Birth Defect
Disease Susceptibility
Personalized Medicine
DNA Fingerprinting
Variety Identification
Genetic Quality Assessment
Loci confirmation and evaluation
Confirmation of product development content and indicators
Complete gene sequence collection, bioinformatics analysis, primer/probe design, primer/probe synthesis, artificial synthesis of gene fragments
Complete the screening and optimization of primers and probes, establish and optimize the reagent system, and complete the preliminary finalization of the kit
Interpretation software development, testing
Sample testing, verification, optimization, and acceptance check of kit products
Microfluidic + KASP
Simple: only 1 time sample addition
Flexible: 1 chip can test 1/2/4 samples
Centrifuge and heat-sealing: 2 mins
Physical division of each reaction hole
No cross infection in loci
Amplification: 1.5 h
Scan: 10 mins
Fractal pseudo-color map
Visible QC
One-click output test report
The detection kit for 23 hereditary deafness-related genes developed on the basis of IMAP platform, can test 23 mutations of GJB2 gene, SLC26A4 gene, mitochondria 12SrRNA and GJB3 gene in whole blood or filter paper dried blood spot sample, with the coverage for 4 genes related to hereditary deafness up to 90% above.