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A New Weighted Imputed Neighborhood-Regularized Tri-Factorization One-Class Collaborative Filtering Algorithm: Application to Target Gene Prediction of Transcription Factors

机译:一种新的加权抵抗邻域正规化三重分解一类协同过滤算法:应用于靶向转录因子的基因预测

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摘要

Identifying target genes of transcription factors (TFs) is crucial to understand transcriptional regulation. However, our understanding of genome-wide TF targeting profile is limited due to the cost of large-scale experiments and intrinsic complexity of gene regulation. Thus, computational prediction methods are useful to predict unobserved TF-gene associations. Here, we develop a new Weighted Imputed Neighborhood-regularized Tri-Factorization one-class collaborative filtering algorithm, WINTF. It predicts unobserved target genes for TFs using known but noisy, incomplete, and biased TF-gene associations and protein-protein interaction networks. Our benchmark study shows that WINTF significantly outperforms its counterpart matrix factorization-based algorithms and tri-factorization methods that do not include weight, imputation, and neighbor-regularization, for TF-gene association prediction. When evaluated by independent datasets, accuracy is 37.8 percent on the top 495 predicted associations, an enrichment factor of 4.19 compared with random guess. Furthermore, many predicted novel associations are supported by literature evidence. Although we only use canonical TF-gene interaction data, WINTF can directly be applied to tissue-specific data when available. Thus, WINTF provides a potentially useful framework to integrate multiple omics data for further improvement of TF-gene prediction and applications to other sparse and noisy biological data. The benchmark dataset and source code are freely available at https://github.corn/XieResearchGroup/WINTF.
机译:鉴定转录因子(TFS)的靶基因对于了解转录调节至关重要。然而,由于大规模实验的成本和基因调节的内在复杂性,我们对基因组宽的TF靶向简档的理解受到限制。因此,计算预测方法可用于预测未观察到的TF基因关联。在这里,我们开发了一种新的加权抵抗邻域正规化的三重分解一类协作滤波算法WINTF。使用已知但嘈杂,不完整和偏置的TF-基因关联和蛋白质蛋白质相互作用网络预测用于TFS的未观察到的靶基因。我们的基准研究表明,Wintf显着优于其对应基于矩阵分子的算法和三分化方法,其不包括TF-基因关联预测的重量,归纳和邻正则化。当由独立数据集进行评估时,最高495个预测关联的准确度为37.8%,与随机猜测相比,富集因子为4.19。此外,许多预测的新型关联由文献证据支持。虽然我们只使用规范TF-Gene交互数据,但是在可用时,Wintf可以直接应用于特定于组织的数据。因此,WINTF提供了潜在有用的框架,以集成多个OMIC数据以进一步改进TF-基因预测和应用于其他稀疏和嘈杂的生物数据。基准数据集和源代码可在https://github.corn/xieresearchgroup/wintf上自由使用。

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