Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/16982
Title: Analysis of tiling array expression studies with flexible designs in Bioconductor (waveTiling)
Authors: De Beuf, Kristof
Pipelers, Peter
Andriankaja, Megan
THAS, Olivier 
Inze, Dirk
Crainiceanu, Ciprian
CLEMENT, Lieven 
Issue Date: 2012
Publisher: BIOMED CENTRAL LTD
Source: BMC BIOINFORMATICS, 13, p. Art. N° 234
Abstract: Background: Existing statistical methods for tiling array transcriptome data either focus on transcript discovery in one biological or experimental condition or on the detection of differential expression between two conditions. Increasingly often, however, biologists are interested in time-course studies, studies with more than two conditions or even multiple-factor studies. As these studies are currently analyzed with the traditional microarray analysis techniques, they do not exploit the genome-wide nature of tiling array data to its full potential. Results: We present an R Bioconductor package, waveTiling, which implements a wavelet-based model for analyzing transcriptome data and extends it towards more complex experimental designs. With waveTiling the user is able to discover (1) group-wise expressed regions, (2) differentially expressed regions between any two groups in single-factor studies and in (3) multifactorial designs. Moreover, for time-course experiments it is also possible to detect (4) linear time effects and (5) a circadian rhythm of transcripts. By considering the expression values of the individual tiling probes as a function of genomic position, effect regions can be detected regardless of existing annotation. Three case studies with different experimental set-ups illustrate the use and the flexibility of the model-based transcriptome analysis. Conclusions: The waveTiling package provides the user with a convenient tool for the analysis of tiling array trancriptome data for a multitude of experimental set-ups. Regardless of the study design, the probe-wise analysis allows for the detection of transcriptional effects in both exonic, intronic and intergenic regions, without prior consultation of existing annotation.
Notes: [De Beuf, Kristof; Pipelers, Peter; Thas, Olivier; Clement, Lieven] Univ Ghent, Dept Math Modelling Stat & Bioinformat, B-9000 Ghent, Belgium. [Andriankaja, Megan; Inze, Dirk] Flanders Inst Biotechnol, Dept Plant Syst Biol, Ghent, Belgium. [Andriankaja, Megan; Inze, Dirk] Univ Ghent, Dept Plant Biotechnol & Bioinformat, B-9000 Ghent, Belgium. [Crainiceanu, Ciprian] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD USA. [Clement, Lieven] Katholieke Univ Leuven, Interuniv Inst Biostat & Stat Bioinformat, B-3000 Louvain, Belgium. [Clement, Lieven] Univ Hasselt, B-3000 Louvain, Belgium.
Keywords: Biochemical Research Methods; Biotechnology & Applied Microbiology; Mathematical & Computational Biology
Document URI: http://hdl.handle.net/1942/16982
ISSN: 1471-2105
e-ISSN: 1471-2105
DOI: 10.1186/1471-2105-13-234
ISI #: 000314178600001
Category: A1
Type: Journal Contribution
Validations: ecoom 2014
Appears in Collections:Research publications

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