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dc.contributor.author
Siegner, Sebastian
dc.contributor.author
Karasu, Mehmet E.
dc.contributor.author
Schröder, Markus S.
dc.contributor.author
Kontarakis, Zacharias
dc.contributor.author
Corn, Jacob
dc.date.accessioned
2021-04-12T11:19:40Z
dc.date.available
2021-03-14T05:26:04Z
dc.date.available
2021-04-12T11:19:40Z
dc.date.issued
2021-03-02
dc.identifier.issn
1471-2105
dc.identifier.other
10.1186/s12859-021-04034-6
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/474339
dc.identifier.doi
10.3929/ethz-b-000474339
dc.description.abstract
Background The rapid expansion of the CRISPR toolbox through tagging effector domains to either enzymatically inactive Cas9 (dCas9) or Cas9 nickase (nCas9) has led to several promising new gene editing strategies. Recent additions include CRISPR cytosine or adenine base editors (CBEs and ABEs) and the CRISPR prime editors (PEs), in which a deaminase or reverse transcriptase are fused to nCas9, respectively. These tools hold great promise to model and correct disease-causing mutations in animal and plant models. But so far, no widely-available tools exist to automate the design of both BE and PE reagents. Results We developed PnB Designer, a web-based application for the design of pegRNAs for PEs and guide RNAs for BEs. PnB Designer makes it easy to design targeting guide RNAs for single or multiple targets on a variant or reference genome from organisms spanning multiple kingdoms. With PnB Designer, we designed pegRNAs to model all known disease causing mutations available in ClinVar. Additionally, PnB Designer can be used to design guide RNAs to install or revert a SNV, scanning the genome with one CBE and seven different ABE PAM variants and returning the best BE to use. PnB Designer is publicly accessible at http://fgcz-shiny.uzh.ch/PnBDesigner/ Conclusion With PnB Designer we created a user-friendly design tool for CRISPR PE and BE reagents, which should simplify choosing editing strategy and avoiding design complications.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
BioMed Central
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Prime editing
en_US
dc.subject
base editing
en_US
dc.subject
Guide RNA design
en_US
dc.subject
Web application
en_US
dc.title
PnB Designer: a web application to design prime and base editor guide RNAs for animals and plants
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
ethz.journal.title
BMC Bioinformatics
ethz.journal.volume
22
en_US
ethz.journal.issue
1
en_US
ethz.pages.start
101
en_US
ethz.size
12 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.publication.place
London
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02030 - Dep. Biologie / Dep. of Biology::02539 - Institut für Molecular Health Sciences / Institute of Molecular Health Sciences::09635 - Corn, Jacob / Corn, Jacob
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00003 - Schulleitung und Dienste::00022 - Bereich VP Forschung / Domain VP Research::02207 - Functional Genomics Center Zurich / Functional Genomics Center Zurich
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02030 - Dep. Biologie / Dep. of Biology::02539 - Institut für Molecular Health Sciences / Institute of Molecular Health Sciences::09635 - Corn, Jacob / Corn, Jacob
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00003 - Schulleitung und Dienste::00022 - Bereich VP Forschung / Domain VP Research::02207 - Functional Genomics Center Zurich / Functional Genomics Center Zurich
ethz.date.deposited
2021-03-14T05:26:21Z
ethz.source
SCOPUS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2021-04-12T11:19:52Z
ethz.rosetta.lastUpdated
2024-02-02T13:29:36Z
ethz.rosetta.versionExported
true
ethz.COinS
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