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A SUBSPACE METHOD FOR THE DETECTION OF TRANSCRIPTION FACTOR BINDING SITES

机译:检测转录因子结合位点的子空间方法

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Transcription Factor binding sites are short and degenerate sequences, located mostly at the promoter of the gene, where some proteins bind in order to regulate transcription. Locating these sequences is an important issue, and many experimental and computational methods have been developed. Algorithms to search binding sites are usually based on Position Specific Scoring Matrices (PSSM), where each position is treated independently. Mapping symbolical DNA to numerical sequences, a detector has been built with a Principal Component Analysis of the numerical sequences, taking into account covariances between positions. When a treatment of missing values is incorporated the Q-residuals detector, based on PCA, performs better than a PSSM algorithm. The performance on the detector depends on the estimation of missing values and the percentage of missing values considered in the model.
机译:转录因子结合位点是短期和简并序列,主要位于基因的启动子,其中一些蛋白质结合以调节转录。定位这些序列是一个重要问题,并且已经开发了许多实验和计算方法。搜索绑定站点的算法通常基于位置特定的评分矩阵(PSSM),其中每个位置被独立处理。将符号DNA映射到数值序列,通过数值分析构建了探测器,以考虑到位置之间的协方差。当缺失值的处理结合到基于PCA的Q-Residals检测器时,比PSSM算法更好地执行。探测器上的性能取决于缺失值的估计和模型中考虑的缺失值的百分比。

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