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Rainbow Genomics Launches Retinal Dystrophy (Eye Disorders) Test Using Dual Whole-Exome and 300-Gene Deep Sequencing
Dual Sequencing Approach Determines Both Novel Variants Specific to Asian Patients, and Challenging Mutations Not Easily Detected by Routine Sequencing Methods
United states
Healthcare pharmaceuticals industry
Asian patients
Challenging mutations not easily detected
Routine sequencing methods
Hong kong based rainbow genomics
Rainbow dual testing approach
Exome analysis
Eye disorders tested
Rainbow dual
Cone rod dystrophy
Late onset retinal
Enhanceds cone
East asian
South asian
Rainbow genomics
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