Improved prediction of transcription binding sites from chromatin modification data

Kengo Sato, Thomas Whitington, T. Bailey, P. Horton
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Abstract

In this paper we apply machine learning to the task of predicting transcription factor binding sites by combining information on multiple forms of chromatin modification with the binding strength DNA site predicted by a position weight matrix. We additionally explore the effect of incorporating auxiliary features such as the distance of the site to the nearest gene's transcription start site and the degree to which the site is conserved among related species. We approach the task as a classification problem, and show that both Na¨ıve Bayes and Random Forests can provide substantial increases in the accuracy of predicted binding sites. Our results extend previous work which simply filtered candidate sites based on H3K4Me3 chromatin modification scores. In addition we apply feature selection to explore which forms of chromatin modification and which auxiliary features have predictive value for which transcription factors.
利用染色质修饰数据改进转录结合位点的预测
在本文中,我们将机器学习应用于预测转录因子结合位点的任务,通过结合多种形式的染色质修饰信息和由位置权重矩阵预测的结合强度DNA位点。我们还探讨了纳入辅助特征的影响,例如该位点与最近基因转录起始位点的距离以及该位点在相关物种中的保守程度。我们将该任务视为分类问题,并表明Na¨ıve贝叶斯和随机森林都可以大幅提高预测结合位点的准确性。我们的结果扩展了先前的工作,即简单地根据H3K4Me3染色质修饰分数过滤候选位点。此外,我们应用特征选择来探索哪些形式的染色质修饰和哪些辅助特征对哪些转录因子具有预测价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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