Evidence map›Paper›PMID 39406499›Full record

ArticleGenome research2024

Characterizing tandem repeat complexities across long-read sequencing platforms with TREAT and

Niccoló Tesi, Alex Salazar, Yaran Zhang, Sven van der Lee, Marc Hulsman, Lydian Knoop, Sanduni Wijesekera, Jana Krizova, Anne-Fleur Schneider, Maartje Pennings and 4 more

Abstract read
In one paragraph

Article in Genome research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Article
  7. Exploring potential mechanisms of an African protective locus for Alzheimer's disease in APOEε4 carriers.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  8. Review
  9. 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

14 authors.

Niccoló Tesi *Section Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands; n.tesi@amsterdamumc.nl a.n.salazar@amsterdamumc.nl h.holstege@amsterdamumc.nl.
Alex Salazar *Section Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.
Yaran ZhangSection Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.
Sven van der LeeSection Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.ORCID 0000-0003-1606-8643
Marc HulsmanSection Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.
Lydian KnoopSection Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.
Sanduni WijesekeraSection Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.
Jana KrizovaSection Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.
Anne-Fleur SchneiderSection Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.
Maartje PenningsDepartment of Genome Diagnostics, Radboud University Medical Center, 6525GA Nijmegen, The Netherlands.
Kristel SleegersComplex Genetics of Alzheimer's Disease Group, Antwerp Center for Molecular Neurology, VIB, Antwerp B-2650, Belgium.
Erik-Jan KamsteegDepartment of Genome Diagnostics, Radboud University Medical Center, 6525GA Nijmegen, The Netherlands.ORCID 0000-0001-6480-1892
Marcel ReindersDelft Bioinformatics Lab, Delft University of Technology, 2628CD Delft, The Netherlands.ORCID 0000-0002-1148-1562
Henne HolstegeSection Genomics of Neurodegenerative Diseases and Aging, Department of Clinical Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC, 1081HV Amsterdam, The Netherlands.ORCID 0000-0002-7688-3087

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tandem repeats (TRs) play important roles in genomic variation and disease risk in humans. Long-read sequencing allows for the accurate characterization of TRs; however, the underlying bioinformatics perspectives remain challenging. We present

Indexed as

High-Throughput Nucleotide SequencingTandem Repeat SequencesAlzheimer DiseaseComputational BiologyGenotypeHumansNanopore SequencingSequence Analysis, DNASoftware

Identifiers

PMID39406499
PMCPMC11610572

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.