Evidence map›Paper›PMID 36478959›Full record

ArticleNAR genomics and bioinformatics2022

Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing.

Alysha S Taylor, Dinis Barros, Nastassia Gobet, Thierry Schuepbach, Branduff McAllister, Lorene Aeschbach, Emma L Randall, Evgeniya Trofimenko, Eleanor R Heuchan, Paula Barszcz and 10 more

Open access · goldAbstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
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

8 citing papers in PubMed, 14 citations in OpenAlex.

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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

20 authors at 8 institutions in 4 countries.

Alysha S TaylorUK Dementia Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.ORCID https://orcid.org/0000-0001-5074-6618
Dinis BarrosCentre for Integrative Genomics, University of Lausanne, Bâtiment Génopode, 1015 Lausanne, Switzerland.
Nastassia GobetCentre for Integrative Genomics, University of Lausanne, Bâtiment Génopode, 1015 Lausanne, Switzerland.ORCID https://orcid.org/0000-0002-6305-0844
Thierry SchuepbachVital-IT Group, Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland.ORCID https://orcid.org/0000-0002-2472-4607
Branduff McAllisterMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff CF24 4HQ, UK.ORCID https://orcid.org/0000-0001-6308-2136
Lorene AeschbachCentre for Integrative Genomics, University of Lausanne, Bâtiment Génopode, 1015 Lausanne, Switzerland.
Emma L RandallUK Dementia Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.ORCID https://orcid.org/0000-0002-2112-7751
Evgeniya TrofimenkoCentre for Integrative Genomics, University of Lausanne, Bâtiment Génopode, 1015 Lausanne, Switzerland.ORCID https://orcid.org/0000-0003-4910-5324
Eleanor R HeuchanUK Dementia Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.ORCID https://orcid.org/0000-0002-7629-0070
Paula BarszczCentre for Integrative Genomics, University of Lausanne, Bâtiment Génopode, 1015 Lausanne, Switzerland.
Marc CiosiSchool of Molecular Biosciences, College of Medical, Veterinary and Life Sciences, Davidson Building, University of Glasgow, Glasgow, G12 8QQ, UK.ORCID https://orcid.org/0000-0002-7663-4080
Joanne MorganMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff CF24 4HQ, UK.ORCID https://orcid.org/0000-0003-3091-0040
Nathaniel J Hafford-TearUCL Institute of Ophthalmology, 11-43 Bath Street, London, EC1V 9EL UK.ORCID https://orcid.org/0000-0001-8564-5198
Alice E DavidsonUCL Institute of Ophthalmology, 11-43 Bath Street, London, EC1V 9EL UK.ORCID https://orcid.org/0000-0002-1816-6151
Thomas H MasseyMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff CF24 4HQ, UK.ORCID https://orcid.org/0000-0002-9804-2131
Darren G MoncktonSchool of Molecular Biosciences, College of Medical, Veterinary and Life Sciences, Davidson Building, University of Glasgow, Glasgow, G12 8QQ, UK.ORCID https://orcid.org/0000-0002-8298-8264
Lesley JonesMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff CF24 4HQ, UK.ORCID https://orcid.org/0000-0002-3007-4612
Registry Investigators Of The European Huntington's Disease Network
Ioannis XenariosCentre for Integrative Genomics, University of Lausanne, Bâtiment Génopode, 1015 Lausanne, Switzerland.ORCID https://orcid.org/0000-0002-3413-6841
Vincent DionUK Dementia Research Institute, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK.ORCID https://orcid.org/0000-0003-4953-7637
University of Lausanne · CHUK Dementia Research Institute · GBCardiff University · GBUniversity College London · GBUniversity of Glasgow · GBCentre National de la Recherche Scientifique · FRMassachusetts General Hospital · USSIB Swiss Institute of Bioinformatics · CH

Funding

Medical Research Council MR/L010305/1Medical Research Council MR/P001629/1Medical Research Council MR/S031820/1
6 · The paper itself

Abstract

Targeted DNA sequencing approaches will improve how the size of short tandem repeats is measured for diagnostic tests and preclinical studies. The expansion of these sequences causes dozens of disorders, with longer tracts generally leading to a more severe disease. Interrupted alleles are sometimes present within repeats and can alter disease manifestation. Determining repeat size mosaicism and identifying interruptions in targeted sequencing datasets remains a major challenge. This is in part because standard alignment tools are ill-suited for repetitive and unstable sequences. To address this, we have developed Repeat Detector (RD), a deterministic profile weighting algorithm for counting repeats in targeted sequencing data. We tested RD using blood-derived DNA samples from Huntington's disease and Fuchs endothelial corneal dystrophy patients sequenced using either Illumina MiSeq or Pacific Biosciences single-molecule, real-time sequencing platforms. RD was highly accurate in determining repeat sizes of 609 blood-derived samples from Huntington's disease individuals and did not require prior knowledge of the flanking sequences. Furthermore, RD can be used to identify alleles with interruptions and provide a measure of repeat instability within an individual. RD is therefore highly versatile and may find applications in the diagnosis of expanded repeat disorders and in the development of novel therapies.

Identifiers

PMID36478959
PMCPMC9719798
OpenAlexW4311025226

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.