A better way to detect off-target genome changes from base editors

Scientists and physicians can better assess precision genome editing technology using a new method made public today by St.
GEN - Genetic Engineering and Biotechnology News

CHANGE-seq-BE Developed to Allow Scientists to Better Understand Base Editors

CHANGE-seq-BE was developed to enable scientists to better understand base editors, an important class of CRISPR precise genome editors.
EurekAlert!

CHANGE-seq-BE finds off-target changes in the genome from base editors

Find how Circularization for High-throughput Analysis of Nuclease Genome-wide Effects by Sequencing Base Editors ...
News-Medical.Net on MSN

New method can help better assess precision genome editing technology

Scientists and physicians can better assess precision genome editing technology using a new method made public today by St.
MedPage Today on MSN

CAR7 Gene Therapy Shows Promise in T-Cell ALL

The use of base editing to generate universal off-the-shelf CAR T cells induced durable remissions -- up to 36 months in one ...

Base Model M4 MacBook Air: Waste of Money or Best Deal?

Discover if the M4 MacBook Air base model is still a smart choice in 2025. Learn about its performance, storage, and ...
Stars and Stripes

Aviano, Marymount split lopsided matchups

Marymount routed Aviano 53-22 on Friday night. It was the Royals’ first game of the season. The Saints dropped to 0-5. Aviano ...
AZoLifeSciences on MSN

New CHANGE-seq-BE method sharpens safety assessment of CRISPR base editors

Scientists and physicians can better assess precision genome editing technology using a new method made public today by St.

Letters to the Editor: If you get the chance to take a flight on the Goodyear Blimp, take it

An L.A. Times reader describes flying in the Goodyear Blimp as "otherworldly and unusual; it's like nothing else I've ...
eLife

Translational reading frame determines the pathogenicity of C-terminal frameshift deletions in MeCP2: an alternative therapeutic approach

This study offers important insight into the pathogenic basis of intragenic frameshift deletions in the carboxy-terminal domain of MECP2, which account for some Rett syndrome cases, yet similar ...