Evidence map›Paper›PMID 36514890›Full record

ArticleJournal of the Royal Society, Interface2022

Exact Bayesian inference for the detection of graft-mobile transcripts from sequencing data.

Melissa Tomkins, Franziska Hoerbst, Saurabh Gupta, Federico Apelt, Julia Kehr, Friedrich Kragler, Richard J Morris

Open access · hybridAbstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Melissa TomkinsComputational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich NR47UH, UK.ORCID 0000-0002-1593-5023
Franziska HoerbstComputational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich NR47UH, UK.ORCID 0000-0002-1288-7732
Saurabh GuptaMax Planck Institute of Molecular Plant Physiology, Max Planck Institute, Am Mühlenberg 1, Potsdam-Golm 14476, Germany.ORCID 0000-0002-5984-852X
Federico ApeltMax Planck Institute of Molecular Plant Physiology, Max Planck Institute, Am Mühlenberg 1, Potsdam-Golm 14476, Germany.ORCID 0000-0003-3450-9369
Julia KehrInstitute of Plant Science and Microbiology, Universität Hamburg, Ohnhorststrasse 18, Hamburg 22609, Germany.ORCID 0000-0003-3617-9981
Friedrich KraglerMax Planck Institute of Molecular Plant Physiology, Max Planck Institute, Am Mühlenberg 1, Potsdam-Golm 14476, Germany.ORCID 0000-0001-5308-2976
Richard J MorrisComputational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich NR47UH, UK.ORCID 0000-0003-3080-2613
John Innes Centre · GBMax Planck Institute of Molecular Plant Physiology · DEUniversität Hamburg · DE

Funding

Biotechnology and Biological Sciences Research Council BB/P012574/1
6 · The paper itself

Abstract

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.

Indexed as

Gene Expression ProfilingPolymorphism, Single NucleotideBayes TheoremRNA, MessengerSequence Analysis, RNARNA, MessengerBayesian inferencegraftinglong-distance transportmobile mRNARNA-Seq analysissequencing errors

Identifiers

PMID36514890
PMCPMC9748499
OpenAlexW4311368710

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.