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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🔬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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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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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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Can the presence of specific genetic alterations and MRD status help predict outcomes for adult patients with KMT2A-rearranged B-cell precursor ALL? A recent GRAALL study by Kim et al. explores this question. Check out our publication summary here to find out more: https://loom.ly/66-THPU #ALLsm #leusm
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Watch this 1-hour video module on starting a dialogue with patients about genetic screening and NIPT. Learn to reassure and educate patients, establishing a patient-centred model of care. https://bit.ly/3MVWVjM #cpd #cpdtraining #CME #meded #gp
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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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Some patients feel isolated or alone because of an undiagnosed condition. With genetic testing results they get the chance to connect with others who are going through a similar situation. To learn more, read our blog here: https://ow.ly/Jxw550PnPu0
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The video for this programme is made with easy-to-follow schematics for simplified learning. It covers how & when to use PARP inhibitors. Expert Neal Shore considers the best PARPi monotherapy treatment choice based on genetic test results. 👀https://ow.ly/NMSV50Px0fz #MedEd
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Are you testing for Hereditary Hemochromatosis (HH) in your lab? To diagnose or rule out hereditary hemochromatosis, persons with abnormal serum iron markers and unexplained liver or heart disease, for example, should undergo genetic testing. We are offering two distinct test systems for the diagnosis of HH - fast and reliable. You have the option between two different technologies to provide your individual result. 🧬 FluoroType® HH C282Y VER 1.0 and FluoroType® HH H63D VER 1.0 rely on the innovative FluoroType® technology. 🧬 GenoType HH VER 2.0 utilizes the reliable DNA•STRIP technology Which one would you choose for your individual testing needs? Get informed now! #BrukerMID #humangenetics #moleculardiagnostics
World HH Week | Discover our portfolio!
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