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Case Study

Detection of Previously Unidentified Structural Variants Involved in Glioblastoma Using PacBio® Sequel Sequencing 

What you'll learn

Glioblastoma is a devastating disease due in part to its often late-stage diagnosis, rapid progression, and poor survival rates. This case study looks at how GENEWIZ utilized the PacBio Sequel long-read technology to help a customer improve detection of structural variants within glioblastoma samples.

 

Generation of thousands of long-reads using PacBio Sequel Single Molecule Real-Time (SMRT) technology

Generation of highly-accurate consensus sequences

Identification of approximately 20,000 structural variants

Future applications

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To learn more about our Whole Genome Sequencing services including long-read technology, visit our Whole Genome Sequencing page.

 

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

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