About the SeqScreener Gene Edit Confirmation App on Thermo Fisher™ Connect
The SeqScreener Gene Edit Confirmation App (SGC) is an application available through Thermo Fisher™ Connect that can be used to determine the spectrum and frequency of targeted mutations generated in a pool of cells by genome editing tools such as CRISPR-Cas9. Use the SGC app to screen and validate gene editing results obtained using Capillary Electrophoresis (CE) sequencing technology.
The SGC app includes the following features:
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An algorithm that accurately reconstructs the spectrum of Indels from the sequence traces and generates a report
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A report output that identifies the detected Indels and their frequencies
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Detection of designed mutations generated by homologous recombination using a donor template
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Compatibility with both knock-in and knock-out experiments
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Batch import capability
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Pool screening and clonal screening analyses