Center for Molecular Diagnostics, Genomics and Scientific Research
NIPT
Non-invasive prenatal testing (NIPT) - a tool to ensure your peace of mind.
Find out the risk of major fetal genetic disorders and the gender of the fetus as early as the 10th week of pregnancy.
Sequencing services
We provide services from library preparation to sequencing, according to your needs.
Working with the latest sequencing laboratory equipment and applying strict process quality control standards we ensure the accuracy, flexibility and reliability of your project's sequencing research.
We are the first in Lithuania to perform NIPT research:
>99%
The most accurate screening test for the determination of trisomies of chromosomes 21, 18 and 13 [1-4].
Performed
from
10
week
Determination of the genetic condition of the fetus from the 10th week of pregnancy [1].
procedure
A significantly lower number of invasive procedures in unaffected pregnancies [2-6].
Contact us to discuss your needs and possibilities
- Rose NC, et al. Obstet Gynecol, 2020, doi: 10.1097/AOG.0000000000004084.
- Bianchi DW, et al. N Engl J Med. 2014, doi: 10.1056/NEJMoa1311037
- Gil MM, et al. Ultrasound Obstet Gynecol. 2017, doi: 10.1002/uog.17484.
- Chudova DI, et al. N Engl J Med. 2016 https://pubmed.ncbi.nlm.nih.gov/27406371/
- Platt LD, et al. Am J Obstet Gynecol. 2014, doi: 10.1016/j.ajog.2014.03.065.
- Larion S, et al. Obstet Gynecol. 2014, doi: 10.1097/AOG.0000000000000275
