Newborn genome screening service that detects major genetic diseases and chromosomal disorders including Wilson disease, ADHD, and congenital hearing loss. Provides early identification of genetic conditions in infants.
Manufactured by
Eone-Diagnomics Genome Center
South Korea
Global NGS Company, EDGCWe provide the value for a healthy lifestyle by suggesting customized healthcare based on genome information.Through genome analysis, we have provided genetic screening tests to help people predict cancer and diseases and to offer personalized healthcare.We have developed cutting-edge diagnostic solutions that empower individuals to make informed health decisions.
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Shenzhen Uni-medica Technology Co., Ltd · China
Next-generation sequencing-based screening for over 165 preventable genetic and metabolic diseases in newborns. Enables early detection, diagnosis, and treatment to reduce disease impact using patented All-in-One PCR amplicon capture technology.
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A comprehensive genetic detection product called 'Bekang' that uses proprietary All-in-One ultra-high coverage PCR amplicon capture technology combined with next-generation sequencing to detect over 165 preventable genetic and metabolic diseases in newborns. It enables early detection, early diagnosis, and early treatment to reduce disease burden in infants.
Trivitron Healthcare Private Limited · India
Specialized screening tests for hereditary and genetic disorders in newborns and populations, utilizing advanced biochemical and molecular techniques for early disease detection.
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