Evidence map›Paper›PMID 42864382›Full record

ArticleEuropean journal of human genetics : EJHG2026

Optimized RNA-seq workflow for routine diagnosis of mitochondrial diseases using aberrant expression analysis and phenotype-driven prioritization.

Lucile Riera-Navarro, Eléonore Birgy, Samira Ait-El-Mkadem Saadi, Alexandre Janin, Annabelle Chaussenot, Sarra Bouri, Konstantina Fragaki, Bruno Francou, Patrick Edery, Elsa Kaphan and 14 more

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Article in European journal of human genetics : EJHG, 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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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

24 authors.

Lucile Riera-NavarroService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France. riera-navarro.l@chu-nice.fr.ORCID http://orcid.org/0009-0001-7906-7931
Eléonore BirgyService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France.
Samira Ait-El-Mkadem SaadiService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France.
Alexandre JaninUF Pathologies Cardiaques Héréditaires, Service de Biochimie et Biologie Moléculaire, LBMMS, Hospices Civils de Lyon, Bron, France.
Annabelle ChaussenotService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France.
Sarra BouriService de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.
Konstantina FragakiService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France.
Bruno FrancouService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France.
Patrick EderyService de Génétique et Centre de Référence Maladies Rares (CRMR) CLAD Sud-Est, CHU de Lyon, Lyon, France.
Elsa KaphanService de Médecine Interne et Immunologie, CHU Conception, Marseille, France.
Gaetan LescaPathophysiology and Genetics of Neuron and Muscle (PNMG), UCBL, CNRS UMR5261 - INSERM, Lyon, France.ORCID http://orcid.org/0000-0001-7691-9492
Fabienne Ory MagneDepartment of Neurology, University Hospital of Toulouse, Toulouse, France.
Pascal CintasCentre de Référence de Pathologie Neuromusculaire, CHU Toulouse Purpan, Toulouse, France.
Julien MaquetDepartment of Internal Medicine, Toulouse University hospital, Toulouse, France.ORCID http://orcid.org/0000-0002-2187-9435
Celia HoebekeReference Center for Inherited Metabolic Diseases, Filière Maladie Rare G2m, APHM, CHU Timone Enfant, Marseille, France.
Aline CanoReference Center for Inherited Metabolic Diseases, Filière Maladie Rare G2m, APHM, CHU Timone Enfant, Marseille, France.
Alain FouilhouxCentre de Référence des Maladies Héréditaires du Métabolisme, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Lyon, France.
Marion Aubert MuccaService de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0002-8638-2630
Olivier PatatService de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.ORCID http://orcid.org/0000-0001-5759-1540
Véronique Paquis-FlucklingerService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France.
Sylvie BannwarthService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France.
Vincent ProcaccioService de Génétique, CHU Angers, Univ Angers, INSERM U1083, CNRS 6015, MITOVASC, Équipe MitoLab, SFR ICAT, Angers, France.
Marco LorenziInria Center of University Côte d'Azur, Epione Research Group, Nice, France.
Cécile RouzierService de Génétique Médicale, Centre de Référence des Maladies Mitochondriales, Hôpital Archet 2, CHU de Nice, Nice, France.

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR 21-PMRB-0006)Centre Hospitalier Universitaire de Nice (Nice University Hospital) 23-AOIP-07
6 · The paper itself

Abstract

Mitochondrial diseases (MD) are the most common inherited metabolic disorders and show marked clinical and genetic heterogeneity. Despite widespread use of whole-exome (WES) and whole-genome sequencing (WGS), nearly half of patients remain without molecular diagnosis, partly due to difficulties in interpreting variants affecting RNA splicing or gene expression. RNA sequencing (RNA-seq) has shown promise in research settings, few studies have evaluated its feasibility in routine clinical diagnostics under technical and financial constraints. We evaluated the implementation of RNA-seq in a routine diagnostic workflow for MD using fibroblasts from 38 patients, including 8 analyzed with a candidate-gene approach and 30 with an untargeted strategy. To optimize the workflow and improve sensitivity in untargeted analyses, we focused on aberrant expression detection using OUTRIDER with complementary analytical strategies, including multiple testing correction restricted to disease-relevant gene sets and Z-score-based outlier detection combined with phenotype-driven prioritization using Human Phenotype Ontology terms. This combined strategy enabled diagnostic performance comparable to previously published studies while optimizing resources. Pathogenicity was confirmed in 75% of targeted cases (6/8). In the untargeted cohort, new molecular diagnoses were established in 13% of patients (4/30), despite fewer samples than typically recommended and minimizing costs. Our study demonstrates that RNA-seq is feasible and clinically informative in a routine diagnostic setting despite analytical and financial constraints. RNA-seq represents a valuable complement to WES/WGS for improving variant interpretation and diagnostic yield in MD. We propose a practical framework for its implementation alongside genome sequencing in routine diagnostics.

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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.