Evidence map›Paper›PMID 36269834›Full record

ArticleScience advances2022

Comprehensive analysis and accurate quantification of unintended large gene modifications induced by CRISPR-Cas9 gene editing.

So Hyun Park, Mingming Cao, Yidan Pan, Timothy H Davis, Lavanya Saxena, Harshavardhan Deshmukh, Yilei Fu, Todd Treangen, Vivien A Sheehan, Gang Bao

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

62 citing papers in PubMed, 77 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Review
  6. In vivo systematic detection of the outcomes of CRISPR-Cas9-mediated DNA repair in skeletal muscle stem cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Off-target detection of CRISPR-Cas9 nucleaseSynthetic biology (Oxford, England) · 2026
    Article
  18. Article
  19. Review
  20. Analyzing long-read CRISPR experiments with CRISPRLungo.bioRxiv : the preprint server for biology · 2025
    Article

2 more citing papers are in PubMed but not listed here.

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

10 authors at 2 institutions in 1 country.

So Hyun ParkDepartment of Bioengineering, Rice University, Houston, TX 77030, USA.ORCID 0000-0003-3599-1687
Mingming CaoDepartment of Bioengineering, Rice University, Houston, TX 77030, USA.ORCID 0000-0002-4234-1175
Yidan PanDepartment of Bioengineering, Rice University, Houston, TX 77030, USA.ORCID 0000-0002-9702-8530
Timothy H DavisDepartment of Bioengineering, Rice University, Houston, TX 77030, USA.
Lavanya SaxenaDepartment of Bioengineering, Rice University, Houston, TX 77030, USA.ORCID 0000-0001-6083-4013
Harshavardhan DeshmukhDepartment of Bioengineering, Rice University, Houston, TX 77030, USA.ORCID 0000-0003-1747-0466
Yilei FuDepartment of Computer Science, Rice University, Houston, TX 77005, USA.ORCID 0000-0002-7721-7027
Todd TreangenDepartment of Computer Science, Rice University, Houston, TX 77005, USA.ORCID 0000-0002-3760-564X
Vivien A SheehanEmory University School of Medicine, Atlanta, GA 30322, USA.ORCID 0000-0003-2837-2255
Gang BaoDepartment of Bioengineering, Rice University, Houston, TX 77030, USA.ORCID 0000-0001-5501-554X
Rice University · USEmory University · US

Funding

HBB gene-editing for treating sickle cell diseaseR01HL152314 · NHLBI · RICE UNIVERSITY · PI BAO, GANG · 2020 to 2023
$2.5M
Addressing safety issues by quantify large deletions and chromosomal rearrangements in HBB gene editingOT2HL154977 · NHLBI · RICE UNIVERSITY · PI BAO, GANG · 2020 to 2020
$1.2M
NHLBI NIH HHS OT2 HL154977NHLBI NIH HHS R01 HL152314
6 · The paper itself

Abstract

Most genome editing analyses to date are based on quantifying small insertions and deletions. Here, we show that CRISPR-Cas9 genome editing can induce large gene modifications, such as deletions, insertions, and complex local rearrangements in different primary cells and cell lines. We analyzed large deletion events in hematopoietic stem and progenitor cells (HSPCs) using different methods, including clonal genotyping, droplet digital polymerase chain reaction, single-molecule real-time sequencing with unique molecular identifier, and long-amplicon sequencing assay. Our results show that large deletions of up to several thousand bases occur with high frequencies at the Cas9 on-target cut sites on the

Indexed as

CRISPR-Cas SystemsGene EditingCell LineHematopoietic Stem CellsHumansProgrammed Cell Death 1 ReceptorProgrammed Cell Death 1 Receptor

Identifiers

PMID36269834
PMCPMC9586483
OpenAlexW4307044394

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.