Efficient, accurate gene editing is critical to your scientific insights
Whether using CRISPR, TALEN, or prime editing technology, gene editing confirmation is critical for harnessing the full power of genome engineering and avoiding a large loss of time and money in performing downstream experimentation whose interpretation may be compromised. Applied Biosystems Sanger sequencing and fragment analysis systems and free SeqScreener Gene Edit Confirmation App enable in-depth, highly accurate genomic confirmation and analysis by users of all skill levels, for genomic alterations of all types (deletion, insertion, single-base changes) using a simple sample-to-answer workflow.
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Highly accurate—single base resolution
Simple workflow—rapid time to results
Flexible—confirm any genomic alteration
Insightful—powerful software with intuitive interface
Webinar: Expanded Frontiers of Gene Editing
In this webinar, Dr. Stephen Jackson, applications senior manager at Thermo Fisher Scientific, discusses the utility of genomic tools in modeling diseases, plants, and animals, as well as the importance of genotypic confirmation of gene edits.
Webinar: Gene editing—the precision tool for tomorrow's treatments
In this webinar series, scientists relate how they harness gene editing technologies to advance their HIV research and rare inherited disease studies including Duchenne muscular dystrophy and MECP2 duplication syndrome.
Augment your phenotypic confirmation with Sanger sequencing & fragment analysis: confidence through genomic confirmation
Unlike phenotypic confirmation, performing genotypic confirmation allows researcher to directly attribute a specific genetic alteration to an experimental outcome, enabling researchers to better understand and confidently interpret their gene editing results across every phase of their workflow. This facilitates the rapid development of more efficient engineering experiments, supports definitive go/no-go decisions on advancing studies relying on engineered cells and/or animal models, and maximizes the safety and efficacy of gene editing-based candidate therapies.
Matching the right genetic analysis tool for the right job
Trust Sanger sequencing and fragment analysis–based methods for rapid gene editing confirmation to more effectively design and optimize gRNAs, screen primary cell pools and single-cell clones, and verify the sequence of the final engineered cells or animal model. Thermo Fisher Scientific offers a range of sequencing and fragment analysis–based methods, cleavage assays, and instruments to meet your speed, throughput, and budgetary needs.
Find the Applied Biosystem’s genetic analyzer that’s right for your lab ›
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TOPO cloning and Sanger sequencing |
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Powerful bioinformatic tools at your fingertips—no specialized expertise needed
Determine the range and frequency of gene edits with the free, intuitive SeqScreener Gene Edit Confirmation App.
- Everything you need all in one software app—analyzing results to generating publication figures
- Easy-to-use—enables quick identification of successful gene knock-outs and knock-ins
- Fast and accurate—robust algorithm calculates editing frequencies and grades the editing outcome
- Flexible viewing—plate-based overviews to individual sequence trace results
White paper: Genetic analysis tools for genome editing workflows
Investigate genomic tools including sequencing, fragment analysis, and other genetic analysis methods for determining the efficiency and accuracy of CRISPR/Cas9 gene edits.
Design, build, deliver, detect and validate—the complete gene editing workflow
Thermo Fisher Scientific offers a complete portfolio of products to design, deliver, and confirm gene edits at the phenotypic and genotypic level so you can confidently engineer your cells—all from one place.
Follow the links to learn more about our product offerings for each workflow step. In many cases, the TrueDesign Genome Editor can be used to design and order reagents for the complete editing experiment.
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Resources
Webinars
Literature
Blog posts
Customer education
For Research Use Only. Not for use in diagnostic procedures.