Amniocentesis

$12.85+ Bn Non-Invasive Prenatal Testing (NIPT) Markets - Global and Regional Market Analysis, Forecast, and Competition Landscape 2023-2024 & 2033 - ResearchAndMarkets.com

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Giovedì, Maggio 23, 2024
Biotechnology, Genetics, Health, NGS, Insurance, Chromosome, DNA, Trisomy, Region, BGI Group, Amniocentesis, Risk, Maternal death, Diagnosis, Ecosystem, DSM-IV codes, Safety, NIPT, Down syndrome, Blood, Prenatal care, Growth, Research, Incidence, Workflow, Genomics, Nucleic acid thermodynamics, Labcorp, PCR

The NIPT market in the Asia-Pacific region is witnessing significant growth of 15.43% in the forecast period, marked by increasing number of market players, and shifting healthcare landscape.

Key Points: 
  • The NIPT market in the Asia-Pacific region is witnessing significant growth of 15.43% in the forecast period, marked by increasing number of market players, and shifting healthcare landscape.
  • In 2022, Asia-Pacific accounted for a share of 19.50% of the global NIPT market.
  • The global NIPT market is characterized by intense competition, as established entities and emerging players compete for a share of the market.
  • The global NIPT market (by method) was dominated by the cfDNA segment in FY2022.

Global Prenatal Testing Market Report 2024: Historical Revenue Data for 2021-2022, Estimates for 2023, Forecasts for 2024, and CAGR Projections through 2028 - ResearchAndMarkets.com

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Venerdì, Maggio 3, 2024
Baby, Maternity, Health, Consumer, Other Health, Insight, Noninvasive prenatal testing, Pregnancy, DSM-IV codes, Research, Genetic testing, Labcorp, Government, NIPT, Amniocentesis, ESG, Thermo Fisher Scientific, Maternal death, Chromosome, Illumina, Inc., Biomarker

The "Global Prenatal Testing Market 2023-2028" report has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Global Prenatal Testing Market 2023-2028" report has been added to ResearchAndMarkets.com's offering.
  • The scope of the prenatal testing market is extensive and continually evolving, reflecting the dynamic landscape of technologies and methodologies employed to assess fetal health during pregnancy.
  • This market is characterized by its global reach, with varying levels of adoption and accessibility across different regions.
  • The report covers geographic regions in detail, so companies interested in expanding their geographic reach will also find this helpful study.

BILLIONTOONE MITIGATING RHOGAM(R) SHORTAGE WITH UNITY FETAL RhD™ NON-INVASIVE PRENATAL TEST

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Mercoledì, Aprile 17, 2024
Fetus, FDA, CTA, Blood, RHD (gene), Anemia, Pregnancy, Wellstar Health System, Health care, HDFN, Placenta, Parent, Scientific Reports, Patient, Amniocentesis, Physician, Immune system, Antibody, Janssen Pharmaceuticals, Plasma, Dietary supplement

MENLO PARK, Calif., April 17, 2024 /PRNewswire/ -- BillionToOne, a molecular diagnostics company with a mission to create powerful and accurate tests that are accessible to all, has reached a milestone of testing over 80,000 patients for Rh incompatibility, which develops when a pregnant patient has Rh-negative blood and the baby has Rh-positive blood. In rare cases this incompatibility can lead to a serious issue in which the pregnant patient's immune system will attack their baby's red blood cells as foreign.

Key Points: 
  • However, the FDA recently announced that the most common brand of this medication, RhoGAM(R), is in shortage .
  • Utilizing cell-free DNA in maternal plasma, the UNITY Fetal RhD Non-Invasive Prenatal Test can determine fetal RhD status," said Jennifer Hoskovec, MS, Certified Genetic Counselor and Senior Director of Medical Affairs at BillionToOne.
  • The UNITY Fetal RhD NIPT offers a reliable and convenient alternative to traditional methods of determining fetal RhD status, such as paternal testing and invasive procedures like amniocentesis.
  • The UNITY Fetal RhD NIPT accurately determines the RhD status of the fetus from maternal blood as early as 10 weeks gestation.

Global and Regional Rare Disease Genetic Testing Market Analysis & Forecasts Report 2023-2033 - ResearchAndMarkets.com

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Lunedì, Ottobre 9, 2023
Health, Genetics, Diagnosis, Incidence, Parent, Hospital, DSM-IV codes, Physician, Exome, Plasma, Research, SRL Diagnostics, Genome, Prevalence, PCR, BGI Group, NGS, DNA, CVS, Risk, SNV calling from NGS data, Sanger, Massive parallel sequencing, Metabolism, Amniocentesis, Genetic code, Disease, State Key Laboratories, R, Inherit, Genomics, Patient, Polymerase chain reaction, WES, WGS, Genetic counseling, Growth, Genetic testing, Region, National Centre for Foreign Animal Disease, Gene, Rare, Chromosome, Fetus, Cardiogenic shock, Serum, Birth, Gastroenterology, Pharmaceutical industry, Medical imaging, Vaccine, Medical device, Dietary supplement

