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A pHMM-ANN based discriminative approach to promoter identification in prokaryote genomic contexts

机译:基于pHMM-ANN的原核生物基因组环境下启动子识别的判别方法

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The computational approach for identifying promoters on increasingly large genomic sequences has led to many false positives. The biological significance of promoter identification lies in the ability to locate true promoters with and without prior sequence contextual knowledge. Prior approaches to promoter modelling have involved artificial neural networks (ANNs) or hidden Markov models (HMMs), each producing adequate results on small scale identification tasks, i.e. narrow upstream regions. In this work, we present an architecture to support prokaryote promoter identification on large scale genomic sequences, i.e. not limited to narrow upstream regions. The significant contribution involved the hybrid formed via aggregation of the profile HMM with the ANN, via Viterbi scoring optimizations. The benefit obtained using this architecture includes the modelling ability of the profile HMM with the ability of the ANN to associate elements composing the promoter. We present the high effectiveness of the hybrid approach in comparison to profile HMMs and ANNs when used separately. The contribution of Viterbi optimizations is also highlighted for supporting the hybrid architecture in which gains in sensitivity (+0.3), specificity (+0.65) and precision (+0.54) are achieved over existing approaches.
机译:在越来越大的基因组序列上鉴定启动子的计算方法导致了许多假阳性。启动子鉴定的生物学意义在于在有或没有先验序列背景知识的情况下定位真正的启动子的能力。启动子建模的先前方法涉及人工神经网络(ANN)或隐马尔可夫模型(HMM),每种方法都能在小规模识别任务(即狭窄的上游区域)上产生足够的结果。在这项工作中,我们提出了一种在大规模基因组序列上支持原核生物启动子鉴定的体系结构,即不限于狭窄的上游区域。重大贡献涉及通过将轮廓HMM与ANN聚合,通过维特比评分优化而形成的混合动力。使用此架构获得的好处包括配置文件HMM的建模能力和ANN关联组成启动子的元素的能力。与单独使用轮廓HMM和ANN相比,我们展示了混合方法的高效性。还强调了维特比优化的贡献,以支持混合体系结构,与现有方法相比,该体系结构在灵敏度(+0.3),特异性(+0.65)和精度(+0.54)方面获得了增长。

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