Evidence map›Paper›PMID 35643462›Full record

ArticleBMC bioinformatics2022

FragGeneScanRs: faster gene prediction for short reads.

Felix Van der Jeugt, Peter Dawyndt, Bart Mesuere

Abstract read
In one paragraph

Article in BMC bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Article
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  4. Computational function prediction of bacteria and phage proteins.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  5. Article
  6. Article
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  9. MerCat2: a versatileBioinformatics advances · 2024
    Article
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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

3 authors.

Felix Van der JeugtDepartment of Applied Mathematics, Computer Science and Statistics, Ghent University, Ghent, Belgium. unipept@ugent.be.ORCID http://orcid.org/0000-0003-3168-927X
Peter DawyndtDepartment of Applied Mathematics, Computer Science and Statistics, Ghent University, Ghent, Belgium.
Bart MesuereDepartment of Applied Mathematics, Computer Science and Statistics, Ghent University, Ghent, Belgium.

Funding

Research Foundation-Flanders (FWO) 12I5220N
6 · The paper itself

Abstract

backgroundFragGeneScan is currently the most accurate and popular tool for gene prediction in short and error-prone reads, but its execution speed is insufficient for use on larger data sets. The parallelization which should have addressed this is inefficient. Its alternative implementation FragGeneScan+ is faster, but introduced a number of bugs related to memory management, race conditions and even output accuracy.

resultsThis paper introduces FragGeneScanRs, a faster Rust implementation of the FragGeneScan gene prediction model. Its command line interface is backward compatible and adds extra features for more flexible usage. Its output is equivalent to the original FragGeneScan implementation.

conclusionsCompared to the current C implementation, shotgun metagenomic reads are processed up to 22 times faster using a single thread, with better scaling for multithreaded execution. The Rust code of FragGeneScanRs is freely available from GitHub under the GPL-3.0 license with instructions for installation, usage and other documentation ( https://github.com/unipept/FragGeneScanRs ).

Indexed as

AlgorithmsSoftwareMetagenomeMetagenomicsGene predictionHidden markov modelRustShotgun metagenomics

Identifiers

PMID35643462
PMCPMC9148508

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.