ArticleScientific reports2015
RASA: Robust Alternative Splicing Analysis for Human Transcriptome Arrays.
Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Splice Junction Identification using Long Short-Term Memory Neural Networks.Current genomics · 2021Article
- Comparison of RNA-seq and microarray platforms for splice event detection using a cross-platform algorithm.BMC genomics · 2018Article
- The Usage of Exon-Exon Splice Junctions for the Detection of Alternative Splicing using the REIDS model.Scientific reports · 2018Article
- RNA sequencing and transcriptome arrays analyses show opposing results for alternative splicing in patient derived samples.BMC genomics · 2017Article
- A random effects model for the identification of differential splicing (REIDS) using exon and HTA arrays.BMC bioinformatics · 2017Article
- Comparative evaluation of isoform-level gene expression estimation algorithms for RNA-seq and exon-array platforms.Briefings in bioinformatics · 2017Article
- Genomics of injury: The Glue Grant experience.The journal of trauma and acute care surgery · 2015Article
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Authors and funding
4 authors.
Funding
Abstract
Human transcriptome arrays (HTA) have recently been developed for high-throughput alternative splicing analysis by measuring signals not only from exons but also from exon-exon junctions. Effective use of these rich signals requires the development of computational methods for better gene and alternative splicing analyses. In this work, we introduce a computational method, Robust Alternative Splicing Analysis (RASA), for the analysis of the new transcriptome arrays by effective integration of the exon and junction signals. To increase robustness, RASA calculates the expression of each gene by selecting exons classified as not alternatively spliced. It then identifies alternatively spliced exons that are supported by both exon and junction signals to reduce the false positives. Finally, it detects additional alternative splicing candidates that are supported by only exon signals because the signals from the corresponding junctions are not well detected. RASA was demonstrated with Affymetrix HTAs and its performance was evaluated with mRNA-Seq and RT-PCR. The validation rate is 52.4%, which is a 60% increase when compared with previous methods that do not use selected exons for gene expression calculation and junction signals for splicing detection. These results suggest that RASA significantly improves alternative splicing analyses on HTA platforms.
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