Non-invasive fetal chromosomal abnormality prenatal genetic testing Using the world's leading high-throughput sequencing platform to detect fetal DNA fragments in maternal peripheral blood, combined with bioinformatics analysis, to calculate the risk of fetal trisomy 21 (Downs syndrom...

AngelCare® Newborn Genetic Screening AngelCare® Newborn Genetic Screening uses high-throughput sequencing technology to detect 156 common genetic diseases, including genetic metabolic diseases, deafness, thalassemia, duchenne muscular dystrophy and spinal muscular atrophy by collec...

Detection of neonatal genetic metabolic diseases Detection of neonatal genetic metabolic diseases is a revolutionary technology using neonatal population screening-tandem mass spectrometry to analyze amino acids and carnitine/acyl carnitine in blood samples of newborn heel blood samples. A...

Ear Listening®Newborn Deafness Gene Detection Ear Listening®Newborn Deafness Gene Detection The risk of hearing impairment in newborns is assessed by collecting blood samples, extracting DNA for gene sequencing, and combining with bioinformatics analysis. This technique can simulta...

Individualized Drug Guidance Gene Detection Genetic testing to enable more personalized and rational selection of medicines！DNA is extracted from samples, and the related gene loci affecting the efficacy and adverse reactions of drugs are detected. According to the test results, in...

Gene Detection of Monogenetic Hereditary Diseases Gene detection series of single gene hereditary diseases includes panel detection of single gene hereditary diseases, 1,445 types of gene detection and clinical full-exome detection. . Based on scientific and rigorous genomics research and ...