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Case Study

Rapid, Scalable, and Ultra-Sensitive Validation of Allele-Specific Gene Editing Events with genoTYPER-NEXT™

What you'll learn

This case study focuses on a collaboration between GENEWIZ and a large pharmaceutical client to develop a more effective approach for screening engineered cell lines via an automated, interactive NGS-based platform. This powerful technology permits the identification of all classes of genetic disruptions, including mono-allelic, homozygous, and heterozygous biallelic modifications.

 

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For technical support questions, please contact our Next Generation Sequencing team

(877) 436-3949 ext. 1 | NGS@genewiz.com