Webinar #4: Genome editing workflow facilitated by the Thermo Fisher Scientific portfolio solution
This is the fourth topic in the Applied Biosystems SeqStudio Webinar Series, ‘Sanger sequencing and fragment analysis made easy’.
Genome editing is poised to revolutionize our understanding and control of diverse biological systems. Critical to any genome editing workflow is monitoring the efficiency and accuracy of the steps leading to a designed edit.
In this webinar, we will learn about the portfolio solution offered by Thermo Fisher Scientific for designing, verifying and analyzing the effects of a genome editing experiment. In particular, we will discuss various genetic analysis methods—each has particular strengths—that can be used to evaluate genome editing efficiency.
Other topics in the webinar series include:
- Introduction to SeqStudio applications (#1)
- Detect low-level somatic mutations in FFPE samples using Sanger sequencing (#2)
- Enabling neurological disease research via DNA fragment analysis on the new SeqStudio Genetic Analyzer (#3)
- Cell line authentication using STR analysis (#5)
About the presenter
Steve Jackson, PhD
Product Applications Specialist
Thermo Fisher Scientific
Dr. Jackson has over 10 years of experience in genetic analysis technologies. As a senior member of the genetic analysis R&D team at Thermo Fisher Scientific, he helps develop solutions for the research and healthcare markets, leveraging varied technologies such as capillary electrophoresis, digital PCR, next-generation sequencing and microarray analysis.
Complete the form to register for the webinar.
For Research Use Only. Not for use in diagnostic procedures.