Evidence map›Paper›PMID 35853974›Full record

SynthesisScientific reports2022

Un-biased housekeeping gene panel selection for high-validity gene expression analysis.

Ana I Casas, Ahmed A Hassan, Quirin Manz, Christian Wiwie, Pamela Kleikers, Javier Egea, Manuela G López, Markus List, Jan Baumbach, Harald H H W Schmidt

Abstract readSystematic Review
In one paragraph

Synthesis in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Transcriptome Complexity Disentangled: A Regulatory Molecules Approach.International journal of molecular sciences · 2025
    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

10 authors.

Ana I Casas *Department of Neurology and Center for Translational Neuro- and Behavioural Sciences (C-TNBS), University Clinics Essen, Essen, Germany. anaisabel.casasguijarro@uk-essen.de.
Ahmed A Hassan *Department of Pharmacology & Personalised Medicine, MeHNS, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.
Quirin Manz *Faculty of Mathematics, Informatics and Natural Sciences, University of Hamburg, Hamburg, Germany.
Christian WiwieDepartment of Mathematics and Computer Science, University of Southern Denmark, Odense, Denmark.
Pamela KleikersDepartment of Pharmacology & Personalised Medicine, MeHNS, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.
Javier EgeaMolecular Neuroinflammation and Neuronal Plasticity Research Laboratory, Hospital Universitario Santa Cristina, Instituto de Investigación Sanitaria-Hospital Universitario de la Princesa, Madrid, Spain.
Manuela G LópezDepartamento de Farmacología, Instituto de I+D del Medicamento Teófilo Hernando (ITH), Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.
Markus List *Chair of Experimental Bioinformatics, TUM School of Life Sciences Weihenstephan, Technical University of Munich, Munich, Germany.
Jan Baumbach *Faculty of Mathematics, Informatics and Natural Sciences, University of Hamburg, Hamburg, Germany.
Harald H H W Schmidt *Department of Pharmacology & Personalised Medicine, MeHNS, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands. hschmidt@ppmlab.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differential gene expression normalised to a single housekeeping (HK) is used to identify disease mechanisms and therapeutic targets. HK gene selection is often arbitrary, potentially introducing systematic error and discordant results. Here we examine these risks in a disease model of brain hypoxia. We first identified the eight most frequently used HK genes through a systematic review. However, we observe that in both ex-vivo and in vivo, their expression levels varied considerably between conditions. When applying these genes to normalise expression levels of the validated stroke target gene, inducible Nox4, we obtained opposing results. As an alternative tool for unbiased HK gene selection, software tools exist but are limited to individual datasets lacking genome-wide search capability and user-friendly interfaces. We, therefore, developed the HouseKeepR algorithm to rapidly analyse multiple gene expression datasets in a disease-specific manner and rank HK gene candidates according to stability in an unbiased manner. Using a panel of de novo top-ranked HK genes for brain hypoxia, but not single genes, Nox4 induction was consistently reproduced. Thus, differential gene expression analysis is best normalised against a HK gene panel selected in an unbiased manner. HouseKeepR is the first user-friendly, bias-free, and broadly applicable tool to automatically propose suitable HK genes in a tissue- and disease-dependent manner.

Indexed as

Genes, EssentialHypoxia, BrainAlgorithmsGene ExpressionGene Expression ProfilingHumans

Identifiers

PMID35853974
PMCPMC9296577

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.