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Genomics Solutions:

Splicing variant analysis 

Genetic variants close in promixity to exon-intron junctions have a high chance of perturbing gene function, which could result in disease causation.


To rapidly identify genetic variants that may disrupt splicing, Ranomics has developed a dual-fluorescence based reporter that is compatible with any exon-intron-exon junction of interest. 

Our reporter system is compatible with a variety of readouts:


  • microscopy 

  • fluorescence-activated cell sorting

  • next generation sequencing


Ranomics' splicing reporter system can be adapted to characterize a single variant or thousands of variants in a single, streamlined workflow. 

Get in touch
Let us show you how Ranomics can enable your R&D 

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