Tech Notes
Improving Electronic Genome Mapping Genome Coverage With CRISPR/Cas9

Discover how CRISPR/Cas9 enhances genome coverage, accuracy, and flexibility in Electronic Genome Mapping (EGM)
EGM has already revolutionized how structural variants and long-range DNA features are detected—but what if you could go even further?
In this technical note, you'll learn how the strategic use of CRISPR/Cas9:
- Provides flexibility to add new tags, to expand genome coverage beyond the limits of traditional nicking protocols
- Enables precise, customizable tagging for increased resolution in regions of high interest
- Improves data quality by minimizing double-strand breaks and proximity errors resulting in longer read lengths
Whether you're working in genome assembly, structural variant analysis, or translational genomics, learn how CRISPR-based enhancements can take your mapping capabilities to the next level.
Download this technical note to learn more!
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Gain confidence in your genomic discoveries from NGS and long-read sequencing (LRS) platforms with a low-cost solution to verify, clarify, and identify structural variant (SV) calls.
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