Statistical analysis of MPSS measurements: Application to the study of LPS-activated macrophage gene expression

被引:35
作者
Stolovitzky, GA
Kundaje, A
Held, GA
Duggar, KH
Haudenschild, CD
Zhou, D
Vasicek, TJ
Smith, KD
Aderem, A
Roach, JC
机构
[1] IBM Corp, Computat Biol Ctr, Yorktown Hts, NY 10598 USA
[2] Lynx Therapeut Inc, Hayward, CA 94545 USA
[3] Univ Washington, Seattle, WA 98195 USA
[4] Inst Syst Biol, Seattle, WA 98103 USA
关键词
transcription profiling; noise model;
D O I
10.1073/pnas.0406555102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Massively Parallel Signature Sequencing (MPSS), a recently developed high-throughput transcription profiling technology, has the ability to profile almost every transcript in a sample without requiring prior knowledge of the sequence of the transcribed genes. As is the case with DNA microarrays, effective data analysis depends crucially on understanding how noise affects measurements. We analyze the sources of noise in MPSS and present a quantitative model describing the variability between replicate MPSS assays. We use this model to construct statistical hypotheses that test whether an observed change in gene expression in a pair-wise comparison is significant. This analysis is then extended to the determination of the significance of changes in expression levels measured over the course of a time series of measurements. We apply these analytic techniques to the study of a time series of MPSS gene expression measurements on LPS-stimulated macrophages. To evaluate our statistical significance metrics, we compare our results with published data on macrophage activation measured by using Affymetrix GeneChips.
引用
收藏
页码:1402 / 1407
页数:6
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