Evidence map›Paper›PMID 35373735›Full record

ArticleeLife2022

Precise in vivo functional analysis of DNA variants with base editing using ACEofBASEs target prediction.

Alex Cornean, Jakob Gierten, Bettina Welz, Juan Luis Mateo, Thomas Thumberger, Joachim Wittbrodt

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. 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
2.9field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Advances in Fish Gene Editing.Animals : an open access journal from MDPI · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Molecular therapy. Nucleic acids · 2025
    Review
  6. Article
  7. CRISPR-based functional genomics tools in vertebrate models.Experimental & molecular medicine · 2025
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Zebrafish Congenital Heart Disease Models: Opportunities and Challenges.International journal of molecular sciences · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

6 authors at 2 institutions in 3 countries.

Alex Cornean *Centre for Organismal Studies, Heidelberg University, Heidelberg, Germany.ORCID 0000-0003-3727-7057
Jakob Gierten *Centre for Organismal Studies, Heidelberg University, Heidelberg, Germany.ORCID 0000-0001-8143-1918
Bettina Welz *Centre for Organismal Studies, Heidelberg University, Heidelberg, Germany.
Juan Luis MateoDeparment of Computer Science, University of Oviedo, Oviedo, Spain.ORCID 0000-0001-9902-6048
Thomas ThumbergerCentre for Organismal Studies, Heidelberg University, Heidelberg, Germany.ORCID 0000-0001-8485-457X
Joachim WittbrodtCentre for Organismal Studies, Heidelberg University, Heidelberg, Germany.ORCID 0000-0001-8550-7377
Heidelberg University · DEUniversidad de Oviedo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single nucleotide variants (SNVs) are prevalent genetic factors shaping individual trait profiles and disease susceptibility. The recent development and optimizations of base editors, rubber and pencil genome editing tools now promise to enable direct functional assessment of SNVs in model organisms. However, the lack of bioinformatic tools aiding target prediction limits the application of base editing in vivo. Here, we provide a framework for adenine and cytosine base editing in medaka (

Indexed as

Gene EditingZebrafishAdenineAnimalsCRISPR-Cas SystemsCytosineDNAMutationAdenineCytosineDNAbase editingdevelopmental biologydisease variant validationgeneticsgenomicsmedakaSNVzebrafish

Identifiers

PMID35373735
PMCPMC9033269
OpenAlexW4225695788

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.