Unlocking BioCompute Objects: Velsera's Commitment to Interoperability and Regulatory Excellence. At Velsera, we're shaping the future of bioinformatics and regulatory excellence. Collaborating with the BioCompute Object (BCO) community, we've pioneered the BCO standard to communicate complex Next Generation Sequencing (NGS) workflows for regulatory review. Our award-winning app simplifies the process of generating BCOs and won first prize in the precisionFDA BioCompute Object App-a-thon. The challenge? Demonstrating BCOs' interoperability. The introduction of Neoantigen Workflows is a prime example of our leadership on this journey. Our BCO app effortlessly generates a BCO from this sophisticated workflow, highlighting regulatory submission best practices. We're proud to partner with the Biocompute Object Working Group to set a standard for excellence, showing BCOs can seamlessly operate within the FDA. The Velsera team is excited to participate in the FDA Computing Days, Sept. 12-13, 2023! Our BCO working group, proudly sponsored by the FDA, is part of the innovation competition. Embrace innovation, interoperability, and regulatory excellence with Velsera. Interested in our BCO work? Reach out to our team today! https://lnkd.in/gdkw4vDa #EraofVelsera #BCOInteroperability #Bioinformatics #RegulatoryExcellence #PrecisionFDA #NeoantigenWorkflow https://lnkd.in/gbGXj6YU
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What an incredible few quick days in Basel at BioTechX Europe 2024! 🙌 The Velsera team had an amazing time connecting with innovators and leaders at #BioTechX EU. From insightful conversations at booth 1038 to captivating talks by Jack DiGiovanna and Tatjana Kovacevic, PhD, we showcased how we’re pushing the boundaries of genomics and bioinformatics. A huge thank you to everyone who stopped by. Let’s continue driving innovation and transforming research into reality! For those who couldn’t join, but are curious, connect with us here: https://lnkd.in/gRTjwsJj #EraofVelsera #DrugDiscovery #PrecisionMedicine #Tradeshow #Bioinformatics
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Save Time with an Enhanced NGS Workflow Our Clinical Genomics Workspace (CGW) offers features tailored to streamline your somatic tertiary analysis and reporting workflow. 🔸 Save time by retaining previous biomarker reporting decisions 🔸 Boost reporting efficiency with templated interpretation text based on the content you choose to report 🔸 Stay up-to-date with highlighted updates to clinical evidence 🔸 Streamline your lab’s clinical reporting of comprehensive molecular result CGW serves as a comprehensive analysis and reporting solution for clinical NGS data, leveraging an industry-leading knowledgebase, robust clinical reporting, and customized laboratory services. Let’s work together to enhance your workflow. Learn more: https://lnkd.in/gs59SbTf #PrecisionMedicine #NGS #EraOfVelsera
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It’s Day 2 at BioTechX EU! Stop by booth 1038 today for some refreshing flavored water and pastries, in addition to chatting with the Velsera team. 🍋 Plus, don’t miss Tatjana Kovacevic, PhD talk at 15:30 pm on “Leveraging Machine Learning and AI for Bioinformatics on the Seven Bridges Platform”. Come hydrate, connect, and learn how we can power your discoveries! 💡 #Bioinformatics #Innovation #EraofVelsera #DrugDiscovery #PrecisionMedicine #Tradeshow
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Don’t let FOMO hold you back! If you missed our latest Velsera in Action webinar by Sarah Clancey Overton, there’s still time to catch up. Here’s what you missed: 🔸New GSP codes 🔸The latest trends in NGS reimbursement 🔸2024 CPT code updates set to transform your RCM strategy 🔸Expert tips to boost your revenue with Velsera Take your RCM strategy to the next level! Watch the on-demand recording now https://lnkd.in/g9TpKgJA #RCM #CPTCodes2024 #NGSReimbursement #GSPcodes #EraofVelsera
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Halfway through the day at BioTechX EU 2024 in Basel — have you stopped by to meet us yet? Visit booth 1038 to learn more about how Velsera is transforming research with data insights and solutions, and be sure to grab some of the remaining pastries from round two before they’re gone! #EraofVelsera #DrugDiscovery #PrecisionMedicine #Tradeshow
