Evidence map›Paper›PMID 37817002›Full record

ReviewGenetica2023

Approaches to increase the validity of gene family identification using manual homology search tools.

Benjamin J Nestor, Philipp E Bayer, Cassandria G Tay Fernandez, David Edwards, Patrick M Finnegan

Abstract readReview
In one paragraph

Review in Genetica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Genome-Wide Identification ofPlants (Basel, Switzerland) · 2025
    Article
  5. First molecular evidence ofVeterinary world · 2025
    Article
  6. Article
  7. Article
  8. 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

5 authors.

Benjamin J NestorSchool of Biological Sciences, University of Western Australia, Perth, WA, 6009, Australia. benjamin.nestor@research.uwa.edu.au.ORCID https://orcid.org/0000-0001-7814-2867
Philipp E BayerSchool of Biological Sciences, University of Western Australia, Perth, WA, 6009, Australia.ORCID https://orcid.org/0000-0001-8530-3067
Cassandria G Tay FernandezSchool of Biological Sciences, University of Western Australia, Perth, WA, 6009, Australia.ORCID https://orcid.org/0000-0002-8518-1618
David EdwardsSchool of Biological Sciences, University of Western Australia, Perth, WA, 6009, Australia.ORCID https://orcid.org/0000-0001-7599-6760
Patrick M FinneganSchool of Biological Sciences, University of Western Australia, Perth, WA, 6009, Australia.ORCID https://orcid.org/0000-0001-5021-1138

Funding

Australian Research Council DP200101013
6 · The paper itself

Abstract

Identifying homologs is an important process in the analysis of genetic patterns underlying traits and evolutionary relationships among species. Analysis of gene families is often used to form and support hypotheses on genetic patterns such as gene presence, absence, or functional divergence which underlie traits examined in functional studies. These analyses often require precise identification of all members in a targeted gene family. Manual pipelines where homology search and orthology assignment tools are used separately are the most common approach for identifying small gene families where accurate identification of all members is important. The ability to curate sequences between steps in manual pipelines allows for simple and precise identification of all possible gene family members. However, the validity of such manual pipeline analyses is often decreased by inappropriate approaches to homology searches including too relaxed or stringent statistical thresholds, inappropriate query sequences, homology classification based on sequence similarity alone, and low-quality proteome or genome sequences. In this article, we propose several approaches to mitigate these issues and allow for precise identification of gene family members and support for hypotheses linking genetic patterns to functional traits.

Indexed as

GenomeSoftwareBiological EvolutionGene family identificationGenome analysisHomologySequence evolutionSequence similarity

Identifiers

PMID37817002
PMCPMC10692271

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Registered trials

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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.