Evidence map›Paper›PMID 31455218›Full record

ArticleBMC bioinformatics2019

An equivalence approach to the integrative analysis of feature lists.

Alex Sánchez-Pla, Miquel Salicrú, Jordi Ocaña

Abstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

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4 · The record

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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.

Alex Sánchez-PlaGenetics, Microbiology and Statistics Department, Universitat de Barcelona, Avinguda Diagonal, 648, Barcelona, 08028, Spain. asanchez@ub.edu.ORCID http://orcid.org/0000-0002-8673-7737
Miquel SalicrúGenetics, Microbiology and Statistics Department, Universitat de Barcelona, Avinguda Diagonal, 648, Barcelona, 08028, Spain.
Jordi OcañaGenetics, Microbiology and Statistics Department, Universitat de Barcelona, Avinguda Diagonal, 648, Barcelona, 08028, Spain.

Funding

Departament d'Universitats, Recerca i Societat de la Informació 622Ministerio de Economía y Competitividad MTM2015-64465-C2-1-R
6 · The paper itself

Abstract

backgroundAlthough a few comparison methods based on the biological meaning of gene lists have been developed, the goProfiles approach is one of the few that are being used for that purpose. It consists of projecting lists of genes into predefined levels of the Gene Ontology, in such a way that a multinomial model can be used for estimation and testing. Of particular interest is the fact that it may be used for proving equivalence (in the sense of "enough similarity") between two lists, instead of proving differences between them, which seems conceptually better suited to the end goal of establishing similarity among gene lists. An equivalence method has been derived that uses a distance-based approach and the confidence interval inclusion principle. Equivalence is declared if the upper limit of a one-sided confidence interval for the distance between two profiles is below a pre-established equivalence limit.

resultsIn this work, this method is extended to establish the equivalence of any number of gene lists. Additionally, an algorithm to obtain the smallest equivalence limit that would allow equivalence between two or more lists to be declared is presented. This algorithm is at the base of an iterative method of graphic visualization to represent the most to least equivalent gene lists. These methods deal adequately with the problem of adjusting for multiple testing. The applicability of these techniques is illustrated in two typical situations: (i) a collection of cancer-related gene lists, suggesting which of them are more reasonable to combine -as claimed by the authors- and (ii) a collection of pathogenesis-based transcript sets, showing which of these are more closely related. The methods developed are available in the goProfiles Bioconductor package.

conclusionsThe method provides a simple yet powerful and statistically well-grounded way to classify a set of genes or other feature lists by establishing their equivalence at a given equivalence threshold. The classification results can be viewed using standard visualization methods. This may be applied to a variety of problems, from deciding whether a series of datasets generating the lists can be combined to the simplification of groups of lists.

Indexed as

AlgorithmsGenesComputer SimulationGene OntologyHumansKidneyNeoplasmsStatistics as TopicEquivalence testsFeature listsFunctional profilesGene lists

Identifiers

PMID31455218
PMCPMC6712676

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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.