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Struggling with inefficiencies in your genomic workflows? Don’t let outdated references hold you back! Velsera is live at BioTechX Europe! Come visit us at Booth 1038 for insights on how to streamline your processes, reduce errors, and gain more accurate results - plus, grab some pastries while you’re there! Join our Chief Science Officer, Jack DiGiovanna, at 15:30 pm for his talk on “Improving Accuracy and Efficiency Leveraging a Human Pangenome Reference”. Can’t make the show? No worries! Discover our solutions here: https://lnkd.in/gP-Czn7A #EraofVelsera #Genomics #Innovation #Tradeshow #DrugDiscovery
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Breaking Barriers in Precision Medicine for Spain & Portugal. We understand the growing pressure on clinical labs to deliver accurate, timely genomic insights, while facing challenges like complex workflows and limited regional support. That’s why we’re thrilled to announce our strategic partnership with Diagnóstica Longwood. Together, we’re delivering a complete, end-to-end solution that simplifies genetic data analysis for oncology & inherited diseases. Faster, more accurate results mean better patient care—driving precision medicine forward across the Iberian market. Read the full announcement here: https://lnkd.in/g3qwigeU #PrecisionMedicine #NGS #EraOfVelsera
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🚀 Mark your calendars! On October 24th at 11 am EST, we’re exploring the future of genomic research with our webinar, Improving Accuracy and Efficiency Leveraging a Human Pangenome Reference. In this webinar, we’ll explore how the Human Pangenome Reference is transforming bioinformatics, driving precision, and streamlining workflows for researchers worldwide. Whether you’re looking to enhance the accuracy of your data or boost your research efficiency, this webinar is a must-attend! What you’ll learn: 🔸 Enhanced Genomic Accuracy: See how pangenome references improve equity, scientific rigor, and clinical utility over standard methods. 🔸 Superior Alignment: Learn how better sequencing read alignment leads to more accurate variant calling, particularly in complex regions like MHC. 🔸 Efficiency Gains: Understand how these technologies cut computational costs and time, removing the need for expensive joint calling. Register today for one of our limited spots here: https://lnkd.in/gVePZk-j #EraofVelsera #DrugDiscovery #PrecisionMedicine #Bioinformatics
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Less than a week away from an event you won’t want to miss in Basel, BioTechX EU 2024! We’re excited to have two of Velsera’s experts sharing their knowledge: 🔸 Jack DiGiovanna, Chief Science Officer - Oct 9th at 15:30 PM, Topic: Improving Accuracy and Efficiency Leveraging a Human Pangenome Reference 🔸 Tatjana Kovacevic, PhD, Solution Scientist - Oct 10th at 15:30 PM, Topic: Leveraging Machine Learning and AI for Bioinformatics on the Seven Bridges Platform Can’t attend the sessions, but will be at the show? Stop by booth 1038 to meet Jack, Tatjana, and other Velsera experts to help solve your bioinformatics challenges while indulging in pastries and flavored water. We look forward to seeing you in Basel VERY soon! Click here to connect with us ahead of the show: https://lnkd.in/gb22GEg5 #DrugDiscovery #EraofVelsera #Tradeshow #PrecisionMedicine
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Just in! The 2025 CLFS & Gapfill files dropped last Thursday, and we've got the latest insights on the new GSP codes! Whether you're ready for the 2024 CPT code updates or just getting started, our newest webinar in the Velsera in Action Series, Optimizing RCM with 2024 CPT Code Updates has you covered! Join us tomorrow October 3rd at 8 AM PST for a fast-paced 20 minutes where we’ll break down the latest NGS reimbursement trends, explain how the new codes will impact your RCM, and show you how to boost your revenue with Velsera. Don’t wait—register now and secure your spot! https://lnkd.in/dTdHTUnK #RCM #CPTCodes2024 #NGSReimbursement #EraofVelsera #VelseraInAction
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