By 2031, Non-invasive Prenatal Testing Market Expected to Secure US$ 8.4 Billion, with a Notable 14.8 % CAGR| TMR

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Non-invasive Prenatal Testing

High incidence rate of Downโ€™s syndrome are the prominent trends that affect market growth.

WILMINGTON, DELAWARE , UNITED STATES, October 18, 2023 /EINPresswire.com/ — The Global โ€œ๐๐จ๐ง-๐ˆ๐ง๐ฏ๐š๐ฌ๐ข๐ฏ๐ž ๐๐ซ๐ž๐ง๐š๐ญ๐š๐ฅ ๐“๐ž๐ฌ๐ญ๐ข๐ง๐  ๐Œ๐š๐ซ๐ค๐ž๐ญโ€ 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.

๐ƒ๐จ๐ฐ๐ง๐ฅ๐จ๐š๐ ๐š ๐‚๐จ๐ฆ๐ฉ๐ซ๐ž๐ก๐ž๐ง๐ฌ๐ข๐ฏ๐ž ๐’๐š๐ฆ๐ฉ๐ฅ๐ž ๐จ๐Ÿ ๐ญ๐ก๐ข๐ฌ ๐๐ซ๐ž๐ฆ๐ข๐ฎ๐ฆ ๐‘๐ž๐ฉ๐จ๐ซ๐ญ @ 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.

๐๐จ๐ง-๐ข๐ง๐ฏ๐š๐ฌ๐ข๐ฏ๐ž ๐๐ซ๐ž๐ง๐š๐ญ๐š๐ฅ ๐“๐ž๐ฌ๐ญ๐ข๐ง๐  ๐Œ๐š๐ซ๐ค๐ž๐ญ ๐ˆ๐ง๐ญ๐ซ๐จ๐๐ฎ๐œ๐ญ๐ข๐จ๐ง

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.

๐„๐ง๐ช๐ฎ๐ข๐ซ๐ž ๐๐ž๐Ÿ๐จ๐ซ๐ž ๐๐ฎ๐ฒ๐ข๐ง๐  ๐ญ๐ก๐ž ๐ซ๐ž๐ฌ๐ž๐š๐ซ๐œ๐ก ๐ซ๐ž๐ฉ๐จ๐ซ๐ญ ๐Ÿ๐จ๐ซ ๐ฏ๐ข๐ญ๐š๐ฅ ๐ฎ๐ง๐๐ž๐ซ๐ฌ๐ญ๐š๐ง๐๐ข๐ง๐ ๐ฌ- https://www.transparencymarketresearch.com/sample/sample.php?flag=EB&rep_id=374

๐๐ž๐ฑ๐ญ-๐ ๐ž๐ง๐ž๐ซ๐š๐ญ๐ข๐จ๐ง ๐ฌ๐ž๐ช๐ฎ๐ž๐ง๐œ๐ข๐ง๐  (๐๐†๐’) ๐ฌ๐ฒ๐ฌ๐ญ๐ž๐ฆ๐ฌ ๐ฅ๐ž๐š๐ ๐ญ๐ก๐ž ๐ ๐ฅ๐จ๐›๐š๐ฅ ๐๐จ๐ง-๐ข๐ง๐ฏ๐š๐ฌ๐ข๐ฏ๐ž ๐๐ซ๐ž๐ง๐š๐ญ๐š๐ฅ ๐“๐ž๐ฌ๐ญ๐ข๐ง๐  (๐๐ˆ๐๐“) ๐ฆ๐š๐ซ๐ค๐ž๐ญ-

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.

๐‡๐จ๐ฐ ๐š๐ซ๐ž ๐Š๐ž๐ฒ ๐๐ฅ๐š๐ฒ๐ž๐ซ๐ฌ ๐‘๐ž๐ฏ๐จ๐ฅ๐ฎ๐ญ๐ข๐จ๐ง๐ข๐ณ๐ข๐ง๐  ๐ญ๐ก๐ž ๐ˆ๐ง๐๐ฎ๐ฌ๐ญ๐ซ๐ฒ?

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.

โ€ข Berry Genetics

โ€ข BGI

โ€ข Laboratory Corporation of America Holdings

โ€ข Agilent Technologies, Inc.

