Back to search

Article

Base editing generates substantial off-target single nucleotide variants

2018-11-27

Abstract excerpt

Genome editing tools including CRISPR/Cas9 and base editors hold great promise for correcting pathogenic mutations. Unbiased genome-wide off-target effects of the editing in mammalian cells is required before clinical applications, but determination of the extent of off-target effects has been difficult due to the existence of single nucleotide polymorphisms (SNPs) in individuals. Here, we developed a method named...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
15a94299-f8b4-56f6-b32c-e23d7f9525fa
DOI
10.1101/480145
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Base editing generates substantial off-target single nucleotide variantsDOI 10.1101/480145
Select a neighboring publication to make it the new centre.