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Exact Bayesian inference for the detection of graft-mobile transcripts from sequencing data.
Tomkins, Melissa; Hoerbst, Franziska; Gupta, Saurabh; Apelt, Federico; Kehr, Julia; Kragler, Friedrich; Morris, Richard J.
Afiliação
  • Tomkins M; Computational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich NR47UH, UK.
  • Hoerbst F; Computational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich NR47UH, UK.
  • Gupta S; Max Planck Institute of Molecular Plant Physiology, Max Planck Institute, Am Mühlenberg 1, Potsdam-Golm 14476, Germany.
  • Apelt F; Max Planck Institute of Molecular Plant Physiology, Max Planck Institute, Am Mühlenberg 1, Potsdam-Golm 14476, Germany.
  • Kehr J; Institute of Plant Science and Microbiology, Universität Hamburg, Ohnhorststrasse 18, Hamburg 22609, Germany.
  • Kragler F; Max Planck Institute of Molecular Plant Physiology, Max Planck Institute, Am Mühlenberg 1, Potsdam-Golm 14476, Germany.
  • Morris RJ; Computational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich NR47UH, UK.
J R Soc Interface ; 19(197): 20220644, 2022 12.
Article em En | MEDLINE | ID: mdl-36514890
The long-distance transport of messenger RNAs (mRNAs) has been shown to be important for several developmental processes in plants. A popular method for identifying travelling mRNAs is to perform RNA-Seq on grafted plants. This approach depends on the ability to correctly assign sequenced mRNAs to the genetic background from which they originated. The assignment is often based on the identification of single-nucleotide polymorphisms (SNPs) between otherwise identical sequences. A major challenge is therefore to distinguish SNPs from sequencing errors. Here, we show how Bayes factors can be computed analytically using RNA-Seq data over all the SNPs in an mRNA. We used simulations to evaluate the performance of the proposed framework and demonstrate how Bayes factors accurately identify graft-mobile transcripts. The comparison with other detection methods using simulated data shows how not taking the variability in read depth, error rates and multiple SNPs per transcript into account can lead to incorrect classification. Our results suggest experimental design criteria for successful graft-mobile mRNA detection and show the pitfalls of filtering for sequencing errors or focusing on single SNPs within an mRNA.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Perfilação da Expressão Gênica / Polimorfismo de Nucleotídeo Único Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Perfilação da Expressão Gênica / Polimorfismo de Nucleotídeo Único Idioma: En Ano de publicação: 2022 Tipo de documento: Article