EventPointer: an effective identification of alternative splicing events using junction arrays

• Published in: BMC genomics Vol. 17; no. 1; p. 467
• Main Authors: Romero, Juan P., Muniategui, Ander, De Miguel, Fernando J., Aramburu, Ander, Montuenga, Luis, Pio, Ruben, Rubio, Angel
• Format: Journal Article
• Language: English
• Published: London BioMed Central 17.06.2016; BioMed Central Ltd; Springer Nature B.V
• Subjects: Algorithms; Alternative Splicing; Analysis; Animal Genetics and Genomics; Biomedical and Life Sciences; Case studies; Cell junctions; Computational Biology - methods; Gene expression; Gene Expression Profiling; Genomics; Junctional complexes (Epithelium); Life Sciences; Methodology; Methodology Article; Microarrays; Microbial Genetics and Genomics; Molecular Sequence Annotation; Oligonucleotide Array Sequence Analysis; Plant Genetics and Genomics; Proteomics; Reproducibility of Results; RNA splicing; Software; Transcriptome; Transcriptomic methods; User-Computer Interface; Alternative splicing; Junction microarrays; Protein domains
• ISSN: 1471-2164; 1471-2164
• DOI: 10.1186/s12864-016-2816-x

Background Alternative splicing (AS) is a major source of variability in the transcriptome of eukaryotes. There is an increasing interest in its role in different pathologies. Before sequencing technology appeared, AS was measured with specific arrays. However, these arrays did not perform well in the detection of AS events and provided very large false discovery rates (FDR). Recently the Human Transcriptome Array 2.0 (HTA 2.0) has been deployed. It includes junction probes. However, the interpretation software provided by its vendor (TAC 3.0) does not fully exploit its potential (does not study jointly the exons and junctions involved in a splicing event) and can only be applied to case–control studies. New statistical algorithms and software must be developed in order to exploit the HTA 2.0 array for event detection. Results We have developed EventPointer, an R package (built under the aroma.affymetrix framework) to search and analyze Alternative Splicing events using HTA 2.0 arrays. This software uses a linear model that broadens its application from plain case–control studies to complex experimental designs. Given the CEL files and the design and contrast matrices, the software retrieves a list of all the detected events indicating: 1) the type of event (exon cassette, alternative 3′, etc.), 2) its fold change and its statistical significance, and 3) the potential protein domains affected by the AS events and the statistical significance of the possible enrichment. Our tests have shown that EventPointer has an extremely low FDR value (only 1 false positive within the tested top-200 events). This software is publicly available and it has been uploaded to GitHub. Conclusions This software empowers the HTA 2.0 arrays for AS event detection as an alternative to RNA-seq: simplifying considerably the required analysis, speeding it up and reducing the required computational power.