Article

Overcoming lentiviral delivery limitations in hard-to-transduce suspension cells for genome-wide CRISPR screening

2025-05-01

Abstract excerpt

<h4>ABSTRACT</h4> Lentiviral vectors are a cornerstone delivery modality of biomedical research, renowned for their ability to stably integrate genetic material into the host genome, enabling sustained transgene expression and long-term genetic manipulation. These properties make them indispensable tools in functional genomics and genome engineering, particularly for delivering molecular components in high-throug...

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Literature Corpus work: 6ddb6851-44ca-5811-8ea0-0ca8a53001f2
DOI: 10.1101/2025.05.01.651049

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