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Analysis of Whole-Genome Tiling Microarrays

Using whole genome tiling arrays allows us to study the plasticity of the Arabidopsis transcriptome under numerous conditions. The aspects monitored include expression measurements of known genes; detection of transcription factor binding sites; identification of new, previously uncharacterized genes and alternative splicing events; assessing differential expression of known and new genes under abiotic stresses as well as for a number of mutants in proteins required for mRNA capping, splicing, and biogenesis of small RNAs.

Related pages

Machine-learning-based normalization and segmentation methods for tiling array data, including the mSTAD transcript identification algorithm.

The At-TAX resource providing access to whole-genome tiling array data and analysis results for Arabidopsis tissues, developmental stages and abiotic stresses

Supplementary data sets are available from our FTP server.

People specializing in this area

Graduate Students

Jonas Behr

I have been working on methods to efficiently incorporate transcriptome measurements like tiling array data and RNA-Seq data into our gene finding system mGene. Results show substantial improvements in prediction accuracy of protein coding genes compared to ab-initio gene finding methods.

Alumnae and Alumni

Georg Zeller, Ph.D.

I have been developing methods for normalization and segmentation of tiling array data with the aims to i) reduce probe sequence effects on hybridization intensity and ii) in comparison to existing methods more accurately segment transcribed exons out of the intergenic/intronic background.

The normalization and segmentation methods have been applied to 11 Arabidopsis tissues and developmental stages aiming to identify new transcripts. Moreover, based on tiling arrays we globally assessed transcriptome changes upon abiotic stress treatment identifying several hundred new, stress-induced transcripts.

A further subproject is aimed at the identification of alternative splicing events, primarily intron retention events, from tiling array data. We approach this task as a two-step classification problem: First, a classifier is trained to discriminate between exons and introns. Subsequently, introns with a large inclusion probability in some tissue are identified as bona fide candidates for alternative splicing by a second classifier.

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