An Integrated Approach for RNA-seq Data Normalization

被引:5
|
作者
Yang, Shengping [1 ,2 ]
Mercante, Donald E. [2 ]
Zhang, Kun [3 ]
Fang, Zhide [2 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Sch Med, Dept Pathol, Lubbock, TX 79430 USA
[2] LSU Hlth Sci Ctr, Sch Publ Hlth, Biostat Program, New Orleans, LA 70112 USA
[3] Xavier Univ Louisiana, Dept Comp Sci, New Orleans, LA 70125 USA
来源
CANCER INFORMATICS | 2016年 / 15卷
基金
美国国家卫生研究院;
关键词
DNA copy number alterations; RNA-seq; normalization;
D O I
10.4137/CIN.S39781
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: DNA copy number alteration is common in many cancers. Studies have shown that insertion or deletion of DNA sequences can directly alter gene expression, and significant correlation exists between DNA copy number and gene expression. Data normalization is a critical step in the analysis of gene expression generated by RNA-seq technology. Successful normalization reduces/removes unwanted nonbiological variations in the data, while keeping meaningful information intact. However, as far as we know, no attempt has been made to adjust for the variation due to DNA copy number changes in RNA-seq data normalization. Results: In this article, we propose an integrated approach for RNA-seq data normalization. Comparisons show that the proposed normalization can improve power for downstream differentially expressed gene detection and generate more biologically meaningful results in gene profiling. In addition, our findings show that due to the effects of copy number changes, some housekeeping genes are not always suitable internal controls for studying gene expression. Conclusions: Using information from DNA copy number, integrated approach is successful in reducing noises due to both biological and nonbiological causes in RNA-seq data, thus increasing the accuracy of gene profiling.
引用
收藏
页码:129 / 141
页数:13
相关论文
共 50 条
  • [41] Analytic Pearson residuals for normalization of single-cell RNA-seq UMI data
    Jan Lause
    Philipp Berens
    Dmitry Kobak
    Genome Biology, 22
  • [42] Novel small RNA spike-in oligonucleotides enable absolute normalization of small RNA-Seq data
    Lutzmayer, Stefan
    Enugutti, Balaji
    Nodine, Michael D.
    SCIENTIFIC REPORTS, 2017, 7
  • [43] Erratum to: An iteration normalization and test method for differential expression analysis of RNA-seq data
    Yan Zhou
    Nan Lin
    Baoxue Zhang
    BioData Mining, 7
  • [44] Novel small RNA spike-in oligonucleotides enable absolute normalization of small RNA-Seq data
    Stefan Lutzmayer
    Balaji Enugutti
    Michael D. Nodine
    Scientific Reports, 7
  • [46] SCell: integrated analysis of single-cell RNA-seq data
    Diaz, Aaron
    Liu, Siyuan J.
    Sandoval, Carmen
    Pollen, Alex
    Nowakowski, Tom J.
    Lim, Daniel A.
    Kriegstein, Arnold
    BIOINFORMATICS, 2016, 32 (14) : 2219 - 2220
  • [47] How does normalization impact RNA-seq disease diagnosis?
    Han, Henry
    Men, Ke
    JOURNAL OF BIOMEDICAL INFORMATICS, 2018, 85 : 80 - 92
  • [48] Evaluation of Normalization Methods for RNA-Seq Gene Expression Estimation
    Wu, Po-Yen
    Phan, John H.
    Zhou, Fengfeng
    Wang, May D.
    2011 IEEE INTERNATIONAL CONFERENCE ON BIOINFORMATICS AND BIOMEDICINE WORKSHOPS, 2011, : 50 - 57
  • [49] A combined approach with gene-wise normalization improves the analysis of RNA-seq data in human breast cancer subtypes
    Li, Xiaohong
    Rouchka, Eric C.
    Brock, Guy N.
    Yan, Jun
    O'Toole, Timothy E.
    Tieri, David A.
    Cooper, Nigel G. F.
    PLOS ONE, 2018, 13 (08):
  • [50] Dimensionality Reduction of RNA-Seq Data
    Al-Turaiki, Isra
    INTERNATIONAL JOURNAL OF COMPUTER SCIENCE AND NETWORK SECURITY, 2021, 21 (03): : 31 - 36