Agilent Pharma - Small Molecule and Biologics’ Post

Interested in Optical Genome Mapping and its various uses? Join this Bionano webinar on May 2nd to explore how OGM is used in cell and gene therapy!

Did you know that there is a tool for genetic diagnosis in complex patients? Through the sequencing of the whole genome and its subsequent interpretation, oriented to the clinical signs and symptoms of the patient. In this #TalkingAboutGenetics, 👨⚕️Dr. Jorge Armando Rojas Martinez, a medical geneticist at Veritas, explains it in detail. For more information about #GenomeDx visit ➡️ https://hubs.ly/Q02dZmT-0

In the latest issue of The Journal of Perinatology-Neonatology, Madhuri Hegde, Senior Vice President and Chief Scientific Officer at #Revvity, delves into the cost-effective potential of employing first-line Whole Genome Sequencing to diagnose #genetic conditions in children. The aim? Minimizing delays and expediting prompt treatments. Check out the insightful article on Pages 32-33 Link: http://ms.spr.ly/6042cb9ou

The Tapestri Genome Editing Solution empowers researchers with a high level of sensitivity, specificity, and reproducibility when analyzing knockout and base editing experiments. In this App Note, learn more about how by examining zygosity and the simultaneous occurrence of on- and off target edits, researchers can gain invaluable insights into the depth of editing within individual cells. Get all the details in the App Note here 👉 https://lnkd.in/gebbGcy6 #technicalnote #appnote #genomeediting #geneediting #genetherapy #celltherapy #crispr

At a recent workshop we attended, participants discussed the future of Variants of Uncertain Significance (VUS) and whether they would be obsolete by 2030. The consensus? Most experts disagreed. This underscores the ongoing challenge of VUS in genetic testing and highlights the critical role of tools like MAVEvidence in providing clarity. As VUS remain a significant hurdle in clinical genetics, platforms like MAVEvidence are more important than ever. By offering clear, actionable insights based on comprehensive data, MAVEvidence helps clinicians and researchers tackle genetic uncertainty and make informed decisions—ensuring that advancements in precision medicine continue beyond 2030. #MAVEvidence #GeneticTesting #VUS #PrecisionMedicine #ConstantiamBiosciences #HealthcareInnovation #Genomics

In support of #rarediseaseday, Stephen Kingsmore willing posed with me in my zebra stripes at Rady Children's Institute for Genomic Medicine! Every single day Dr. Kingsmore and all my other colleagues work to make ultra-rapid whole genome sequencing testing available for every patient who might benefit. For us, it's our mission to try to take some of the burden off the moms and dads of those little kiddos who tenaciously strive to find answers and get help for their kids. I can't imagine what they go through. #raredisease #rarediseaseday #wholegenomesequencing #genetictesting #geneticdisease

Calling all healthcare professionals! Let @Franklin streamline your genetic sequencing journey. With experts and a growing community, finding the right lab is easier than ever. Ready to step up your game? Click here to learn more. #sequencing #genechat #genetics

Say goodbye to re-analysis for undiagnosed cases! With GenomeAlert you will get a monthly update to notify you if a variant in one of your patient samples is re-classified as pathogenic.

In the fast-evolving field of genetic diagnostics, staying updated with the latest variant classifications can mean the difference between a missed opportunity and a life-saving intervention. Our new service SeqOne GenomeAlert! not only fully automates the reevaluation of genetic variants using the latest updates from ClinVar, it also introduces an innovative layer of automated curation and an intuitive interface. This allows biologists to effortlessly navigate through candidates for new & revoked diagnostics, ensuring information is just a click away 🧬. Learn more & see GenomeAlert! in action here 👉 https://lnkd.in/e-h2QTF4 #SeqOneGenomics #GenomicsRevolution #PersonalizedMedicine #HealthTech #NGS

🧬Discover Your Perfect Lab Match!🧬 Let Franklin by Genoox guide you to a trusted sequencing lab partner for your patient's genetic tests. Specify your needs, and we'll pair you with a verified genetic sequencing lab.  Ready to explore?  #sequencing #genechat #genetics