Qualified® test pricing

Qualified® test pricing

Choose the package and options that best fit your needs

Why should you choose the Qualified® prenatal test

  • The Qualified Prenatal Test can be performed as early as the 9th week of pregnancy
  • Qualified Test results are available within 2–3 business days from the date the sample is received by the laboratory

Options of Qualified® prenatal test

Qualified® 90°

Trisomies 21, 18, 13

Sexual aneuploidies

Qualified® 120°

Trisomies 21, 18, 13

Sexual aneuploidies

DiGeorge syndrome

Qualified® 180°

Trisomies 21, 18, 13

Sexual aneuploidies

All deletions and duplications (CNVs) ≥ 7Mb

Qualified® 360°

Aneuploidies (trisomies and monosomies) of all chromosomes (1-22)

Sexual aneuploidies*

All deletions and duplications (CNVs) ≥ 7mb**

Qualified® 6m

Trisomies 21, 18, 13

Sexual aneuploidies

All deletions and duplications (CNVs) ≥ 7Mb

Microdeletions <7mb (6 basic)***

Qualified® 9m

Aneuploidies (trisomies and monosomies) of all chromosores (1-22)

Sexual aneuploidies*

All deletions and duplications (CNVs] ≥ 7mb**

Microdeletions <7mb (9 most common)***

Qualified® 23m

Aneunloidies [trisomies and monosomies] of all chromosomes (1-22)

Sexual aneuploidies*

All deletions and duplications (CNVs) ≥ 7mb**

Microdeletions <7mb (all 23)***

Initiative test (SMA & CF)

Qualified® One

Aneuploidies (trisomies and monosornies) of all chromosomes (1-22)

Sexual aneuploidies*

All deletions and duplications (CNVs) ≥ 7mb**

Microdeletions < 7mb (al 23)***

Initiative test (SMA & CF)

Monogenic diseases 100+**

Qualified® prenatal testing options for twin pregnancy

Qualified® Twin Basic

Trisomies 21, 18, 13

Presence of Y chromosome

Qualified® Twin 360°

Aneuploidies (trisomies and monosomies) of all chromosomes (1-22)

Presence of Y chromosome

All deletions and duplications (CNVs) > 7mb**

Qualified® Vanishing Twin

Trisomies 21, 18, 13

Presence of Y chromosome

Qualified® Signature

The Qualified® SignatureTM option consists of analyzes according to the wishes of pregnant women or the gynecologist's advice, with the assignment of a personal Qualified® SignatureTM advisor who will guide you at every step of the process.

WHY THE QUALIFIED® PRENATAL TEST?

  • More detailed analysis (10-12 million readings per sample)
  • SeQuel™ NIPT Solution is the most advanced 5D platform based on NGS technology
  • The Qualified® prenatal test specificity is 99.9%
  • The Qualified® is the only prenatal test that analyzes all 23 microdeletions 1-7Mb***

The most common sex chromosome aneuploidies are as follows:

  • Turner syndrome (X0)
  • Triple X (XXX)
  • Klinefelter syndrome (XXY)
  • Jacobsen syndrome (XYY)

Some options of Qualified® prenatal test analyze 512 genomic regions of interest, identifying anomalies that, as per current databases, could involve CNVs (Copy Number Variations)

Qualified® One additionally examines 100+ monogenic diseases which are caused by a mutation or change in only one gene. These changes can be inherited from parents or they can happen spontaneously (de novo). These diseases can be inherited in different ways, including autosomal dominant, autosomal recessive and X-linked inheritance, and some examples are cystic fibrosis, tuberous sclerosis, congenital deafness. This type of genetic testing helps in early mutation detection and risk assessment for future offspring in general, not only in the current pregnancy, which is important for planning families and timely medical intervention.

All 23 microdeletions ≤ 7mb:

  • DiGeorge syndrome (22q11.2)
  • 1p36 deletion syndrome
  • Angelman syndrome (15q11.2)
  • Prader-Willi syndrome
  • Cri du Chat (5p-syndrome)
  • Wolf-Hirschhorn syndrome (4p16.3)
  • Jacobsen syndrome (11q23-q24.3)
  • Langer-Giedion syndrome (8q24.11-q24.13)
  • Smith-Magenis syndrome (17p11.2)
  • 2q31.2 deletion syndrome
  • 3q29 deletion syndrome
  • Potocki-Lupski syndrome
  • Alagille syndrome 1
  • 7q11.23 syndrome
  • Miller-Dieker syndrome (17p13.3)
  • Pallister-Killian syndrome
  • 15q11-q13 syndrome
  • 15q14 deletion syndrome
  • Xp21.1-21.2 deletion syndrome
  • 17q11.2 deletion syndrome
  • 17q12 deletion syndrome
  • Koolen-De Vries syndrome
  • Phelan-McDermin syndrome

THE INITIATIVE® IS A PREVENTATIVE SCREENING TEST ON SMA (SPINAL MUSCULAR ATROPHY) TYPES 1, 2, 3 AND 4 AS WELL AS FOR CF (CYSTIC FIBROSIS) INTENDED FOR PREGNANT WOMAN
THE INITIATIVE® TEST CAN BE DONE TOGETHER WITH ANY OPTION OF QUALIFIED® PRENATAL TEST
THE INITIATIVE® TEST IS INCLUDED IN THE PRICE OF THE QUALIFIED® 23m AND QUALIFIED® One OPTIONS

Determining the sex of the baby is included in every test option

Rh factor is included in every test option (valid for pregnant women who are Rh-, if the baby's father is Rh+)

Vanishing Twin is a unique option only for cases where the pregnancy starts as a twin pregnancy and continues as a singleton pregnancy

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