A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models. Issue 3 (25th January 2018)
- Record Type:
- Journal Article
- Title:
- A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models. Issue 3 (25th January 2018)
- Main Title:
- A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models
- Authors:
- Zhou, Weichen
Wang, Yi
Fujino, Masayuki
Shi, Leming
Jin, Li
Li, Xiao‐Kang
Wang, Jiucun - Abstract:
- Abstract : Murine transplantation models are used extensively to research immunological rejection and tolerance. Here we studied both murine heart and liver allograft models using microarray technology. We had difficulty in identifying genes related to acute rejections expressed in both heart and liver transplantation models using two standard methodologies: Student's t test and linear models for microarray data (Limma). Here we describe a new method, standardized fold change (SFC), for differential analysis of microarray data. We estimated the performance of SFC, the t test and Limma by generating simulated microarray data 100 times. SFC performed better than the t test and showed a higher sensitivity than Limma where there is a larger value for fold change of expression. SFC gave better reproducibility than Limma and the t test with real experimental data from the MicroArray Quality Control platform and expression data from a mouse cardiac allograft. Eventually, a group of significant overlapping genes was detected by SFC in the expression data of mouse cardiac and hepatic allografts and further validated with the quantitative RT‐PCR assay. The group included genes for important reactions of transplantation rejection and revealed functional changes of the immune system in both heart and liver of the mouse model. We suggest that SFC can be utilized to stably and effectively detect differential gene expression and to explore microarray data in further studies. Abstract : WeAbstract : Murine transplantation models are used extensively to research immunological rejection and tolerance. Here we studied both murine heart and liver allograft models using microarray technology. We had difficulty in identifying genes related to acute rejections expressed in both heart and liver transplantation models using two standard methodologies: Student's t test and linear models for microarray data (Limma). Here we describe a new method, standardized fold change (SFC), for differential analysis of microarray data. We estimated the performance of SFC, the t test and Limma by generating simulated microarray data 100 times. SFC performed better than the t test and showed a higher sensitivity than Limma where there is a larger value for fold change of expression. SFC gave better reproducibility than Limma and the t test with real experimental data from the MicroArray Quality Control platform and expression data from a mouse cardiac allograft. Eventually, a group of significant overlapping genes was detected by SFC in the expression data of mouse cardiac and hepatic allografts and further validated with the quantitative RT‐PCR assay. The group included genes for important reactions of transplantation rejection and revealed functional changes of the immune system in both heart and liver of the mouse model. We suggest that SFC can be utilized to stably and effectively detect differential gene expression and to explore microarray data in further studies. Abstract : We introduce a new method to analyze microarray data, standardized fold change (SFC). It uses nearby information of one probe in pooled probes and shows better performance than the conventional techniques of Limma and the t test. Further analysis on multiple mouse transplantation models showed a convincing set of 52 overlapping genes, revealing pathway and gene expression changes after cardiac and hepatic allografts. … (more)
- Is Part Of:
- FEBS open bio. Volume 8:Issue 3(2018)
- Journal:
- FEBS open bio
- Issue:
- Volume 8:Issue 3(2018)
- Issue Display:
- Volume 8, Issue 3 (2018)
- Year:
- 2018
- Volume:
- 8
- Issue:
- 3
- Issue Sort Value:
- 2018-0008-0003-0000
- Page Start:
- 481
- Page End:
- 490
- Publication Date:
- 2018-01-25
- Subjects:
- gene expression -- microarray analysis -- murine transplantation model -- standardized fold change
Molecular biology -- Periodicals
Cytology -- Periodicals
Life sciences -- Periodicals
Biological Science Disciplines -- Periodicals
Molecular Biology -- Periodicals
Cell Biology -- Periodicals
Cytology
Life sciences
Molecular biology
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572.805 - Journal URLs:
- http://febs.onlinelibrary.wiley.com/hub/journal/10.1002/(ISSN)2211-5463/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1002/2211-5463.12343 ↗
- Languages:
- English
- ISSNs:
- 2211-5463
- Deposit Type:
- Legaldeposit
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