DocumentCode :
3318034
Title :
Notice of Retraction
Finding Significant Gene Sets with Weighted Distribution of Gene Expression
Author :
Zuguang Gu ; Chenfeng He ; Jin Wang
Author_Institution :
State Key Lab. of Pharm. Biotechnol., Nanjing Univ., Nanjing, China
fYear :
2011
fDate :
10-12 May 2011
Firstpage :
1
Lastpage :
5
Abstract :
Notice of Retraction

After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.

We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.

The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.

Gene set analysis shows great advantages of finding significant gene categories where genes are involved in relative biological processes or share similar functions. Available tools for gene set analysis are limited for the analysis of microarray experiments with few repeats and also tend to generate false positives for the gene sets containing large number of genes. We present a new method named SGS for finding significant gene sets, in which genes are differentially expressed. The methodology is based on the view that genes being more differentially expressed play more important roles in the gene expression profile. Therefore, a weighted distribution of gene expression is included to calculate the extent of up-regulation and down-regulation of the gene set. Two kinds of cutoffs are introduced to determine the gene sets which are both biological reasonable and statistical significant. Our method can effectively decrease the false positive predictions caused by the large size of gene set. To suit the analysis of microarray data with various experimental designs, including few repeats or multiple conditions, three models were proposed in SGS. The gene expression data from microarray experiments on type II diabetes was analyzed to test the performance of SGS. Under a comparison to GSEA which is one of the most widely used gene set analysis tool, it shows that SGS finds out more gene sets related to oxidative phosphoration and ribosome, and excludes gene sets which do not belong to these two properties. The assessme- t indicates that the new tool performs with higher accuracy and lower false positive rate.
Keywords :
biochemistry; bioinformatics; diseases; genetics; molecular biophysics; false positive rate; gene expression; gene set analysis; gene set down regulation; gene set up regulation; microarray experiments; oxidative phosphoration; ribosome; type II diabetes; weighted distribution; Bioinformatics; Biological system modeling; Diabetes; Gene expression; Genomics; Proteins;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Bioinformatics and Biomedical Engineering, (iCBBE) 2011 5th International Conference on
Conference_Location :
Wuhan
ISSN :
2151-7614
Print_ISBN :
978-1-4244-5088-6
Type :
conf
DOI :
10.1109/icbbe.2011.5780040
Filename :
5780040
Link To Document :
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