pegIT

pegIT automates design of prime editing guide RNAs (pegRNAs) for prime editing by generating pegRNAs that encode user-defined edits for Cas9–reverse transcriptase–mediated precise genomic modifications without inducing double-stranded DNA breaks.


Key Features:

  • Automated pegRNA generation: Generates pegRNAs tailored to user-defined edits to implement specified prime editing outcomes.
  • Dual-function pegRNA handling: Accounts for the dual role of pegRNAs as both guide molecules and reverse-transcription templates.
  • Multiple editing scenario support: Handles multiple editing scenarios simultaneously for varied editing designs.
  • High-throughput design support: Supports large-scale pegRNA design workflows to meet high-throughput requirements.
  • Error reduction: Reduces errors associated with manual pegRNA design by automating complex design steps.

Scientific Applications:

  • Prime editing implementation: Enables design of pegRNAs for precise genomic modifications using prime editing without inducing double-stranded DNA breaks.
  • High-throughput genome editing studies: Facilitates large-scale pegRNA design for high-throughput experimental workflows.
  • Therapeutic development: Supports pegRNA design efforts relevant to development of therapeutic genome-editing strategies.

Methodology:

Automated computational generation of pegRNAs tailored to user-defined edits, accommodating multiple editing scenarios and the dual guide-and-template functionality of pegRNAs to support high-throughput design.

Topics

Details

License:
Not licensed
Cost:
Free of charge
Tool Type:
command-line tool, web application
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Python
Added:
10/28/2021
Last Updated:
10/28/2021

Operations

Publications

Anderson MV, Haldrup J, Thomsen EA, Wolff JH, Mikkelsen JG. pegIT - a web-based design tool for prime editing. Nucleic Acids Research. 2021;49(W1):W505-W509. doi:10.1093/nar/gkab427. PMID:34060619. PMCID:PMC8265180.

PMID: 34060619
PMCID: PMC8265180
Funding: - Lundbeck Foundation: R230-2016-2986, R324-2019-1832

Documentation

Links