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Sample size calculation based on exact test for assessing differential expression analysis in RNA-seq data
被引:28
|作者:
Li, Chung-I
[1
,3
]
Su, Pei-Fang
[2
,3
]
Shyr, Yu
[3
]
机构:
[1] Natl Chiayi Univ, Dept Appl Math, Chiayi, Taiwan
[2] Natl Cheng Kung Univ, Dept Stat, Tainan 70101, Taiwan
[3] Vanderbilt Univ, Ctr Quantitat Sci, Nashville, TN 37235 USA
来源:
BMC BIOINFORMATICS
|
2013年
/
14卷
关键词:
FALSE DISCOVERY RATE;
ISOFORM EXPRESSION;
MICROARRAY;
PACKAGE;
DESIGN;
D O I:
10.1186/1471-2105-14-357
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Background: Sample size calculation is an important issue in the experimental design of biomedical research. For RNA-seq experiments, the sample size calculation method based on the Poisson model has been proposed; however, when there are biological replicates, RNA-seq data could exhibit variation significantly greater than the mean (i.e. over-dispersion). The Poisson model cannot appropriately model the over-dispersion, and in such cases, the negative binomial model has been used as a natural extension of the Poisson model. Because the field currently lacks a sample size calculation method based on the negative binomial model for assessing differential expression analysis of RNA-seq data, we propose a method to calculate the sample size. Results: We propose a sample size calculation method based on the exact test for assessing differential expression analysis of RNA-seq data. Conclusions: The proposed sample size calculation method is straightforward and not computationally intensive. Simulation studies to evaluate the performance of the proposed sample size method are presented; the results indicate our method works well, with achievement of desired power.
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