DocumentCode
583247
Title
Significance analysis by minimizing false discovery rate
Author
Bei, Yuanzhe ; Hong, Pengyu
Author_Institution
Comput. Sci. Dept., Brandeis Univ., Waltham, MA, USA
fYear
2012
fDate
4-7 Oct. 2012
Firstpage
1
Lastpage
6
Abstract
False discovery rate (FDR) control is widely practiced to correct for multiple comparisons in selecting statistically significant features from genome-wide datasets. In this paper, we present an advanced significance analysis method called miFDR that minimizes FDR when the number of the required significant features is fixed. We compared our approach with other well-known significance analysis approaches such as Significance Analysis of Microarrays [1-3], the Benjamini-Hochberg approach [4] and the Storey approach [5]. The results of using both simulated data sets and public microarray data sets demonstrated that miFDR is more powerful.
Keywords
biology computing; genomics; lab-on-a-chip; Benjamini-Hochberg approach; Storey approach; false discovery rate; genome-wide datasets; miFDR; microarray data; significance analysis; Gaussian distribution; Heart; Hypertension; Probes; Proteins; Rats; Reactive power; false discovery rate; significant analysis;
fLanguage
English
Publisher
ieee
Conference_Titel
Bioinformatics and Biomedicine (BIBM), 2012 IEEE International Conference on
Conference_Location
Philadelphia, PA
Print_ISBN
978-1-4673-2559-2
Electronic_ISBN
978-1-4673-2558-5
Type
conf
DOI
10.1109/BIBM.2012.6392652
Filename
6392652
Link To Document