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Imputing missing values for genetic interaction data

机译:归咎于遗传交互数据的缺失值

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Background: Epistatic Miniarray Profiles (EMAP) enable the research of genetic interaction as an important method to construct large-scale genetic interaction networks. However, a high proportion of missing values frequently poses problems in EMAP data analysis since such missing values hinder downstream analysis. While some imputation approaches have been available to EMAP data, we adopted an improved SVD modeling procedure to impute the missing values in EMAP data which has resulted in a higher accuracy rate compared with existing methods. Results: The improved SVD imputation method adopts an effective soft-threshold to the SVD approach which has been shown to be the best model to impute genetic interaction data when compared with a number of advanced imputation methods. Imputation methods also improve the clustering results of EMAP datasets. Thus, after applying our imputation method on the EMAP dataset, more meaningful modules, known pathways and protein complexes could be detected. Conclusion: While the phenomenon of missing data unavoidably complicates EMAP data, our results showed that we could complete the original dataset by the Soft-SVD approach to accurately recover genetic interactions.
机译:背景:外观密闭剖面(EMAP)能够研究遗传相互作用作为构建大规模遗传互动网络的重要方法。然而,由于这种缺失的值阻碍下游分析,高比例缺失值频繁地造成了eMAP数据分析中的问题。虽然有些归纳方法已经用于映射数据,但我们采用了一种改进的SVD建模程序,以赋予EMAP数据中缺失值,这与现有方法相比具有更高的精度率。结果:改进的SVD归载方法采用有效的软阈值,对SVD方法被证明是与许多先进撤销方法相比施加遗传交互数据的最佳模型。估算方法还改善了EMAP数据集的聚类结果。因此,在在映射数据上施用普发上的方法之后,可以检测到更有意义的模块,已知的途径和蛋白质复合物。结论:虽然缺失数据的现象不可避免地使eMAP数据复杂化,但我们的结果表明我们可以通过软SVD方法完成原始数据集来准确地回收遗传交互。

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