โ€ข Illumina, Inc.

โ€ข F. Hoffmann-La Roche Ltd.

โ€ข Natera, Inc.

โ€ข PerkinElmer Inc.

โ€ข Eurofins LifeCodexx AG

โ€ข IGENOMIX

โ€ข Pacific Biosciences

๐‡๐š๐ฏ๐ž ๐€๐ง๐ฒ ๐๐ฎ๐ž๐ซ๐ฒ? ๐€๐ฌ๐ค ๐Ž๐ฎ๐ซ ๐„๐ฑ๐ฉ๐ž๐ซ๐ญ๐ฌ: https://www.transparencymarketresearch.com/sample/sample.php?flag=ASK&rep_id=374

๐Š๐ž๐ฒ ๐’๐ž๐ ๐ฆ๐ž๐ง๐ญ๐ฌ ๐จ๐Ÿ ๐ญ๐ก๐ž ๐๐จ๐ง-๐ข๐ง๐ฏ๐š๐ฌ๐ข๐ฏ๐ž ๐๐ซ๐ž๐ง๐š๐ญ๐š๐ฅ ๐“๐ž๐ฌ๐ญ๐ข๐ง๐  ๐Œ๐š๐ซ๐ค๐ž๐ญ

๐“๐ž๐ฌ๐ญ ๐“๐ฒ๐ฉ๐ž

โ€ข Materni21

โ€ข Harmony

โ€ข Panorama

โ€ข Verifi

โ€ข NIFTY

โ€ข Others

๐€๐ฉ๐ฉ๐ฅ๐ข๐œ๐š๐ญ๐ข๐จ๐ง

โ€ข Trisomy

โ€ข Micro-deletions Symptoms

โ€ข Others (including sex chromosomes disorders)

๐“๐ž๐œ๐ก๐ง๐จ๐ฅ๐จ๐ ๐ฒ

โ€ข NGS

โ€ข WGS

โ€ข Others

๐„๐ง๐-๐ฎ๐ฌ๐ž๐ซ

โ€ข Hospitals

โ€ข Diagnostic Laboratories

โ€ข Others

๐Š๐ž๐ฒ ๐ƒ๐ž๐ฏ๐ž๐ฅ๐จ๐ฉ๐ฆ๐ž๐ง๐ญ๐ฌ ๐ข๐ง ๐†๐ฅ๐จ๐›๐š๐ฅ ๐๐จ๐ง-๐ข๐ง๐ฏ๐š๐ฌ๐ข๐ฏ๐ž ๐๐ซ๐ž๐ง๐š๐ญ๐š๐ฅ ๐“๐ž๐ฌ๐ญ๐ข๐ง๐  ๐Œ๐š๐ซ๐ค๐ž๐ญ

โ€ข ๐ˆ๐ง ๐‰๐š๐ง๐ฎ๐š๐ซ๐ฒ ๐Ÿ๐ŸŽ๐Ÿ๐Ÿ, QIAGEN collaborated with Atila BioSystems to supply non-invasive prenatal testing (NIPT) solutions to QIAGEN’s dPCR business

โ€ข ๐ˆ๐ง ๐‰๐ฎ๐ฅ๐ฒ ๐Ÿ๐ŸŽ๐Ÿ๐Ÿ, 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).

โ€ข ๐ˆ๐ง ๐Ÿ๐ŸŽ๐Ÿ๐Ÿ•, ๐๐š๐ญ๐ž๐ซ๐š, ๐ˆ๐ง๐œ. 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.

๐๐ซ๐จ๐ฐ๐ฌ๐ž ๐Œ๐จ๐ซ๐ž ๐‘๐ž๐ฅ๐š๐ญ๐ž๐ ๐‘๐ž๐ฉ๐จ๐ซ๐ญ๐ฌ ๐›๐ฒ ๐“๐ซ๐š๐ง๐ฌ๐ฉ๐š๐ซ๐ž๐ง๐œ๐ฒ ๐Œ๐š๐ซ๐ค๐ž๐ญ ๐‘๐ž๐ฌ๐ž๐š๐ซ๐œ๐ก-

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Nikhil Sawlani
Transparency Market Research Inc.
+ +1 518-618-1030
[email protected]
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