Evidence map›Paper›PMID 37127601›Full record

ArticleBMC bioinformatics2023

Faster and more accurate pathogenic combination predictions with VarCoPP2.0.

Nassim Versbraegen, Barbara Gravel, Charlotte Nachtegael, Alexandre Renaux, Emma Verkinderen, Ann Nowé, Tom Lenaerts, Sofia Papadimitriou

Abstract read
In one paragraph

Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Benchmark of computational methods to detect digenism in sequencing data.European journal of human genetics : EJHG · 2025
    Review
  4. Article
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  10. Article
  11. Undiagnosed RASopathies in infertile men.Frontiers in endocrinology · 2024
    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

8 authors.

Nassim VersbraegenMachine Learning Group, Université Libre de Bruxelles, 1050, Brussels, Belgium. nversbra@ulb.ac.be.
Barbara GravelMachine Learning Group, Université Libre de Bruxelles, 1050, Brussels, Belgium.
Charlotte NachtegaelMachine Learning Group, Université Libre de Bruxelles, 1050, Brussels, Belgium.
Alexandre RenauxMachine Learning Group, Université Libre de Bruxelles, 1050, Brussels, Belgium.
Emma VerkinderenMachine Learning Group, Université Libre de Bruxelles, 1050, Brussels, Belgium.
Ann NowéInteruniversity Institute of Bioinformatics in Brussels, Université Libre de Bruxelles-Vrije Universiteit Brussel, 1050, Brussels, Belgium.
Tom LenaertsMachine Learning Group, Université Libre de Bruxelles, 1050, Brussels, Belgium.
Sofia PapadimitriouMachine Learning Group, Université Libre de Bruxelles, 1050, Brussels, Belgium.

Funding

European Regional Development Fund 27.002.53.01.4524Fonds De La Recherche Scientifique - FNRS 35276964Fonds De La Recherche Scientifique - FNRS 40005602Fonds De La Recherche Scientifique - FNRS 40008622Fonds Wetenschappelijk Onderzoek I002819NInnoviris 2020 RDIR 55bService Public de Wallonie 2010235-ARIAC
6 · The paper itself

Abstract

backgroundThe prediction of potentially pathogenic variant combinations in patients remains a key task in the field of medical genetics for the understanding and detection of oligogenic/multilocus diseases. Models tailored towards such cases can help shorten the gap of missing diagnoses and can aid researchers in dealing with the high complexity of the derived data. The predictor VarCoPP (Variant Combinations Pathogenicity Predictor) that was published in 2019 and identified potentially pathogenic variant combinations in gene pairs (bilocus variant combinations), was the first important step in this direction. Despite its usefulness and applicability, several issues still remained that hindered a better performance, such as its False Positive (FP) rate, the quality of its training set and its complex architecture.

resultsWe present VarCoPP2.0: the successor of VarCoPP that is a simplified, faster and more accurate predictive model identifying potentially pathogenic bilocus variant combinations. Results from cross-validation and on independent data sets reveal that VarCoPP2.0 has improved in terms of both sensitivity (95% in cross-validation and 98% during testing) and specificity (5% FP rate). At the same time, its running time shows a significant 150-fold decrease due to the selection of a simpler Balanced Random Forest model. Its positive training set now consists of variant combinations that are more confidently linked with evidence of pathogenicity, based on the confidence scores present in OLIDA, the Oligogenic Diseases Database ( https://olida.ibsquare.be ). The improvement of its performance is also attributed to a more careful selection of up-to-date features identified via an original wrapper method. We show that the combination of different variant and gene pair features together is important for predictions, highlighting the usefulness of integrating biological information at different levels.

conclusionsThrough its improved performance and faster execution time, VarCoPP2.0 enables a more accurate analysis of larger data sets linked to oligogenic diseases. Users can access the ORVAL platform ( https://orval.ibsquare.be ) to apply VarCoPP2.0 on their data.

Indexed as

Balanced random forestOligogenic diseasesPathogenicity predictorVariant combinations

Identifiers

PMID37127601
PMCPMC10152795

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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.