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ONE-seq

Nomination assay

SeQure's ONE-seq is a nomination assay for comprehensive identification of all putative on- and off-target effects for your gene editing tool of interest. ONE-seq leverages variant-aware off-target enumeration coupled with in vitro cutting and deep sequencing to enable precise identification of on- and off-target edits across distinct genetic sub-populations. This high-powered assay offers the most comprehensive risk assessment available for gene editing, ensuring unparalleled confidence in your therapeutic development.

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ONE-seq overview

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ONE-seq & ONE-Seq-BE

ONE-seq and ONE-seq-BE allow population-scale, variant-aware, off-target nomination. Candidate off-target enumeration, enrichment, and in vitro cutting combined with NGS enables high sensitivity detection of low frequency off-target events.

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Comprehensive off-target assessment

  • Highly sensitive
  • Population-scale variant assessment

Off-target assessment
Guide RNA selection
IND filings

  • Multiple orthogonal methods
  • Variant effect prediction
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Related nomination assays

Change-seq

Biochemical off-target nomination assay optimized for CRISPR-Cas and base editing applications. Designed to be paired with ONE-seq or ONE-seq-BE as an orthogonal method. 

GUIDE-seq

Orthogonal approach to supplement ONE-seq off-target nomination. Unbiased cell-based off-target editing assay provides a complementary approach to supplement your off-target risk assessment efforts.  

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Featured Resources

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Poster
Base Editor Genomic Safety Assessment
Webpage
CHANGE-seq™
Nomination Assay
ONE-seq for Variant-Aware Therapeutic Guide Selection-One-seq incorporates global human genetic diversity
Poster
ONE-seq™ for Variant-Aware Therapeutic Guide Selection
View all resources
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From early discovery through pre-clinical and clinical development

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Still have questions?

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