Evidence map›Paper›PMID 31147705›Full record

ArticleNucleic acids research2019

APERO: a genome-wide approach for identifying bacterial small RNAs from RNA-Seq data.

Simon Leonard, Sam Meyer, Stephan Lacour, William Nasser, Florence Hommais, Sylvie Reverchon

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Identification of Small RNAs inInternational journal of molecular sciences · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. CRISPRi screen for enhancing heterologous α-amylase yield in Bacillus subtilis.Journal of industrial microbiology & biotechnology · 2023
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Microorganisms · 2021
    Review
  19. Article
  20. 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

6 authors at 2 institutions in 1 country.

Simon LeonardUniversité de Lyon, INSA-Lyon, Université Claude Bernard Lyon1, CNRS UMR5240, Laboratoire de Microbiologie, Adaptation, Pathogénie, 11 avenue Jean Capelle, F-69621 Villeurbanne, France.
Sam MeyerUniversité de Lyon, INSA-Lyon, Université Claude Bernard Lyon1, CNRS UMR5240, Laboratoire de Microbiologie, Adaptation, Pathogénie, 11 avenue Jean Capelle, F-69621 Villeurbanne, France.
Stephan LacourUniv. Grenoble Alpes, CNRS, Inria, LiPhy (UMR5588), 38000 Grenoble, France.
William NasserUniversité de Lyon, INSA-Lyon, Université Claude Bernard Lyon1, CNRS UMR5240, Laboratoire de Microbiologie, Adaptation, Pathogénie, 11 avenue Jean Capelle, F-69621 Villeurbanne, France.
Florence HommaisUniversité de Lyon, INSA-Lyon, Université Claude Bernard Lyon1, CNRS UMR5240, Laboratoire de Microbiologie, Adaptation, Pathogénie, 11 avenue Jean Capelle, F-69621 Villeurbanne, France.
Sylvie ReverchonUniversité de Lyon, INSA-Lyon, Université Claude Bernard Lyon1, CNRS UMR5240, Laboratoire de Microbiologie, Adaptation, Pathogénie, 11 avenue Jean Capelle, F-69621 Villeurbanne, France.
Université Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small non-coding RNAs (sRNAs) regulate numerous cellular processes in all domains of life. Several approaches have been developed to identify them from RNA-seq data, which are efficient for eukaryotic sRNAs but remain inaccurate for the longer and highly structured bacterial sRNAs. We present APERO, a new algorithm to detect small transcripts from paired-end bacterial RNA-seq data. In contrast to previous approaches that start from the read coverage distribution, APERO analyzes boundaries of individual sequenced fragments to infer the 5' and 3' ends of all transcripts. Since sRNAs are about the same size as individual fragments (50-350 nucleotides), this algorithm provides a significantly higher accuracy and robustness, e.g., with respect to spontaneous internal breaking sites. To demonstrate this improvement, we develop a comparative assessment on datasets from Escherichia coli and Salmonella enterica, based on experimentally validated sRNAs. We also identify the small transcript repertoire of Dickeya dadantii including putative intergenic RNAs, 5' UTR or 3' UTR-derived RNA products and antisense RNAs. Comparisons to annotations as well as RACE-PCR experimental data confirm the precision of the detected transcripts. Altogether, APERO outperforms all existing methods in terms of sRNA detection and boundary precision, which is crucial for comprehensive genome annotations. It is freely available as an open source R package on https://github.com/Simon-Leonard/APERO.

Indexed as

AlgorithmsGenome, BacterialDatasets as TopicEnterobacteriaceaeEscherichia coliHigh-Throughput Nucleotide SequencingInternetRNA, AntisenseRNA, BacterialRNA, MessengerRNA, Small UntranslatedSalmonella entericaSequence Analysis, RNASoftwareRNA, AntisenseRNA, BacterialRNA, MessengerRNA, Small Untranslated

Identifiers

PMID31147705
PMCPMC6735904
OpenAlexW2947620157

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.