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The Yourgene QS250, supplied by Yourgene Health performs:

  • Fragment length analysis

  • Accurate Library quantification

  • Enrichment of DNA of interest

  • All with a single piece of equipment

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IONA® Nx, is a screening test that performs:

1. Whole genome analysis to measure the likelihood that a pregnant woman is carrying a fetus with:

Most common trisomies

  • Trisomy 21 (Down’ Syndrome)

  • Trisomy 18 (Edwards’ Syndrome)

  • Trisomy 13 (Patau’s Syndrome)

Autosomal Aneuploidies (AAs)

  • Additional trisomy across the whole-genome

  • All monosomy across the whole-genome

  • Sex Chromosome Aneuploidies (SCAs)

  • 45,X (Turner Syndrome)

  • 47,XXX (Trisomy X)

  • 47,XXY (Klinefelter’s Syndrome)

  • 47,XYY (Jacob’s Syndrome)

 

2. Fetal Sex Determination

Key Features of the IONA® Nx NIPT Workflow

  • Advanced proprietary reagents and software technologies

  • Simple process with minimum instrumentation capital expenditure, suppliers and contract services

  • Designed to offer flexibility (automated or manual) and scalability to suit varying customer needs

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