The "Rare Disease Genetic Testing Market - A Global and Regional Analysis: Focus on Disease Type, Offering, Specialty Type, Sample Type, Trait Type, Technology, Age Group, End User, and Country Analysis - Analysis and Forecast, 2023-2033" report has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Rare Disease Genetic Testing Market - A Global and Regional Analysis: Focus on Disease Type, Offering, Specialty Type, Sample Type, Trait Type, Technology, Age Group, End User, and Country Analysis - Analysis and Forecast, 2023-2033" report has been added to ResearchAndMarkets.com's offering.
  • The global market for rare disease genetic testing encompasses an array of panels and tests that excel in detecting rare diseases.
  • The global rare disease genetic testing market has experienced remarkable growth, driven by the escalating demand for early detection of rare diseases.
  • Moreover, a maximum number of rare disease testing is done there, due to which these regions hold the maximum share in the global rare disease genetic testing market.

Global and Regional Rare Disease Genetic Testing Market Report 2023-2033: Early Detection Demand and Innovative Systems Usher in New Era for Rare Disease Genetic Testing

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Martedì, Ottobre 3, 2023
Chromosome, DNA, Sanger, National Centre for Foreign Animal Disease, Gastroenterology, Prevalence, BGI Group, DSM-IV codes, Serum, Disease, Fetus, Genomics, Parent, Hospital, Cardiogenic shock, SRL Diagnostics, NGS, Amniocentesis, CVS, Genetic testing, Research, Birth, Genetic code, Exome, Incidence, Genetic counseling, Plasma, Metabolism, Patient, Polymerase chain reaction, Physician, Risk, State Key Laboratories, WGS, Inherit, Growth, Diagnosis, Region, R, Rare, WES, SNV calling from NGS data, Massive parallel sequencing, Gene, PCR, Genome, Pharmaceutical industry, Medical imaging, Vaccine, Medical device, Dietary supplement

The global market for rare disease genetic testing encompasses an array of panels and tests that excel in detecting rare diseases.

Key Points: 
  • The global market for rare disease genetic testing encompasses an array of panels and tests that excel in detecting rare diseases.
  • Among the most prevalent rare disease genetic testing panels are those tailored for gastroenterology, endocrine and metabolic disorders, and neurological diseases.
  • The global rare disease genetic testing market has experienced remarkable growth, driven by the escalating demand for early detection of rare diseases.
  • Moreover, a maximum number of rare disease testing is done there, due to which these regions hold the maximum share in the global rare disease genetic testing market.

Noninvasive Prenatal Testing: The Luna Prenatal Test for Isolation of Circulating Fetal Cells Early in Pregnancy, Upcoming Webinar Hosted by Xtalks

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Lunedì, Marzo 6, 2023
CVS, Walker–Warburg syndrome, Health, Blood, Cell, Pregnancy, Research, Fetus, Confined placental mosaicism, Luna, Trisomy, Amniocentesis, Risk, DSM-IV codes, Knowledge, R, Noninvasive prenatal testing, POMT1, Genetics, Dietary supplement, Genetic distance, Syndactyly-nystagmus syndrome due to 2q31.1 microduplication

TORONTO, March 6, 2023 /PRNewswire-PRWeb/ -- For decades, many groups around the world have pursued the isolation and genetic analysis of circulating fetal cells from maternal peripheral blood as an improved form of noninvasive prenatal testing. However, the exceeding rarity of these cells in the blood of pregnant women has proven a challenging obstacle in the establishment of a reliable test methodology.

Key Points: 
  • In this free webinar, learn about a breakthrough in the reliable isolation and successful analysis of circulating fetal cells for noninvasive prenatal testing early in pregnancy.
  • The featured speaker will discuss how the Luna Prenatal Test isolates and analyzes single circulating fetal cells early in pregnancy.
  • Attendees will learn how the Luna Prenatal Test makes a positive difference in patient care and reproductive health.
  • In collaboration with Juno Genetics, the Luna Prenatal Test isolated circulating fetal cells from a pregnancy at risk of Walker-Warburg Syndrome.

OGM Evaluated as a Method for Investigating Abnormal NIPT Results due to its Ability to Detect Chromosomal Structural Variations Found in Recurrent Pregnancy Loss

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Venerdì, Ottobre 14, 2022
Adoption, Non-functional testing, Genetic counseling, SAN, U.S. Securities and Exchange Commission, OGM, KT, Autism, Risk, Medicine, NIPT, Annual report, CMA, Patient, Lineagen, Biology, Hospital Insurance and Diagnostic Services Act, Research, Security (finance), Nasdaq, Private Securities Litigation Reform Act, Software, Amniocentesis, Company, Doctor of Philosophy, Karyotype, Chromosomal rearrangement, CCR, Genomics, Pregnancy loss, GLOBE, Infertility, Genome, Forward-looking statement, Chromosome, Pregnancy, COVID-19, Solution, Medical imaging

The study sought to determine OGMs utility for detection of chromosome breakages and fusions found in complex chromosomal rearrangements (CCR), which can significantly increase an abnormal pregnancy outcome for carrier couples.

