lncDIFF: a novel quasi-likelihood method for differential expression analysis of non-coding RNA

Abstract Background Long non-coding RNA (lncRNA) expression data have been increasingly used in finding diagnostic and prognostic biomarkers in cancer studies. Existing differential analysis tools for RNA sequencing do not effectively accommodate low abundant genes, as commonly observed in lncRNAs....

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Main Authors: Qian Li, Xiaoqing Yu, Ritu Chaudhary, Robbert J. C. Slebos, Christine H. Chung, Xuefeng Wang
Format: Article
Language:English
Published: BMC 2019-07-01
Series:BMC Genomics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12864-019-5926-4
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spelling doaj-c629c2bdb9d74427a0be5445d7dc0ad82020-11-25T03:07:24ZengBMCBMC Genomics1471-21642019-07-0120111310.1186/s12864-019-5926-4lncDIFF: a novel quasi-likelihood method for differential expression analysis of non-coding RNAQian Li0Xiaoqing Yu1Ritu Chaudhary2Robbert J. C. Slebos3Christine H. Chung4Xuefeng Wang5Health Informatics Institute, University of South FloridaDepartment of Biostatistics and Bioinformatics, Moffitt Cancer CenterDepartment of Head and Neck-Endocrine Oncology, Moffitt Cancer CenterDepartment of Head and Neck-Endocrine Oncology, Moffitt Cancer CenterDepartment of Head and Neck-Endocrine Oncology, Moffitt Cancer CenterDepartment of Biostatistics and Bioinformatics, Moffitt Cancer CenterAbstract Background Long non-coding RNA (lncRNA) expression data have been increasingly used in finding diagnostic and prognostic biomarkers in cancer studies. Existing differential analysis tools for RNA sequencing do not effectively accommodate low abundant genes, as commonly observed in lncRNAs. Results We investigated the statistical distribution of normalized counts for low expression genes in lncRNAs and mRNAs, and proposed a new tool lncDIFF based on the underlying distribution pattern to detect differentially expressed (DE) lncRNAs. lncDIFF adopts the generalized linear model with zero-inflated Exponential quasi-likelihood to estimate group effect on normalized counts, and employs the likelihood ratio test to detect differential expressed genes. The proposed method and tool are applicable to data processed with standard RNA-Seq preprocessing and normalization pipelines. Simulation results showed that lncDIFF was able to detect DE genes with more power and lower false discovery rate regardless of the data pattern, compared to DESeq2, edgeR, limma, zinbwave, DEsingle, and ShrinkBayes. In the analysis of a head and neck squamous cell carcinomas data, lncDIFF also appeared to have higher sensitivity in identifying novel lncRNA genes with relatively large fold change and prognostic value. Conclusions lncDIFF is a powerful differential analysis tool for low abundance non-coding RNA expression data. This method is compatible with various existing RNA-Seq quantification and normalization tools. lncDIFF is implemented in an R package available at https://github.com/qianli10000/lncDIFF.http://link.springer.com/article/10.1186/s12864-019-5926-4lncRNADifferential analysisQuasi-likelihoodHead and neck squamous cell carcinomas
collection DOAJ
language English
format Article
sources DOAJ
author Qian Li
Xiaoqing Yu
Ritu Chaudhary
Robbert J. C. Slebos
Christine H. Chung
Xuefeng Wang
spellingShingle Qian Li
Xiaoqing Yu
Ritu Chaudhary
Robbert J. C. Slebos
Christine H. Chung
Xuefeng Wang
lncDIFF: a novel quasi-likelihood method for differential expression analysis of non-coding RNA
BMC Genomics
lncRNA
Differential analysis
Quasi-likelihood
Head and neck squamous cell carcinomas
author_facet Qian Li
Xiaoqing Yu
Ritu Chaudhary
Robbert J. C. Slebos
Christine H. Chung
Xuefeng Wang
author_sort Qian Li
title lncDIFF: a novel quasi-likelihood method for differential expression analysis of non-coding RNA
title_short lncDIFF: a novel quasi-likelihood method for differential expression analysis of non-coding RNA
title_full lncDIFF: a novel quasi-likelihood method for differential expression analysis of non-coding RNA
title_fullStr lncDIFF: a novel quasi-likelihood method for differential expression analysis of non-coding RNA
title_full_unstemmed lncDIFF: a novel quasi-likelihood method for differential expression analysis of non-coding RNA
title_sort lncdiff: a novel quasi-likelihood method for differential expression analysis of non-coding rna
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2019-07-01
description Abstract Background Long non-coding RNA (lncRNA) expression data have been increasingly used in finding diagnostic and prognostic biomarkers in cancer studies. Existing differential analysis tools for RNA sequencing do not effectively accommodate low abundant genes, as commonly observed in lncRNAs. Results We investigated the statistical distribution of normalized counts for low expression genes in lncRNAs and mRNAs, and proposed a new tool lncDIFF based on the underlying distribution pattern to detect differentially expressed (DE) lncRNAs. lncDIFF adopts the generalized linear model with zero-inflated Exponential quasi-likelihood to estimate group effect on normalized counts, and employs the likelihood ratio test to detect differential expressed genes. The proposed method and tool are applicable to data processed with standard RNA-Seq preprocessing and normalization pipelines. Simulation results showed that lncDIFF was able to detect DE genes with more power and lower false discovery rate regardless of the data pattern, compared to DESeq2, edgeR, limma, zinbwave, DEsingle, and ShrinkBayes. In the analysis of a head and neck squamous cell carcinomas data, lncDIFF also appeared to have higher sensitivity in identifying novel lncRNA genes with relatively large fold change and prognostic value. Conclusions lncDIFF is a powerful differential analysis tool for low abundance non-coding RNA expression data. This method is compatible with various existing RNA-Seq quantification and normalization tools. lncDIFF is implemented in an R package available at https://github.com/qianli10000/lncDIFF.
topic lncRNA
Differential analysis
Quasi-likelihood
Head and neck squamous cell carcinomas
url http://link.springer.com/article/10.1186/s12864-019-5926-4
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