Evidence map›Paper›PMID 32907859›Full record

ArticleLife science alliance2020

multicrispr: gRNA design for prime editing and parallel targeting of thousands of targets.

Aditya M Bhagwat, Johannes Graumann, Rene Wiegandt, Mette Bentsen, Jordan Welker, Carsten Kuenne, Jens Preussner, Thomas Braun, Mario Looso

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. DivergenteLife · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Advances in CRISPR-Cas9 in lineage tracing of model animals.Animal models and experimental medicine · 2025
    Review
  7. Prime Editing of Mouse Primary Neurons.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  8. Review
  9. CRISPR technologies for genome, epigenome and transcriptome editing.Nature reviews. Molecular cell biology · 2024
    Review
  10. Review
  11. Current RNA strategies in treating cardiovascular diseases.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  12. The Development, Optimization and Future of Prime Editing.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Review
  15. Cas9-induced nonhomologous recombination inbioRxiv : the preprint server for biology · 2023
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  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

9 authors at 1 institution in 1 country.

Aditya M BhagwatMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0002-1501-1090
Johannes GraumannMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.
Rene WiegandtMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0002-5921-8413
Mette BentsenMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.
Jordan WelkerMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0003-1017-9449
Carsten KuenneMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0001-8013-5906
Jens PreussnerMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.ORCID 0000-0003-1927-3458
Thomas BraunMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany.
Mario LoosoMax Planck Institute for Heart and Lung Research, Bad Nauheim, Germany mario.looso@mpi-bn.mpg.de.ORCID 0000-0003-1495-9530
Max Planck Institute for Heart and Lung Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting the coding genome to introduce nucleotide deletions/insertions via the CRISPR/Cas9 technology has become a standard procedure. It has quickly spawned a multitude of methods such as prime editing, APEX proximity labeling, or homology directed repair, for which supporting bioinformatics tools are, however, lagging behind. New CRISPR/Cas9 applications often require specific gRNA design functionality, and a generic tool is critically missing. Here, we introduce multicrispr, an R/bioconductor tool, intended to design individual gRNAs and complex gRNA libraries. The package is easy to use; detects, scores, and filters gRNAs on both efficiency and specificity; visualizes and aggregates results per target or CRISPR/Cas9 sequence; and finally returns both genomic ranges and sequences of gRNAs. To be generic, multicrispr defines and implements a genomic arithmetic framework as a basis for facile adaptation to techniques recently introduced such as prime editing or yet to arise. Its performance and design concepts such as target set-specific filtering render multicrispr a tool of choice when dealing with screening-like approaches.

Indexed as

AnimalsClustered Regularly Interspaced Short Palindromic RepeatsComputational BiologyCRISPR-Associated Protein 9CRISPR-Cas SystemsDNA PrimersEndonucleasesGene EditingHumansRNA, Guide, CRISPR-Cas SystemsSoftwareCRISPR-Associated Protein 9DNA PrimersEndonucleasesRNA, Guide, CRISPR-Cas Systems

Identifiers

PMID32907859
PMCPMC7494814
OpenAlexW3083839405

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.