Evidence map›Paper›PMID 33120976›Full record

ReviewGenes2020

Automatic Gene Function Prediction in the 2020's.

Stavros Makrodimitris, Roeland C H J van Ham, Marcel J T Reinders

Abstract readReview
In one paragraph

Review in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. An informatic workflow for the enhanced annotation of excretory/secretory proteins ofComputational and structural biotechnology journal · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. PANNZER-A practical tool for protein function prediction.Protein science : a publication of the Protein Society · 2022
    Article
  16. RNABMC genomics · 2021
    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

3 authors.

Stavros MakrodimitrisDelft Bioinformatics Lab, Delft University of Technology, 2628XE Delft, The Netherlands.ORCID 0000-0002-3111-4268
Roeland C H J van HamDelft Bioinformatics Lab, Delft University of Technology, 2628XE Delft, The Netherlands.
Marcel J T ReindersDelft Bioinformatics Lab, Delft University of Technology, 2628XE Delft, The Netherlands.ORCID 0000-0002-1148-1562

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current rate at which new DNA and protein sequences are being generated is too fast to experimentally discover the functions of those sequences, emphasizing the need for accurate Automatic Function Prediction (AFP) methods. AFP has been an active and growing research field for decades and has made considerable progress in that time. However, it is certainly not solved. In this paper, we describe challenges that the AFP field still has to overcome in the future to increase its applicability. The challenges we consider are how to: (1) include condition-specific functional annotation, (2) predict functions for non-model species, (3) include new informative data sources, (4) deal with the biases of Gene Ontology (GO) annotations, and (5) maximally exploit the GO to obtain performance gains. We also provide recommendations for addressing those challenges, by adapting (1) the way we represent proteins and genes, (2) the way we represent gene functions, and (3) the algorithms that perform the prediction from gene to function. Together, we show that AFP is still a vibrant research area that can benefit from continuing advances in machine learning with which AFP in the 2020s can again take a large step forward reinforcing the power of computational biology.

Indexed as

Gene OntologyAlgorithmsAmino Acid SequenceComputational BiologyElectronic Data ProcessingMachine LearningModels, BiologicalMolecular Sequence AnnotationProteinsProteinsautomatic function predictionGene Ontologymachine learningprotein representation

Identifiers

PMID33120976
PMCPMC7692357

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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.