Non-invasive Prenatal Testing
High incidence rate of Downโs syndrome are the prominent trends that affect market growth.
WILMINGTON, DELAWARE , UNITED STATES, October 18, 2023 /EINPresswire.com/ — The Global โ๐๐จ๐ง-๐๐ง๐ฏ๐๐ฌ๐ข๐ฏ๐ ๐๐ซ๐๐ง๐๐ญ๐๐ฅ ๐๐๐ฌ๐ญ๐ข๐ง๐ ๐๐๐ซ๐ค๐๐ญโ was valued at US$ 2.1 Billion in 2022. It is projected to advance at a CAGR of 14.8% from 2022 to 2031 to reach more than US$ 8.4 Billion by the end of 2031.
๐๐จ๐ฐ๐ง๐ฅ๐จ๐๐ ๐ ๐๐จ๐ฆ๐ฉ๐ซ๐๐ก๐๐ง๐ฌ๐ข๐ฏ๐ ๐๐๐ฆ๐ฉ๐ฅ๐ ๐จ๐ ๐ญ๐ก๐ข๐ฌ ๐๐ซ๐๐ฆ๐ข๐ฎ๐ฆ ๐๐๐ฉ๐จ๐ซ๐ญ @ https://www.transparencymarketresearch.com/sample/sample.php?flag=S&rep_id=374
Demand for non-invasive prenatal testing (NIPT) is increasing in several countries owing to the rise in number of doctors preferring advanced non-invasive DNA test for high-risk pregnancies, desire to delay pregnancy, and growth in pregnancy-related issues in the second or third trimester. The global market (NIPT) market is highly saturated, with the presence of a large number of players.
๐๐จ๐ง-๐ข๐ง๐ฏ๐๐ฌ๐ข๐ฏ๐ ๐๐ซ๐๐ง๐๐ญ๐๐ฅ ๐๐๐ฌ๐ญ๐ข๐ง๐ ๐๐๐ซ๐ค๐๐ญ ๐๐ง๐ญ๐ซ๐จ๐๐ฎ๐๐ญ๐ข๐จ๐ง
Non-invasive prenatal testing (NIPT) is a novel genetic screening method based on the analysis of cell-free fetal DNA in the maternal plasma. NIPT screens for trisomy 21 (Down syndrome) as well as two other less common chromosome abnormalities: trisomy 13 and trisomy 18. Several companies are striving to create advanced screening methods that are sensitive and accurate in the early diagnosis of genetic abnormalities in infants.
Next-generation sequencing (NGS) is a commonly used technology for the identification of trisomy, micro-deletions, and aneuploidies in chromosomes. NGS-based noninvasive prenatal tests are different from other techniques, as they can be performed as early as 10 weeks of pregnancy. Additionally, other noninvasive prenatal tests offer about 96% accuracy, while NGS-based tests are more than 99% accurate.
๐๐ง๐ช๐ฎ๐ข๐ซ๐ ๐๐๐๐จ๐ซ๐ ๐๐ฎ๐ฒ๐ข๐ง๐ ๐ญ๐ก๐ ๐ซ๐๐ฌ๐๐๐ซ๐๐ก ๐ซ๐๐ฉ๐จ๐ซ๐ญ ๐๐จ๐ซ ๐ฏ๐ข๐ญ๐๐ฅ ๐ฎ๐ง๐๐๐ซ๐ฌ๐ญ๐๐ง๐๐ข๐ง๐ ๐ฌ- https://www.transparencymarketresearch.com/sample/sample.php?flag=EB&rep_id=374
๐๐๐ฑ๐ญ-๐ ๐๐ง๐๐ซ๐๐ญ๐ข๐จ๐ง ๐ฌ๐๐ช๐ฎ๐๐ง๐๐ข๐ง๐ (๐๐๐) ๐ฌ๐ฒ๐ฌ๐ญ๐๐ฆ๐ฌ ๐ฅ๐๐๐ ๐ญ๐ก๐ ๐ ๐ฅ๐จ๐๐๐ฅ ๐๐จ๐ง-๐ข๐ง๐ฏ๐๐ฌ๐ข๐ฏ๐ ๐๐ซ๐๐ง๐๐ญ๐๐ฅ ๐๐๐ฌ๐ญ๐ข๐ง๐ (๐๐๐๐) ๐ฆ๐๐ซ๐ค๐๐ญ-
NGS systems provide precise and accurate detection of fetal chromosomal abnormalities by sequencing large amounts of DNA.
They are scalable to meet the increasing demand for NIPT, and their cost-effectiveness makes them preferable to other methods. NGS systems are widely available, improving access for pregnant women. Furthermore, NGS technology enables the development of new NIPT tests that detect a broader range of abnormalities, driving market growth.
In comparison to other techniques like NGS systems, ELISA kits are a generally accessible and affordable choice for NIPT. They are useful for point-of-care testing and smaller laboratories since they are comparatively simple. Trisomy 21 and trisomy 18 are two frequent fetal chromosomal disorders that ELISA tests are highly accurate at identifying. A greater spectrum of abnormalities is detected by ELISA-based NIPT tests, fostering continued market expansion.
