Genome Editing

The latest group of winning technologies has a little something for everyone—from scientists at the lab bench to those in the clinic and even the classroom.

As the demand for viral vectors rises in new gene therapy approaches, scientists seek ways to optimize their production.

With the help of single-cell sequencing, researchers characterize biological complexity more fully across a multitude of applications.

For the past decade, scientists have relied almost exclusively on CRISPR-Cas systems for genome editing. Now, a smaller but equally efficient nuclease is here to compete. 

In this webinar, Cole Cheng and Connie Rich will discuss the advantages of novel miniaturized plasmids for streamlining preclinical and clinical gene therapy development.

Lipid nanoparticles deliver CRISPR tools directly to lung stem cells, offering new therapeutic avenues for treating genetic diseases.

CASGEVY^® is the first cell therapy based on the CRISPR/Cas9 technology, discoverers of which were awarded the Nobel Prize in Chemistry in 2020.

The microbiome is a dynamic environment that can give researchers the inside scoop on health and disease.

Discover how scientists produce CRISPR-edited cell populations.

Even as CRISPR-based tools become a lab staple, scientists strive to tackle the associated technological challenges to improve their efficacy and safety.   

Discover how scientists engineer systems constructed from bacterial components to investigate and combat antimicrobial resistance.

An optimized version of prime editing technology raises the possibility of a one-time treatment for cystic fibrosis.

Researchers developed a technique, ENGRAM, to keep a running log of the elements that control gene expression in cells. 

In this webinar, Jacob Lamberth will discuss the critical variables and strategies for revolutionizing gene editing experiments.

In this webinar, Jacob Lamberth will discuss the critical variables and strategies for revolutionizing gene editing experiments.

An innovative helper plasmid improves adeno-associated virus quality and infectivity.

There are many techniques that allow scientists to silence a gene, but whether the effect is transient or permanent depends on the type of approach.

From the laboratory to the table, researchers cooked bioengineered fungi into a tempting patty.

In this podcast series, scientists discuss the unique ways they employ synthesized DNA libraries in their research.