Evidence map›Paper›PMID 42178203›Full record

ArticleBioinformatics (Oxford, England)2026

Clarifying the scope and capabilities of ROTS in differential expression analysis.

Tomi Suomi, Jalmari Kettunen, Taneli Pusa, Laura L Elo

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Tomi SuomiTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, FI-20520, Finland.ORCID 0000-0003-3639-979X
Jalmari KettunenTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, FI-20520, Finland.
Taneli PusaTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, FI-20520, Finland.
Laura L EloTurku Bioscience Centre, University of Turku and Åbo Akademi University, Turku, FI-20520, Finland.ORCID 0000-0001-5648-4532

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

summaryRecently, Anwar et al. introduced a method combining the ROTS reproducibility optimisation procedure with empirical Bayes variance estimation from limma. Here, we clarify several methodological aspects to support accurate interpretation of the results. We emphasise that ROTS is a general reproducibility optimisation framework rather than a single statistical test and demonstrate that benchmarking outcomes in the reported spike-in case studies are highly sensitive to analysis and evaluation choices. Furthermore, our reanalyses of the spike-in datasets do not support the reported conclusions, and we were unable to reproduce the results of the clinical Alzheimer's disease case study. These findings highlight the importance of transparent benchmarking practices and careful interpretation of comparative results. AVAILABILITY AND IMPLEMENTATION: The ROTS package is available through Bioconductor. The reanalyses were performed using the original code, with the minimal additions described in the manuscript.

Indexed as

Computational BiologyGene Expression ProfilingSoftwareAlgorithmsAlzheimer DiseaseBayes TheoremHumansReproducibility of Results

Identifiers

PMID42178203
PMCPMC13248865

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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.