Italiano
EnglishHIGH RESOLUTION
FOR SUPERIOR PERFORMANCE
Traditional NIPTs use low-depth sequencing (coverage 0.1X), which limits their detection capabilities tochromosomal abnormalities, because of the limited coverage of the gene regions.
PrenatalGenome employs ultra-high-resolution sequencing with a read depth exceeding 500X—more than 5,000 times greater than traditional NIPTs. This ensures comprehensive coverage of the fetal genome, enablingalso the detection of ~7,000 clinically recognized severe genetic diseases, both inherited or de novo, withgreater reliability and improved performance.