SeqScreener Gene Edit Confirmation App

Efficient, accurate gene editing is critical to your scientific insights
 

Take the stress out of analyzing your gene editing sequence alterations. Whether it’s knock-ins, knock-outs, deletions, insertions, or single nucleotide changes, the Applied Biosystems SeqScreener Gene Edit Confirmation (SGC) app is for you.  It’s a free, user-friendly software app that makes gene editing confirmation easy for all your CRISPR-Cas9, TALEN, or prime editor experiments. 

• Intuitive design—easy-to-use software enables users of all skill levels to quickly identify successful gene knock-outs, knock-ins and single base changes.  Flexible viewing options including plate-based overviews, indel histograms, and individual sequence traces.
• Fast and accurate—robust algorithm calculates the range and editing frequencies and grades the editing outcome for each sample in a matter of seconds
• All-in-one—visualize results, analyze data, and generate publication figures using a single software app
• Convenient—available for free on the cloud-based Thermo Fisher Connect Platform.  No software download or install is required.  With batch processing capabilities, up to 2,400 files can be uploaded and analyzed at once.
  
  

Download the brochure➔

Access SeqScreener tool in two easy steps

A Thermo Fisher Scientific account is required but creating an account and/or signing in is free, quick and easy.

1. Launch the SeqScreener Gene Edit Confirmation App  
2. Log in to the Thermo Fisher Connect Platform with your user account.

Don't have an account? Create one today with only your name and email. Other benefits include contracted pricing, online quotes, ability to place and track orders, and earning rewards.

SeqScreener how-to videos