Key Points: 
  • The study sought to determine OGMs utility for detection of chromosome breakages and fusions found in complex chromosomal rearrangements (CCR), which can significantly increase an abnormal pregnancy outcome for carrier couples.
  • The researchers used OGM as part of a confirmatory workflow after amniocentesis, karyotyping (KT), and chromosomal microarray analysis (CMA) identified suspected structural rearrangements with unknown origins, believed to indicate a CCR event.
  • We believe OGM could be used as a comprehensive follow-up genome analysis in cases with a positive NIPT screen or for some high-risk pregnancies.
  • The Companys mission is to transform the way the world sees the genome through OGM solutions, diagnostic services and software.

Global Non Invasive Prenatal Testing Market Report (2022 to 2030) - Asia-Pacific is Expected to Exhibit the Highest CAGR Over the Forecast Period - ResearchAndMarkets.com

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Giovedì, Ottobre 6, 2022
Biotechnology, Genetics, Health, Adoption, Lists of diseases, Hospital, Risk, Technology, Government, Growth, Infection, NIPT, CAGR, List of mammalian gestation durations, Patient, Whole genome sequencing, Investment, Amniocentesis, Chromosome, Application, COVID-19, Down syndrome, Incidence, Down, DNA, Prenatal care, USD, Method, Health insurance, Pharmaceutical industry

The global non invasive prenatal testing market size is expected to reach USD 7.71 billion by 2030, according to this report., expanding at a CAGR of 9.61% from 2022 to 2030.

Key Points: 
  • The global non invasive prenatal testing market size is expected to reach USD 7.71 billion by 2030, according to this report., expanding at a CAGR of 9.61% from 2022 to 2030.
  • The increasing incidence of chromosomal abnormalities is expected to accelerate market growth.
  • Of all the countries, there is a substantial opportunity in China for non invasive prenatal screening, with nearly 14.65 million annual births and increasing number of high-risk pregnancies.
  • Cell-free DNA is increasingly being utilized in predicting the risk of genetic disorders in prenatal care via various genetic analyses
    Asia Pacific is expected to exhibit the highest CAGR over the forecast period.

DGAP-News: Biotest AG: Biotest grants Renate & Hans Schleussner Research Award for the first time

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Lunedì, Luglio 25, 2022
Infection, University, III, Awareness, Woman, Observational study, Research, Immunoglobulin A, Institute, Safety, Fetus, Obstetrics, Immunoglobulin M, Immunoglobulin G, Pregnancy, Lists of diseases, Cytomegalovirus, CMV, Huber loss, Patient, National Institute of Virology, Amniocentesis, Child, Immunodeficiency with hyperimmunoglobulin M, Pharmaceutical industry, Birth control, Vaccine, Virology

Biotest is currently also conducting a phase III clinical trial with CMV hyperimmunoglobulin in pregnant women.

Key Points: 
  • Biotest is currently also conducting a phase III clinical trial with CMV hyperimmunoglobulin in pregnant women.
  • Dr.PhilippKolb from the Institute of Virology at the University of Freiburg is the first winner of the Renate&HansSchleussner Research Award.
  • The award supports a research project of the excellent winner in the field of cytomegalovirus (CMV) infection.
  • The ordinary and preference shares of Biotest AG are listed in the Prime Standard on the German stock exchange.

Premier Medical Laboratory Services Now Offering Noninvasive Prenatal Testing

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Mercoledì, Maggio 18, 2022
Cancer, Diabetes, Risk, DNA, NGS, Blood, Sex, COLA, Toxicology, Degenerative disease, Amniocentesis, CVS, Placenta, Edwards syndrome, Doctor of Philosophy, Multimedia, Patient, Woman, Down syndrome, Amniotic fluid, Insurance, Health, Edwards, Greenville Triumph SC, Method, Research, Whole genome sequencing, Industry, Aneuploidy, NIPT, Nucleic acid thermodynamics, 2020 Greenville Triumph SC season, Chromosome, Pregnancy, Chorionic villus sampling, CLIA, Trisomy, CEO, Medical imaging

GREENVILLE, S.C., May 18, 2022 /PRNewswire/ -- Premier Medical Laboratory Services (PMLS) is announcing today that they have added Noninvasive Prenatal Testing (NIPT) to their full line of medical diagnostic testing and risk screening services.

Key Points: 
  • GREENVILLE, S.C., May 18, 2022 /PRNewswire/ -- Premier Medical Laboratory Services (PMLS) is announcing today that they have added Noninvasive Prenatal Testing (NIPT) to their full line of medical diagnostic testing and risk screening services.
  • As a laboratory, PMLS strives to offer only the most advanced and accurate testing and screening available for optimal patient care.
  • Premier Medical Laboratory Services (PMLS), headquartered in Greenville, South Carolina, is the official health and wellness partner of the Greenville Triumph and an advanced molecular diagnostics lab fully certified by top laboratory accrediting organizations, including CLIA and COLA.
  • Their expansive menuof highly advanced tests and screenings include genomic risk assessment assays for various cancers, heart disease, and diabetes, as well as women's health panels, toxicology, allergy testing, pharmacogenomics, routine blood chemistry, and noninvasive prenatal testing (NIPT).