A method for analyzing censored survival phenotype with gene expression data
-
Published:2008-10-06
Issue:1
Volume:9
Page:
-
ISSN:1471-2105
-
Container-title:BMC Bioinformatics
-
language:en
-
Short-container-title:BMC Bioinformatics
Author:
Wu Tongtong,Sun Wei,Yuan Shinsheng,Chen Chun-Houh,Li Ker-Chau
Abstract
Abstract
Background
Survival time is an important clinical trait for many disease studies. Previous works have shown certain relationship between patients' gene expression profiles and survival time. However, due to the censoring effects of survival time and the high dimensionality of gene expression data, effective and unbiased selection of a gene expression signature to predict survival probabilities requires further study.
Method
We propose a method for an integrated study of survival time and gene expression. This method can be summarized as a two-step procedure: in the first step, a moderate number of genes are pre-selected using correlation or liquid association (LA). Imputation and transformation methods are employed for the correlation/LA calculation. In the second step, the dimension of the predictors is further reduced using the modified sliced inverse regression for censored data (censorSIR).
Results
The new method is tested via both simulated and real data. For the real data application, we employed a set of 295 breast cancer patients and found a linear combination of 22 gene expression profiles that are significantly correlated with patients' survival rate.
Conclusion
By an appropriate combination of feature selection and dimension reduction, we find a method of identifying gene expression signatures which is effective for survival prediction.
Publisher
Springer Science and Business Media LLC
Subject
Applied Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Structural Biology
Reference33 articles.
1. Golub TR, Slonim DK, Tamayo P, Huard C, Gaasenbeek M, Mesirov JP, Coller H, Loh ML, Downing JR, Caligiuri MA, Bloomfield CD, Lander ES: Molecular classification of cancer: class discovery and class prediction by gene expression monitoring. Science 1999, 286(5439):531–537. 10.1126/science.286.5439.531 2. Perou CM, Sorlie T, Eisen MB, Rijn M, Jeffrey SS, Rees CA, Pollack JR, Ross DT, Johnsen H, Akslen LA, Fluge O, Pergamenschikov A, Williams C, Zhu SX, Lonning PE, Borresen-Dale AL, Brown PO, Botstein D: Molecular portraits of human breast tumours. Nature 2000, 406(6797):747–752. 10.1038/35021093 3. Chen HY, Yu SL, Chen CH, Chang GC, Chen CY, Yuan A, Cheng CL, Wang CH, Terng HJ, Kao SF, Chan WK, Li HN, Liu CC, Singh S, Chen WJ, Chen JJW, Yang PC: A five-gene signature and clinical outcome in non-small-cell lung cancer. N Engl J Med 2007, 356: 11–20. 10.1056/NEJMoa060096 4. Li H, Gui J: Partial Cox regression analysis for high-dimensional microarray gene expression data. Bioinformatics 2004, 21: 3001–3008. 5. Li L, Li H: Dimension reduction methods for microarrays with application to censored survival data. Bioinformatics 2004, 20: 3406–3412. 10.1093/bioinformatics/bth415
Cited by
13 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|