📣 Webinar reminder! Vi ricordiamo il webinar di oggi di SOPHiA GENETICS dal vivo presso Frontline Genomics "Enhancing variant interpretation: Obtaining answers from a vast universe of data"! 📅 ⏰ Mercoledì 17 luglio, 15:00 (ora di Roma) 🗣️ Prenotate ora la vostra partecipazione! https://loom.ly/vAyOX9g
📣 ONE DAY LEFT! Don't miss our live webinar at Frontline Genomics "Enhancing variant interpretation: Obtaining answers from a vast universe of data" 🧬 💡Join us for a webinar where we tackle the challenges of pinpointing pathogenic mutations from large, complex datasets. In this webinar, we will demonstrate how variant interpretation with Alamut™ Visual Plus can improve the accuracy and speed of variant interpretation, using specific case studies, such as detecting compound heterozygous variants in Charcot-Marie-Tooth Disease, and Alu insertions in breast cancer. Rolph Pfundt, Clinical Molecular Geneticist at Radboud University Medical Centre in the Netherlands, will share insights into his variant interpretation workflow, highlighting how Alamut™ Visual Plus enables the identification of complex variants with greater ease and precision. Join this insightful exchange and learn how integrating Alamut™ Visual Plus into your NGS workflow can streamline your genomic analysis, making it quicker and easier. ➡️ Book your spot here: https://loom.ly/vAyOX9g Can't attend live? Register today and access the recorded session on-demand at your own convenience!
