A rectified factor network based biclustering method for detecting cancer-related coding genes and miRNAs, and their interactions

被引:3
|
作者
Su, Lingtao [1 ,2 ,3 ]
Liu, Guixia [1 ]
Wang, Juexin [2 ,3 ]
Xu, Dong [2 ,3 ]
机构
[1] Jilin Univ, Dept Comp Sci & Technol, Changchun 130012, Jilin, Peoples R China
[2] Univ Missouri, Dept Elect Engn & Comp Sci, Columbia, MO 65211 USA
[3] Univ Missouri, Christopher S Bond Life Sci Ctr, Columbia, MO 65211 USA
基金
美国国家卫生研究院;
关键词
Rectified factor networks; Biclustering; Biomarker; miRNA; Gene-miRNA interaction; Breast cancer; BREAST-CANCER; MESSENGER-RNA; R-PACKAGE; MICRORNA; PRIORITIZATION; EXPRESSION; IDENTIFICATION; LUNG; BIOMARKERS; DATABASE;
D O I
10.1016/j.ymeth.2019.05.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Detecting cancer-related genes and their interactions is a crucial task in cancer research. For this purpose, we proposed an efficient method, to detect coding genes, microRNAs (miRNAs), and their interactions related to a particular cancer or a cancer subtype using their expression data from the same set of samples. Firstly, biclusters specific to a particular type of cancer are detected based on rectified factor networks and ranked according to their associations with general cancers. Secondly, coding genes and miRNAs in each bicluster are prioritized by considering their differential expression and differential correlation values, protein protein interaction data, and potential cancer markers. Finally, a rank fusion process is used to obtain the final comprehensive rank by combining multiple ranking results. We applied our proposed method on breast cancer datasets. Results show that our method outperforms other methods in detecting breast cancer-related coding genes and miRNAs. Furthermore, our method is very efficient in computing time, which can handle tens of thousands genes/miRNAs and hundreds of patients in hours on a desktop. This work may aid researchers in studying the genetic architecture of complex diseases, and improving the accuracy of diagnosis.
引用
收藏
页码:22 / 30
页数:9
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