Back to search

Article

Comprehensive and accelerated mapping of driver mutations through single-nucleotide random mutagenesis of target genes

2025-11-05

Abstract excerpt

Identification of novel driver mutations is crucial for personalized medicine and drug discovery. However, genome-wide studies based solely on patient-derived data cannot confirm the oncogenic potential of detected mutations. Here, we present a genome editing-based method for comprehensive random mutagenesis of target genes. This approach generates cultured cells harboring random single-nucleotide variants (SNVs)...

Topics

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

Identifiers and source

Literature Corpus work
9530e7a1-3417-578b-b832-430b346f8aa5
DOI
10.1101/2025.11.05.686667
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.
Comprehensive and accelerated mapping of driver mutations through single-nucleotide random mutagenesis of target genesDOI 10.1101/2025.11.05.686667
Select a neighboring publication to make it the new centre.