Evidence map›Paper›PMID 42557338›Full record

ArticleEuropean journal of human genetics : EJHG2026

Detecting pathogenic structural variation in families with undiagnosed rare disease in a national genome project.

Prasun Dutta, Alistair T Pagnamenta, Christelle Robert, Anthony E F McGuigan, Alison Ross, Edward S Tobias, Ruth McGowan, Morad Ansari, David Baty, Jonathan Berg and 15 more

Abstract read
In one paragraph

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Genomics cycle: discover, diagnose, interpret, act.European journal of human genetics : EJHG · 2026
    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

25 authors.

Prasun DuttaCentre for Genomic and Experimental Medicine, MRC Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Alistair T PagnamentaCentre for Human Genetics and NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, Oxfordshire, UK.ORCID http://orcid.org/0000-0001-7334-0602
Christelle RobertCentre for Genomic and Experimental Medicine, MRC Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Anthony E F McGuiganCentre for Human Genetics and NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, Oxfordshire, UK.
Alison RossNorth of Scotland Medical Genetic Service, NHS Grampian, Polwarth Building, Foresterhill, Aberdeen, UK.
Edward S TobiasWest of Scotland Centre for Genomic Medicine, NHS Greater Glasgow & Clyde and University of Glasgow, Queen Elizabeth University Hospital, Glasgow, Scotland, UK.
Ruth McGowanWest of Scotland Centre for Genomic Medicine, Queen Elizabeth University Hospital, Glasgow, Scotland, UK.
Morad AnsariSouth East of Scotland Genetics Service, Western General Hospital, Edinburgh, UK.
David BatyEast of Scotland Regional Genetics Service, NHS Tayside, Ninewells Hospital, Dundee, UK.
Jonathan BergEast of Scotland Regional Genetics Service, NHS Tayside, Ninewells Hospital, Dundee, UK.
Therese BradleyLaboratory Genetics, West of Scotland Centre for Genomic Medicine, Queen Elizabeth University Hospital, Glasgow, Scotland, UK.
Vera CerqueiraLaboratory Genetics, West of Scotland Centre for Genomic Medicine, Queen Elizabeth University Hospital, Glasgow, Scotland, UK.
Austin DiamondSouth East of Scotland Genetics Service, Western General Hospital, Edinburgh, UK.ORCID http://orcid.org/0000-0002-9615-229X
Mihail HalachevBioinformatics Analysis Core, MRC Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0002-4594-4588
Anne LampeSouth East of Scotland Genetics Service, Western General Hospital, Edinburgh, UK.
Alison MeynertBioinformatics Analysis Core, MRC Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0001-5839-1751
Caitlin NewmanEdinburgh Genomics, University of Edinburgh, Edinburgh, UK.
Marian ThomsonEdinburgh Genomics, University of Edinburgh, Edinburgh, UK.
Urmi TrivediEdinburgh Genomics, University of Edinburgh, Edinburgh, UK.
Nicola WilliamsLaboratory Genetics, West of Scotland Centre for Genomic Medicine, Queen Elizabeth University Hospital, Glasgow, Scotland, UK.
Jing YuCentre for Human Genetics and NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, Oxfordshire, UK.
Javier Santoyo-LopezEdinburgh Genomics, University of Edinburgh, Edinburgh, UK.ORCID http://orcid.org/0000-0003-1988-5059
Zosia MiedzybrodzkaNorth of Scotland Medical Genetic Service, NHS Grampian, Polwarth Building, Foresterhill, Aberdeen, UK.ORCID http://orcid.org/0000-0003-2890-8136
Jenny C Taylor *Centre for Human Genetics and NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, Oxfordshire, UK.ORCID http://orcid.org/0000-0003-3602-5704
Timothy J Aitman *Centre for Genomic and Experimental Medicine, MRC Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK. tim.aitman@ed.ac.uk.ORCID http://orcid.org/0000-0002-7875-4502

Funding

Wellcome Trust
6 · The paper itself

Abstract

Whole-genome sequencing (WGS) projects for rare disease diagnosis typically yield a diagnostic rate of 25-41%, depending on the methods for patient selection and the extent of prior genetic testing. The Scottish Genomes Partnership (SGP) is a collaborative programme using genome sequencing to diagnose rare disease patients with presumed monogenic aetiology in the Scottish NHS. Within SGP, short-read sequencing (SRS) had previously achieved a diagnostic rate of 23% in affected families. To increase diagnostic yield, we applied Oxford Nanopore Technologies (ONT) long-read sequencing (LRS) to a cohort of 24 SGP families (74 individuals) that remained undiagnosed after SRS-based SNV/indel analysis. We also retrospectively reviewed SRS-derived structural variant (SV) calls to assess whether LRS results could have been detected in SRS data. After quality, rarity, panel-based and inheritance-based filtering, 392 candidate SVs were retained across de novo, homozygous recessive, compound heterozygous and X-linked inheritance models, of which 8 overlapped PanelApp diagnostic-grade "green" genes. Pathogenic or likely pathogenic de novo SVs were identified in 3 of 24 families: an AUTS2 inversion, a DLX5/6 locus inversion, and an FN1 deletion. All three SVs were independently confirmed by retrospective SRS re-analysis using SVRare. These findings demonstrate that LRS-based SV analysis, supported by orthogonal SRS re-analysis, can resolve clinically significant SVs in families who remain unsolved after standard rare disease testing.

Indexed as

Genetic TestingGenomic Structural VariationRare DiseasesFemaleGenome, HumanHumansMalePedigreeScotlandWhole Genome Sequencing

Identifiers

PMID42557338
PMCPMC13634035

What OpenQuestion holds

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Registered trials

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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.