๐๐จ๐ฐ ๐๐ซ๐ ๐๐๐ฒ ๐๐ฅ๐๐ฒ๐๐ซ๐ฌ ๐๐๐ฏ๐จ๐ฅ๐ฎ๐ญ๐ข๐จ๐ง๐ข๐ณ๐ข๐ง๐ ๐ญ๐ก๐ ๐๐ง๐๐ฎ๐ฌ๐ญ๐ซ๐ฒ?
The Non-invasive Prenatal Testing industry is highly competitive, with several players operating globally. The market is characterized by the presence of both established as well as emerging players. The key players in the market are engaged in strategic partnerships, collaborations, and mergers and acquisitions to expand their market presence.
โข Berry Genetics
โข BGI
โข Laboratory Corporation of America Holdings
โข Agilent Technologies, Inc.
โข Illumina, Inc.
โข F. Hoffmann-La Roche Ltd.
โข Natera, Inc.
โข PerkinElmer Inc.
โข Eurofins LifeCodexx AG
โข IGENOMIX
โข Pacific Biosciences
๐๐๐ฏ๐ ๐๐ง๐ฒ ๐๐ฎ๐๐ซ๐ฒ? ๐๐ฌ๐ค ๐๐ฎ๐ซ ๐๐ฑ๐ฉ๐๐ซ๐ญ๐ฌ: https://www.transparencymarketresearch.com/sample/sample.php?flag=ASK&rep_id=374
๐๐๐ฒ ๐๐๐ ๐ฆ๐๐ง๐ญ๐ฌ ๐จ๐ ๐ญ๐ก๐ ๐๐จ๐ง-๐ข๐ง๐ฏ๐๐ฌ๐ข๐ฏ๐ ๐๐ซ๐๐ง๐๐ญ๐๐ฅ ๐๐๐ฌ๐ญ๐ข๐ง๐ ๐๐๐ซ๐ค๐๐ญ
๐๐๐ฌ๐ญ ๐๐ฒ๐ฉ๐
โข Materni21
โข Harmony
โข Panorama
โข Verifi
โข NIFTY
โข Others
๐๐ฉ๐ฉ๐ฅ๐ข๐๐๐ญ๐ข๐จ๐ง
โข Trisomy
โข Micro-deletions Symptoms
โข Others (including sex chromosomes disorders)
๐๐๐๐ก๐ง๐จ๐ฅ๐จ๐ ๐ฒ
โข NGS
โข WGS
โข Others
๐๐ง๐-๐ฎ๐ฌ๐๐ซ
โข Hospitals
โข Diagnostic Laboratories
โข Others
๐๐๐ฒ ๐๐๐ฏ๐๐ฅ๐จ๐ฉ๐ฆ๐๐ง๐ญ๐ฌ ๐ข๐ง ๐๐ฅ๐จ๐๐๐ฅ ๐๐จ๐ง-๐ข๐ง๐ฏ๐๐ฌ๐ข๐ฏ๐ ๐๐ซ๐๐ง๐๐ญ๐๐ฅ ๐๐๐ฌ๐ญ๐ข๐ง๐ ๐๐๐ซ๐ค๐๐ญ
โข ๐๐ง ๐๐๐ง๐ฎ๐๐ซ๐ฒ ๐๐๐๐, QIAGEN collaborated with Atila BioSystems to supply non-invasive prenatal testing (NIPT) solutions to QIAGEN’s dPCR business
โข ๐๐ง ๐๐ฎ๐ฅ๐ฒ ๐๐๐๐, Pacific Biosciences signed a definitive merger agreement to acquire Omniome, a San Diego-based company developing a highly differentiated, proprietary short-read sequencing platform capable of delivering high accuracy. The company chose Omniome due to its novel approach to getting a precise short-read sequencing platform to fast-growing clinical application areas in oncology, transcriptomics, metagenomics, and non-invasive prenatal testing (NIPT).
โข ๐๐ง ๐๐๐๐, ๐๐๐ญ๐๐ซ๐, ๐๐ง๐. launched Vistara, a NIPT solution that screens single gene abnormalities across 30 genes. It is an alternative/complement to Panorama and screens for severe skeletal, cardiac, and oncological conditions that are related to cognitive disorders and require surgical interventions.
๐๐ซ๐จ๐ฐ๐ฌ๐ ๐๐จ๐ซ๐ ๐๐๐ฅ๐๐ญ๐๐ ๐๐๐ฉ๐จ๐ซ๐ญ๐ฌ ๐๐ฒ ๐๐ซ๐๐ง๐ฌ๐ฉ๐๐ซ๐๐ง๐๐ฒ ๐๐๐ซ๐ค๐๐ญ ๐๐๐ฌ๐๐๐ซ๐๐ก-
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Nikhil Sawlani
Transparency Market Research Inc.
+ +1 518-618-1030
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