Rossell, David; Attolini, Camille Stephan-Otto; Kroiss, Manuel; Stöcker, Almond Quantifying alternative splicing from paired-end RNA-sequencing data. (English) Zbl 1454.62388 Ann. Appl. Stat. 8, No. 1, 309-330 (2014); corrigendum ibid. 9, No. 3, 1706-1707 (2015). Summary: RNA-sequencing has revolutionized biomedical research and, in particular, our ability to study gene alternative splicing. The problem has important implications for human health, as alternative splicing may be involved in malfunctions at the cellular level and multiple diseases. However, the high-dimensional nature of the data and the existence of experimental biases pose serious data analysis challenges. We find that the standard data summaries used to study alternative splicing are severely limited, as they ignore a substantial amount of valuable information. Current data analysis methods are based on such summaries and are hence suboptimal. Further, they have limited flexibility in accounting for technical biases. We propose novel data summaries and a Bayesian modeling framework that overcome these limitations and determine biases in a nonparametric, highly flexible manner. These summaries adapt naturally to the rapid improvements in sequencing technology. We provide efficient point estimates and uncertainty assessments. The approach allows to study alternative splicing patterns for individual samples and can also be the basis for downstream analyses. We found a severalfold improvement in estimation mean square error compared popular approaches in simulations, and substantially higher consistency between replicates in experimental data. Our findings indicate the need for adjusting the routine summarization and analysis of alternative splicing RNA-seq studies. We provide a software implementation in the R package casper. Cited in 1 ReviewCited in 5 Documents MSC: 62P10 Applications of statistics to biology and medical sciences; meta analysis 62F15 Bayesian inference 62-08 Computational methods for problems pertaining to statistics Keywords:alternative splicing; RNA-Seq; Bayesian modeling; estimation Software:TopHat; SpliceTrap; casper; Soap; survival; BWA; R × Cite Format Result Cite Review PDF Full Text: DOI arXiv Euclid References: [1] Ameur, A., Wetterbom, A., Feuk, L. and Gyllensten, U. (2010). Global and unbiased detection of splice junctions from RNA-seq data. Genome Biol. 11 R34. [2] Blencowe, B. J. (2006). Alternative splicing: New insights from global analyses. Cell 126 37-47. [3] Casella, G. and Berger, R. L. (2001). Statistical Inference , 2nd ed. Duxbury, N. Scituate. · Zbl 0699.62001 [4] Dempster, A. P., Laird, N. M. and Rubin, D. B. (1977). Maximum likelihood from incomplete data via the EM algorithm. J. R. Stat. Soc. Ser. B Stat. 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Nucleic. Acids Res. 34 3150-3160. This reference list is based on information provided by the publisher or from digital mathematics libraries. Its items are heuristically matched to zbMATH identifiers and may contain data conversion errors. In some cases that data have been complemented/enhanced by data from zbMATH Open. This attempts to reflect the references listed in the original paper as accurately as possible without claiming completeness or a perfect matching.