存在下如何正确比对序列方面进行了多年的研究,但将mRNA序列与基因组DNA正确比对仍然是一项艰巨的任务。结果:我们提出了一种基于大幅度学习的新颖方法,该方法将准确的剪接位点预测与常见的序列比对技术相结合。通过解决凸优化问题,我们的算法称为PALMA调整模型的参数,以使真实比对的得分高于其他比对。我们研究了包含人工生成的微外显子与基因组DNA的mRNA的比对准确性。在精心设计的实验中,我们证明了我们的算法可准确识别内含子边界以及最佳局部比对的边界。它优于其他所有方法:对于线虫和人的5702人为缩短的EST序列,它可以正确识别除两种情况以外的所有内含子边界。最好的另一种方法是最近提出的一种名为exalin的方法,该方法可使37个序列错位。我们的方法还证明了对突变,插入和缺失的鲁棒性,即使在高噪声水平下也能保持准确性。

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