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Improving promoter prediction Improving promoter prediction for the NNPP2.2 algorithm: a case study using Escherichia coli DNA sequences

机译:改进启动子预测改进NNPP2.2算法的启动子预测:使用大肠杆菌DNA序列的案例研究

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摘要

Motivation: Although a great deal of research has been undertaken in the area of promoter prediction, prediction techniques are still not fully developed. Many algorithms tend to exhibit poor specificity, generating many false positives, or poor sensitivity. The neural network prediction program NNPP2.2 is one such example.Results: To improve the NNPP2.2 prediction technique, the distance between the transcription start site (TSS) associated with the promoter and the translation start site (TLS) of the subsequent gene coding region has been studied for Escherichia coli K12 bacteria. An empirical probability distribution that is consistent for all E.coli promoters has been established. This information is combined with the results from NNPP2.2 to create a new technique called TLS-NNPP, which improves the specificity of promoter prediction. The technique is shown to be effective using E.coli DNA sequences, however, it is applicable to any organism for which a set of promoters has been experimentally defined.
机译:动机:尽管在启动子预测领域进行了大量研究,但预测技术仍未完全开发。许多算法往往表现出较差的特异性,生成许多假阳性或较差的灵敏度。神经网络预测程序NNPP2.2就是这样的一个例子。结果:为了改进NNPP2.2预测技术,与启动子相关的转录起始位点(TSS)与后续基因的翻译起始位点(TLS)之间的距离已经研究了大肠杆菌K12细菌的编码区。建立了与所有大肠杆菌启动子一致的经验概率分布。该信息与NNPP2.2的结果相结合,创建了一种称为TLS-NNPP的新技术,该技术提高了启动子预测的特异性。该技术显示使用大肠杆菌DNA序列是有效的,但是,它适用于已通过实验确定了一组启动子的任何生物。

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