Invitae Generation is our rigorous, evolving approach to clinical genetic testing. Since 2020, we’ve seen a 40% reduction in rates of variants of uncertain significance (VUS) with Invitae Generation technology. Learn more about how to get the answers you need for your patients when you need them: https://invit.ae/3KMoJEG
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📈 Enhance Your Revenue Opportunities 📈 ExtendingME Launching Soon. Partner with Extending ME and offer your patients first-of-its-kind lifetime genetic testing. Not only will you help them live healthier lives, but you’ll also enhance your revenue opportunities. Reach out to learn more! info@extendingme.com #RevenueGrowth #GeneticTesting #HealthcareBusiness
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Unveiling the complexities of genetic testing: A significant 80% of variants in ClinVar are classified as VUS or conflicted. Discover how MAVEvidence by Constantiam Biosciences is pioneering the interpretation of these ambiguous genetic findings, enhancing diagnostic accuracy and advancing patient-centric care. #GeneticTesting #MAVEvidence #HealthTech #PatientCare #vus
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🔬In recognition of May being the Cystic Fibrosis Awareness Month, we would like to bring attention to the efforts behind this genetic disease and how the structural information of CFTR, a key protein in cystic fibrosis research, has brought insights into future drug development research. Read how it was done and how it was recreated utilizing the 3decision software: 👉https://bit.ly/4dJRRd2 #SBDD #cysticfibrosis #3decision #drugdiscovery #Discngine
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How to stay efficient and maintain quality in Cystic Fibrosis genetic testing? 🔬 Dr Andrew Purvis from NHS Scotland explains the impact and success of setting up Devyser CFTR 68 in his laboratory. Read for the full story → https://hubs.ly/Q02q4lK60 #CysticFibrosis #DevyserCFTR68 #NHS
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Are you be interested in learning about the shifting distribution of hemoglobinopathy, and the need for expanded thalassemia genetic testing? Read this insightful blog that recaps how Dr. Robert Akkers and his lab implemented more streamlined thalassemia testing and used real case data to showcase how Devyser’s dedicated software, Amplicon Suite, aids data analysis. Read here: https://bit.ly/3S8vQvf Click the link to discover more about the features in Amplicon Suite ▶️ https://bit.ly/3LoFoyr #NGSTesting #LabInnovation #thalassemia #ngs #genetictesting
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Medical necessity in genetic testing is crucial for effective treatment, optimal resource utilization, and accurate diagnoses. Read our article for detailed insight and its important on this topic. #MedicalNecessity #GeneticTesting #HealthcareOptimization #PatientCare #InsuranceCoverage #Acrev https://www.rfr.bz/llju2fc
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🔬 Exploring Hemoglobinopathy and Thalassemia Testing Are you curious about the evolving landscape of hemoglobinopathy? 🩸 Dr. Robert Akkers delves into this topic, shedding light on the shifting distribution of hemoglobinopathies and the critical need for expanded thalassemia genetic testing. 🧬 In a recent blog, Dr. Akkers shares how his lab streamlined thalassemia testing, leveraging real case data. The star of the show? Devyser’s dedicated software, Amplicon Suite, which enhances data analysis. 🌟
Are you be interested in learning about the shifting distribution of hemoglobinopathy, and the need for expanded thalassemia genetic testing? Read this insightful blog that recaps how Dr. Robert Akkers and his lab implemented more streamlined thalassemia testing and used real case data to showcase how Devyser’s dedicated software, Amplicon Suite, aids data analysis. Read here: https://bit.ly/3S8vQvf Click the link to discover more about the features in Amplicon Suite ▶️ https://bit.ly/3LoFoyr #NGSTesting #LabInnovation #thalassemia #ngs #genetictesting
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Medical necessity in genetic testing is crucial for effective treatment, optimal resource utilization, and accurate diagnoses. Read our article for detailed insight and its important on this topic. #MedicalNecessity #GeneticTesting #HealthcareOptimization #PatientCare #InsuranceCoverage #Acrev https://www.rfr.bz/llju2fc
The Medical Necessity for Genetic Testing in Modern Healthcare | Acrev Solutions
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Professor of Clinical Neurology at University College London, Honorary Consultant Neurologist Director of UCL Huntington’s Disease Centre, Joint Head of Department of Neurodegenerative Disease
Just out from my lab on Biorxiv: Therapeutic validation of MMR-associated genetic modifiers in a human ex vivo model of Huntington’s disease. https://lnkd.in/enTVrVm5
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Our familial studies testing can help families clarify a genetic diagnosis. It can also be useful for segregation analysis for a familial variant for diagnostic or predictive testing. Learn more. https://bit.ly/3WLjY3M
Familial studies - Insights
news.mayocliniclabs.com
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