TRISONIM2020-04-02T15:07:30+02:00

TrisoNIM®

Fetal DNA test in maternal blood for the detection of chromosomal alterations associated with Down, Edwards or Patau syndromes. Using the latest generation massive parallel sequencing (NGS, Next Generation Sequencing) and the application of the NIFTY® algorithm, this study allows estimating the risk of presenting these diseases with a accuracy greater than 99%. In addition, this test provides information about other genetic alterations and also about fetal sex.

TrisoNIM® is the first fetal DNA test performed entirely in Spain.

Why TrisoNIM®?

TrisoNIM® Advance

  • Analyzes all chromosomes.
  • Detects fetal trisomies of chromosomes 21, 13 y 18.
  • Reports of the most frequent sexual anueploides and also fetal sex .
  • Studies 3 microdeletion syndromes: 1p36, 2q33.1 y 5p (cri-du-chat).
  • BGI (NIFTY) software to analyze results, with CE marking for trisomy 21.
  • Detailed calculation of the fetal fraction, using a double algorithm, discarding samples with less than 3.5% of fetal fraction, according to international recommendations.

What requirements must the patient meet to perform TrisoNIM® Advance?

  • Be pregnant for at least 10 weeks confirmed by ultrasound.
  • Single or twin pregnancy.
  • Does not meet the criteria for invasive diagnostics as the first choice.

When is the results report issued?

7 working days from the receipt of the sample.

Reference: PRE1002

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TrisoNIM® Premium

  • Analyzes all chromosomes.
  • Detects fetal trisomies of chromosomes 21, 13 and 18.
  • Reports the most common sex chromosome aneuploidies and fetal sex.
  • Studies seven microdeletion syndromes: 1p36, 1q32-q41 (Van der Wouden), 2q33.1, 5p.15 (cri-du-chat), 10p14-p13 (DiGeorge 2), 11q23-qter (Jacobsen) and 16p12-p11.
  • BGI (NIFTY) software to analyze results, with CE-IVD marking for trisomy 21.
  • Detailed calculation of the fetal fraction, using a double algorithm, discarding samples with less than 3.5% of fetal fraction, according to international recommendations.

What requirements must the patient meet to perform TrisoNIM® Premium?

  • Be pregnant for at least 10 weeks confirmed by ultrasound.
  • Pregnant with only one fetus.
  • Does not meet the criteria for invasive diagnostics as the first choice.

When is the results report issued?

5 working days from the receipt of the sample.

Reference: PRE1001

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TrisoNIM® Excellence

  • Analyzes all chromosomes.
  • Detects fetal trisomies of chromosomes 21, 13 and 18.
  • Reports the most common sex chromosome aneuploidies and fetal sex.
  • Study 38 microdeletion syndromes.
  • BGI (NIFTY) software to analyze results, with CE marking for trisomy 21.
  • Detailed calculation of the fetal fraction, using a double algorithm, discarding samples with less than 3.5% of fetal fraction, according to international recommendations.

What requirements must the patient meet to perform TrisoNIM® Excellence?

  • Be pregnant for at least 10 weeks confirmed by ultrasound.
  • Pregnant with only one fetus.
  • Does not meet the criteria for invasive diagnostics as the first choice.

When is the results report issued?

8 working days from the receipt of the sample.

Reference: PRE1005

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Any doubt about TrisoNIM®?

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