Evidence map›Paper›PMID 38253882›Full record

ArticleNature biotechnology2024

Publisher Correction: Detection of mosaic and population-level structural variants with Sniffles2.

Moritz Smolka, Luis F Paulin, Christopher M Grochowski, Dominic W Horner, Medhat Mahmoud, Sairam Behera, Ester Kalef-Ezra, Mira Gandhi, Karl Hong, Davut Pehlivan and 4 more

Abstract readPublished Erratum
In one paragraph

Article in Nature biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Gene-Pseudogene Inversions as a Hidden Source of Missing Heritability.medRxiv : the preprint server for health sciences · 2025
    Article
  6. Article
  7. mBio · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Moritz Smolka *Human Genome Sequencing Center Baylor College of Medicine, Houston, TX, USA.
Luis F Paulin *Human Genome Sequencing Center Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0003-2567-3773
Christopher M GrochowskiDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Dominic W HornerDepartment of Clinical and Movement Neurosciences, Royal Free Campus, Queen Square Institute of Neurology, University College London, London, UK.ORCID http://orcid.org/0009-0002-1988-3838
Medhat MahmoudHuman Genome Sequencing Center Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0002-2553-4231
Sairam BeheraHuman Genome Sequencing Center Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0002-9047-0203
Ester Kalef-EzraDepartment of Clinical and Movement Neurosciences, Royal Free Campus, Queen Square Institute of Neurology, University College London, London, UK.ORCID http://orcid.org/0000-0002-1297-3315
Mira GandhiPacific Northwest Research Institute (PNRI), Seattle, WA, USA.
Karl HongBionano Genomics, San Diego, CA, USA.
Davut PehlivanDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Sonja W ScholzNeurodegenerative Diseases Research Unit, National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.ORCID http://orcid.org/0000-0002-6623-0429
Claudia M B CarvalhoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0002-2090-298X
Christos ProukakisDepartment of Clinical and Movement Neurosciences, Royal Free Campus, Queen Square Institute of Neurology, University College London, London, UK.ORCID http://orcid.org/0000-0001-6423-6539
Fritz J SedlazeckHuman Genome Sequencing Center Baylor College of Medicine, Houston, TX, USA. Fritz.Sedlazeck@bcm.edu.ORCID http://orcid.org/0000-0001-6040-2691

Funding

Comprehensive Deep Phenotyping and Multi-omics to Develop Clinical and Molecular Biomarkers for MeCP2-related DiseasesK23NS125126 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI Davut Pehlivan · 2022 to 2026
$1.1M
Identification of somatic/ mosaic SV and transposon activity and their crosstalk to DNA epigenetic ModificationsUG3NS132105 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI SEDLAZECK, FRITZ J, WU, TAO · 2023 to 2024
$580k
NINDS NIH HHS K23 NS125126NINDS NIH HHS UG3 NS132105
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID38253882
PMCPMC11260898

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.