Author:
Bengtsson Anders,Bengtsson Henrik
Abstract
Abstract
Background
In a microarray experiment the difference in expression between genes on the same slide is up to 103 fold or more. At low expression, even a small error in the estimate will have great influence on the final test and reference ratios. In addition to the true spot intensity the scanned signal consists of different kinds of noise referred to as background. In order to assess the true spot intensity background must be subtracted. The standard approach to estimate background intensities is to assume they are equal to the intensity levels between spots. In the literature, morphological opening is suggested to be one of the best methods for estimating background this way.
Results
This paper examines fundamental properties of rank and quantile filters, which include morphological filters at the extremes, with focus on their ability to estimate between-spot intensity levels. The bias and variance of these filter estimates are driven by the number of background pixels used and their distributions. A new rank-filter algorithm is implemented and compared to methods available in Spot by CSIRO and GenePix Pro by Axon Instruments. Spot's morphological opening has a mean bias between -47 and -248 compared to a bias between 2 and -2 for the rank filter and the variability of the morphological opening estimate is 3 times higher than for the rank filter. The mean bias of Spot's second method, morph.close.open, is between -5 and -16 and the variability is approximately the same as for morphological opening. The variability of GenePix Pro's region-based estimate is more than ten times higher than the variability of the rank-filter estimate and with slightly more bias. The large variability is because the size of the background window changes with spot size. To overcome this, a non-adaptive region-based method is implemented. Its bias and variability are comparable to that of the rank filter.
Conclusion
The performance of more advanced rank filters is equal to the best region-based methods. However, in order to get unbiased estimates these filters have to be implemented with great care. The performance of morphological opening is in general poor with a substantial spatial-dependent bias.
Publisher
Springer Science and Business Media LLC
Subject
Applied Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Structural Biology
Reference23 articles.
1. Schena M: Microarray Analysis. John Wiley & Sons, New Jersey; 2003.
2. Bengtsson H, Jönsson G, Vallon-Christersson J: Calibration and assessment of channel-specific biases in microarray data with extended dynamical range. BMC Bioinformatics 2004., 5(177):
3. BURLE: Photomultiplier Handbook. BURLE TECHNOLOGIES INC; 1980.
4. Weiss S: Choosing Components for a Microarray Scanner.Hamamatsu Corporation; 2003. [http://www.usa.hamamatsu.com/]
5. AXON: GenePix Pro 6.0, User's Guide & Tutorial.Axon Instruments Inc; 2005. [http://www.axon.com]
Cited by
19 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