Evidence map›Paper›PMID 37228752›Full record

ArticleCell genomics2023

Resolution of structural variation in diverse mouse genomes reveals chromatin remodeling due to transposable elements.

Ardian Ferraj, Peter A Audano, Parithi Balachandran, Anne Czechanski, Jacob I Flores, Alexander A Radecki, Varun Mosur, David S Gordon, Isha A Walawalkar, Evan E Eichler and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
28.6field-weighted citation impact, top 1% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Structural Variation and Its Roles in Plant Genomes.Plants (Basel, Switzerland) · 2026
    Review
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  16. Low-coverage whole-genome sequencing facilitates accurate and cost-effective haplotype reconstruction in complex mouse crosses.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Article
  17. MoG+3.0: expanded structural variant visualization and integration of genomic data from five newly analyzed mouse strains.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Article
  18. Article
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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

12 authors at 3 institutions in 1 country.

Ardian FerrajDepartment of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, CT 06032, USA.
Peter A AudanoThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Parithi BalachandranThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Anne CzechanskiThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Jacob I FloresThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Alexander A RadeckiDepartment of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, CT 06032, USA.
Varun MosurThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
David S GordonHoward Hughes Medical Institute and Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
Isha A WalawalkarDepartment of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, CT 06032, USA.
Evan E EichlerHoward Hughes Medical Institute and Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
Laura G ReinholdtThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Christine R BeckDepartment of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, CT 06032, USA.
Jackson Laboratory · USHoward Hughes Medical Institute · USUniversity of Connecticut · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI Paul Robson · 1985 to 2026
$61.9M
Sequence and Assembly of Segmental DuplicationsR01HG002385 · NHGRI · UNIVERSITY OF WASHINGTON · PI Evan Eichler · 2001 to 2026
$13.3M
Resources for Comparative Mendelian Disease GenomicsR24OD021325 · OD · JACKSON LABORATORY · PI BERGSTROM, DAVID ERIC, REINHOLDT, LAURA G · 2016 to 2023
$6.5M
Repetitive sequences drive genome variation and plasticityR35GM133600 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Christine R Beck · 2019 to 2026
$3.0M
The UConn/JAX-GM Training Program in Genomic ScienceT32HG010463 · NHGRI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Mark D ADAMS, Christine R Beck · 2020 to 2026
$1.5M
Summer Undergraduate Research Fellowship in the Molecular Biology and Genomics of Human CancerR25CA233420 · NCI · JACKSON LABORATORY · PI Jeffrey Hsu-Min Chuang, Sarah Wojiski · 2019 to 2026
$866k
NCI NIH HHS P30 CA034196NCI NIH HHS R25 CA233420NHGRI NIH HHS R01 HG002385NHGRI NIH HHS T32 HG010463NIGMS NIH HHS R35 GM133600NIH HHS R24 OD021325
6 · The paper itself

Abstract

Diverse inbred mouse strains are important biomedical research models, yet genome characterization of many strains is fundamentally lacking in comparison with humans. In particular, catalogs of structural variants (SVs) (variants ≥ 50 bp) are incomplete, limiting the discovery of causative alleles for phenotypic variation. Here, we resolve genome-wide SVs in 20 genetically distinct inbred mice with long-read sequencing. We report 413,758 site-specific SVs affecting 13% (356 Mbp) of the mouse reference assembly, including 510 previously unannotated coding variants. We substantially improve the

Indexed as

chromatin accessibilitycollaborative crosseffects of structural variationembryonic stem cellsinbred micetransposable elementslong read sequencingmouse genomicsstructural variationwhole genome assembly

Identifiers

PMID37228752
PMCPMC10203049
OpenAlexW4362633699

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.