Identifying subspace gene clusters from microarray data using low-rank representation.

Identifying subspace gene clusters from the gene expression data is useful for discovering novel functional gene interactions. In this paper, we propose to use low-rank representation (LRR) to identify the subspace gene clusters from microarray data. LRR seeks the lowest-rank representation among al...

Full description

Bibliographic Details
Main Authors: Yan Cui, Chun-Hou Zheng, Jian Yang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23527177/?tool=EBI
id doaj-d8dc02d66f4a411f8de1c2282c962c8b
record_format Article
spelling doaj-d8dc02d66f4a411f8de1c2282c962c8b2021-03-03T20:24:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5937710.1371/journal.pone.0059377Identifying subspace gene clusters from microarray data using low-rank representation.Yan CuiChun-Hou ZhengJian YangIdentifying subspace gene clusters from the gene expression data is useful for discovering novel functional gene interactions. In this paper, we propose to use low-rank representation (LRR) to identify the subspace gene clusters from microarray data. LRR seeks the lowest-rank representation among all the candidates that can represent the genes as linear combinations of the bases in the dataset. The clusters can be extracted based on the block diagonal representation matrix obtained using LRR, and they can well capture the intrinsic patterns of genes with similar functions. Meanwhile, the parameter of LRR can balance the effect of noise so that the method is capable of extracting useful information from the data with high level of background noise. Compared with traditional methods, our approach can identify genes with similar functions yet without similar expression profiles. Also, it could assign one gene into different clusters. Moreover, our method is robust to the noise and can identify more biologically relevant gene clusters. When applied to three public datasets, the results show that the LRR based method is superior to existing methods for identifying subspace gene clusters.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23527177/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Yan Cui
Chun-Hou Zheng
Jian Yang
spellingShingle Yan Cui
Chun-Hou Zheng
Jian Yang
Identifying subspace gene clusters from microarray data using low-rank representation.
PLoS ONE
author_facet Yan Cui
Chun-Hou Zheng
Jian Yang
author_sort Yan Cui
title Identifying subspace gene clusters from microarray data using low-rank representation.
title_short Identifying subspace gene clusters from microarray data using low-rank representation.
title_full Identifying subspace gene clusters from microarray data using low-rank representation.
title_fullStr Identifying subspace gene clusters from microarray data using low-rank representation.
title_full_unstemmed Identifying subspace gene clusters from microarray data using low-rank representation.
title_sort identifying subspace gene clusters from microarray data using low-rank representation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Identifying subspace gene clusters from the gene expression data is useful for discovering novel functional gene interactions. In this paper, we propose to use low-rank representation (LRR) to identify the subspace gene clusters from microarray data. LRR seeks the lowest-rank representation among all the candidates that can represent the genes as linear combinations of the bases in the dataset. The clusters can be extracted based on the block diagonal representation matrix obtained using LRR, and they can well capture the intrinsic patterns of genes with similar functions. Meanwhile, the parameter of LRR can balance the effect of noise so that the method is capable of extracting useful information from the data with high level of background noise. Compared with traditional methods, our approach can identify genes with similar functions yet without similar expression profiles. Also, it could assign one gene into different clusters. Moreover, our method is robust to the noise and can identify more biologically relevant gene clusters. When applied to three public datasets, the results show that the LRR based method is superior to existing methods for identifying subspace gene clusters.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23527177/?tool=EBI
work_keys_str_mv AT yancui identifyingsubspacegeneclustersfrommicroarraydatausinglowrankrepresentation
AT chunhouzheng identifyingsubspacegeneclustersfrommicroarraydatausinglowrankrepresentation
AT jianyang identifyingsubspacegeneclustersfrommicroarraydatausinglowrankrepresentation
_version_ 1714822680046206976