Evidence map›Paper›PMID 42816061›Full record

ArticleLupus science & medicine2026

Balancing automation and expertise: real-world evaluation of AI-assisted whole-exome sequencing in lupus-causing genes.

Anastasia-Vasiliki Madenidou, Gillian I Rice, Terence Garner, Sarah Dyball, Ben Parker, Alice Chieng, Adam Stevens, Ian N Bruce, Tracy A Briggs

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Article in Lupus science & medicine, 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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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Anastasia-Vasiliki MadenidouCentre for Musculoskeletal Research, The University of Manchester, Manchester, UK anastasia.madenidou@manchester.ac.uk.ORCID http://orcid.org/0000-0002-7382-9958
Gillian I RiceDivision of Evolution, Infection and Genomic Sciences, The University of Manchester, Manchester, UK.
Terence GarnerDivision of Developmental Biology and Medicine, The University of Manchester, Manchester, UK.
Sarah DyballCentre for Musculoskeletal Research, The University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0001-6201-7391
Ben ParkerKellgren Centre for Rheumatology, Manchester Royal Infirmary, Manchester University NHS Foundation Trust, Manchester, UK.
Alice ChiengDepartment of Rheumatology, Royal Manchester Children's Hospital, Manchester, UK.
Adam StevensDivision of Developmental Biology and Medicine, The University of Manchester, Manchester, UK.
Ian N BruceCentre for Musculoskeletal Research, The University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0003-3047-500X
Tracy A BriggsDivision of Evolution, Infection and Genomic Sciences, The University of Manchester, Manchester, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWhole-exome sequencing (WES) is increasingly used to investigate patients with suspected monogenic forms of systemic lupus erythematosus (SLE) and other systemic autoimmune rheumatic diseases (SARDs). With the increasing use of artificial intelligence (AI)-assisted variant interpretation tools, there is a need to evaluate their real-world utility. In a SARD cohort, we compared the performance of AI-assisted and expert-guided WES analysis strategies in identifying disease-relevant variants within lupus-causing genes.

methodsWe analysed WES data from 120 SARD patients using the same platform, Emedgene. For the AI-assisted analysis, a fully automated phenotype-based variant analysis produced a list of prioritised potentially disease-causing variants for each case, labelled as 'most likely'. For the expert-guided approach, expert-informed filtering criteria were applied. Both the 'most likely' AI-assisted and the expert-informed filtered variants then underwent further manual analysis.

resultsBefore manual analysis, a total of 2906 variants potentially likely to be causative were identified with the Emedgene AI tool (mean 20.8 variants per case), approximately three times fewer than the 8391 variants identified by the expert-guided method (mean 59.9 per case). A comparable number of variants (78 vs 56) in lupus-causing genes were identified at the end of the manual analysis with both methods, including two monogenic cases

conclusionsAI-assisted WES analysis substantially reduced the number of variants requiring manual review without missing the two monogenic cases. These findings support the integration of AI-assisted pipelines into genomic workflows for SLE and other SARDs which has the potential to improve efficiency and scalability of WES.

Indexed as

Artificial IntelligenceExome SequencingLupus Erythematosus, SystemicAutomationFemaleGenetic Predisposition to DiseaseHumansMalePhenotypeRheumatic DiseasesAutoimmune DiseasesAutoimmunityLupus Erythematosus, Systemic

Identifiers

PMID42816061
PMCPMC13630107

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