Screening for common chromosomal changes in the fetus.
Screening for the most common chromosomal changes.
Generation NIPT
Screening for specific chromosomal aneuploidies of chromosomes 13, 18, 21 which cause known syndromes (Down Syndrome, Edward Syndrome, Patau Syndrome) from 10 weeks onwards
Chromosomes 13, 18, 21, X and Y
Whole Genome Sequencing (Illumina VeriSeq V2)
3 – 5 days from sample arriving at the laboratory*
No
$455
Dedicated Generation NIPT request form required.
Blood
Streck Cell Free DNA BCT 10mL
Dedicated Generation NIPT request form available as a template in most practice management software.
* For majority of samples performed. In some cases a longer turn around time may be observed.
