A Low-Rank Representation Method Regularized by Dual-Hypergraph Laplacian for Selecting Differentially Expressed Genes

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY Human Heredity Pub Date : 2019-08-29 DOI:10.1159/000501482
Xiu-Xiu Xu, Lingyun Dai, Xiangzhen Kong, Jin-Xing Liu
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引用次数: 3

Abstract

Differentially expressed genes selection becomes a hotspot and difficulty in recent molecular biology. Low-rank representation (LRR) uniting graph Laplacian regularization has gained good achievement in the above field. However, the co-expression information of data cannot be captured well by graph regularization. Therefore, a novel low-rank representation method regularized by dual-hypergraph Laplacian is proposed to reveal the intrinsic geometrical structures hidden in the samples and genes direction simultaneously, which is called dual-hypergraph Laplacian regularized LRR (DHLRR). Finally, a low-rank matrix and a sparse perturbation matrix can be recovered from genomic data by DHLRR. Based on the sparsity of differentially expressed genes, the sparse disturbance matrix can be applied to extracting differentially expressed genes. In our experiments, two gene analysis tools are used to discuss the experimental results. The results on two real genomic data and an integrated dataset prove that DHLRR is efficient and effective in finding differentially expressed genes.
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用双超图拉普拉斯正则化的低秩表示方法选择差异表达基因
差异表达基因选择是近年来分子生物学研究的热点和难点。低秩表示(LRR)联合图拉普拉斯正则化在上述领域取得了良好的成果。然而,通过图正则化不能很好地捕捉数据的共表达信息。因此,提出了一种利用对偶超图拉普拉斯正则化的低秩表示方法,即对偶超图-拉普拉斯正则化LRR(DHLRR),以同时揭示隐藏在样本和基因方向上的内在几何结构。最后,DHLRR可以从基因组数据中恢复低秩矩阵和稀疏扰动矩阵。基于差异表达基因的稀疏性,稀疏干扰矩阵可以用于提取差异表达基因。在我们的实验中,使用了两种基因分析工具来讨论实验结果。两个真实基因组数据和一个综合数据集的结果证明DHLRR在寻找差异表达基因方面是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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