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TV-DCT: Method to Impute Gene Expression Data Using DCT Based Sparsity and Total Variation Denoising

机译:TV-DCT:使用基于DCT的稀疏度和总变异去噪来估算基因表达数据的方法

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摘要

Most of the bioinformatics tools used in the analysis of gene expression data require complete data matrices. Missing values in data can adversely influence the downstream analysis for diagnostics and treatment. Several methods to impute missing values in gene data have been developed. However, most of these work at high levels of observability. In this paper, we have proposed a novel 2-stage method, namely, TV-DCT for imputing incomplete gene expression matrices using Total Variation denoising and Discrete Cosine Transform Domain Sparsity (TV-DCT) that achieves smaller imputation errors, consistently, at all levels of observability. The proposed method has been compared with three state-of-the-art matrix completion methods on three different cancer datasets and is observed to perform better. The validation of imputed data has been demonstrated on the application of classification.
机译:用于基因表达数据分析的大多数生物信息学工具都需要完整的数据矩阵。数据中缺少的值可能会对诊断和治疗的下游分析产生不利影响。已经开发出几种估算基因数据中缺失值的方法。但是,其中大多数工作都是在较高的可观察性下进行的。在本文中,我们提出了一种新颖的两阶段方法,即使用总变异去噪和离散余弦变换域稀疏性(TV-DCT)来插补不完全基因表达矩阵的TV-DCT,该插补误差始终较小。可观察性水平。在三种不同的癌症数据集上,将所提出的方法与三种最新的矩阵完成方法进行了比较,并观察到其性能更好。归类数据的验证已在分类的应用中得到证明。

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