Liu Derong, Xiong Xiaoxu, DasGupta Bhaskar, Zhang Huaguang
IEEE Trans Neural Netw. 2006 Jul;17(4):919-928. doi: 10.1109/TNN.2006.875987.
In this paper, we study the problem of motif discoveries in unaligned DNA and protein sequences. The problem of motif identification in DNA and protein sequences has been studied for many years in the literature. Major hurdles at this point include computational complexity and reliability of the search algorithms. We propose a self-organizing neural network structure for solving the problem of motif identification in DNA and protein sequences. Our network contains several layers, with each layer performing classifications at different levels. The top layer divides the input space into a small number of regions and the bottom layer classifies all input patterns into motifs and nonmotif patterns. Depending on the number of input patterns to be classified, several layers between the top layer and the bottom layer are needed to perform intermediate classifications. We maintain a low computational complexity through the use of the layered structure so that each pattern's classification is performed with respect to a small subspace of the whole input space. Our self-organizing neural network will grow as needed (e.g., when more motif patterns are classified). It will give the same amount of attention to each input pattern and will not omit any potential motif patterns. Finally, simulation results show that our algorithm outperforms existing algorithms in certain aspects. In particular, simulation results show that our algorithm can identify motifs with more mutations than existing algorithms. Our algorithm works well for long DNA sequences as well.
在本文中,我们研究了未比对的DNA和蛋白质序列中的基序发现问题。DNA和蛋白质序列中的基序识别问题在文献中已被研究多年。目前的主要障碍包括计算复杂性和搜索算法的可靠性。我们提出了一种自组织神经网络结构来解决DNA和蛋白质序列中的基序识别问题。我们的网络包含若干层,每层在不同层次上进行分类。顶层将输入空间划分为少量区域,底层将所有输入模式分类为基序模式和非基序模式。根据要分类的输入模式数量,需要在顶层和底层之间设置若干层来进行中间分类。通过使用分层结构,我们保持了较低的计算复杂性,以便针对整个输入空间的一个小子空间对每个模式进行分类。我们的自组织神经网络将根据需要进行扩展(例如,当分类更多的基序模式时)。它将对每个输入模式给予同等程度的关注,不会遗漏任何潜在的基序模式。最后,仿真结果表明,我们的算法在某些方面优于现有算法。特别是,仿真结果表明,我们的算法能够识别比现有算法更多具有突变的基序。我们的算法对于长DNA序列也能很好地发挥作用。