Evidence map›Paper›PMID 29241002›Full record

ArticleACS chemical biology2018

The Future of Multiplexed Eukaryotic Genome Engineering.

David B Thompson, Soufiane Aboulhouda, Eriona Hysolli, Cory J Smith, Stan Wang, Oscar Castanon, George M Church

Abstract read
In one paragraph

Article in ACS chemical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Understanding the Dynamics of Blast Resistance in Rice-Journal of fungi (Basel, Switzerland) · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Genome-driven cell engineering review:Essays in biochemistry · 2019
    Review
  20. Synthetic evolution.Nature biotechnology · 2019
    Review
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

7 authors.

David B ThompsonDepartment of Genetics, Harvard Medical School , Boston, Massachusetts, United States.ORCID 0000-0003-2009-4975
Soufiane AboulhoudaDepartment of Genetics, Harvard Medical School , Boston, Massachusetts, United States.
Eriona HysolliDepartment of Genetics, Harvard Medical School , Boston, Massachusetts, United States.
Cory J SmithDepartment of Genetics, Harvard Medical School , Boston, Massachusetts, United States.
Stan WangDepartment of Genetics, Harvard Medical School , Boston, Massachusetts, United States.
Oscar CastanonDepartment of Genetics, Harvard Medical School , Boston, Massachusetts, United States.
George M ChurchDepartment of Genetics, Harvard Medical School , Boston, Massachusetts, United States.ORCID 0000-0003-3535-2076

Funding

Center for Genomically Engineered OrgansRM1HG008525 · NHGRI · HARVARD MEDICAL SCHOOL · PI CHURCH, GEORGE M · 2015 to 2019
$10.2M
Genetics and Genomics PhD Training GrantT32GM096911 · NIGMS · HARVARD MEDICAL SCHOOL · PI KENNEDY, SCOTT G · 2011 to 2020
$2.5M
NHGRI NIH HHS RM1 HG008525NIGMS NIH HHS T32 GM096911
6 · The paper itself

Abstract

Multiplex genome editing is the simultaneous introduction of multiple distinct modifications to a given genome. Though in its infancy, maturation of this field will facilitate powerful new biomedical research approaches and will enable a host of far-reaching biological engineering applications, including new therapeutic modalities and industrial applications, as well as "genome writing" and de-extinction efforts. In this Perspective, we focus on multiplex editing of large eukaryotic genomes. We describe the current state of multiplexed genome editing, the current limits of our ability to multiplex edits, and provide perspective on the many applications that fully realized multiplex editing technologies would enable in higher eukaryotic genomes. We offer a broad look at future directions, covering emergent CRISPR-based technologies, advances in intracellular delivery, and new DNA assembly approaches that may enable future genome editing on a massively multiplexed scale.

Indexed as

AnimalsCRISPR-Associated ProteinsCRISPR-Cas SystemsEndonucleasesEukaryotaGene EditingGenomeHumansRNA, Guide, CRISPR-Cas SystemsCRISPR-Associated ProteinsEndonucleasesRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID29241002
PMCPMC5880278

What OpenQuestion holds

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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.