Fragment Analysis and Sanger Sequencing at Your Convenience

Fragment Analysis and Sanger Sequencing at Your Convenience

About Webinar

Sanger sequencing is used to study a small subset of genes linked to a defined phenotype,confirm next-generation sequencing (NGS) variants, detect minor allele fractions down to 5%, or read contiguous sequences up to 1,000 bases.

Fragment analysis is a powerful technique with simple, straightforward workflows and used in a wide-range of applications, such as detection of mutations, genotyping, identification of short tandem repeats, and gene expression profiling.

The Promega Spectrum Compact CE System offers Sanger sequencing and fragment analysis right on your benchtop. With flexible run scheduling and an easy-to-use interface, you’ll no longer be dependent on sequencing services, batch processing or your colleagues’ schedules.

• Convenient size designed to fit on your benchtop
• Separate consumables cartridges for greater flexibility and reduced consumable waste
• Pre-loaded assays for many commercially available sequencing and STR kits

Sanger sequencing applications for verification of NGS base calls and is an efficient method to confirm successful genome edits in transformed cultures, as well as screen secondary clones for successful editing events using CRISPR-cas9 techniques. Spectrum Compact is designed for use with existing sequencing chemistries using fluorescently labeled dideoxynucleotide triphosphate (ddNTPs) and 4-, 5- and 6-dye STR kits from Promega, and other commercially available kits.

 View Webinar Recording  
 Date - 28th October 2020  /  When - 7 PM 
 

Speaker

                              Dr. Robert S. McLaren​
Senior R&D Scientist at Promega
 

Speaker's Biography：
Bob McLaren received his Bachelors of Science in Microbiology from University College London and his Ph.D. in Biochemistry from the University of Dundee. After pursuing postdoctoral work at UW Madison and NIH he joined Promega in 1998. Since 2001 the main focus of his work at Promega has been on supporting and developing products for the forensics and paternity testing community. In the last 13 years or so he has been one of the lead R&D scientists developing several PowerPlex® multiplex PCR systems for the analysis of forensically relevant STR markers as well as the SwabSolution™, PunchSolution™, and AmpSolution™ reagents that make it possible to perform direct amplification from a variety of sample types and the PowerQuant® System for the quantitation of total human and male DNA in forensic samples prior to STR amplification. Most recently he was the lead R&D scientist at Promega for the joint launch of the Spectrum Compact CE System with Hitachi High Tech. He is now responsible for the Genetic Identity R&D team at Promega.





Moderator

​                                 Manbeena Chawla​
PhD​
Executive Editor​
BioSpectrum