Golden Helix, Inc.

Final day at ACMG 2025! Come to booth #722, this is your last chance to see our latest innovations and enterprise genomic offerings. We’re wrapping up with another round of in booth live demos showcasing how our solutions empower clinical and research labs: 📌 9:40 AM – Whole Genome Analysis with Long Read Data 📌 10:10 AM – Somatic NGS Testing: Simplifying cancer analysis with Oncogenicity Classifier & CancerKB 📌 1:10 PM – NGS Enterprise Capabilities: Automation, integration & data warehousing 📌 3:10 PM – PGx: Pharmacogenomics Workflow 🔗 Full details here: https://bit.ly/3XSFg0P Don’t miss out—stop by booth #722 to see how we’re helping labs streamline workflows and advance precision medicine. Looking forward to wrapping up ACMG with great discussions! #ACMGMtg2025 #Genomics #NGS #PrecisionMedicine #Bioinformatics #GoldenHelix

Day 2 at ACMG 2025 is here! If you haven’t stopped by booth #722 yet, today is the perfect time to see how Golden Helix is pushing the boundaries of NGS analysis and genomic data interpretation. We have another packed schedule of live demos showcasing how our solutions optimize workflows for clinical and research labs: 📌 10:15 AM – Whole Genome Analysis with Long Read Data 📌 11:30 AM – Somatic NGS Testing: Simplifying cancer analysis with Oncogenicity Classifier & CancerKB 📌 12:15 PM – Carrier Status Analysis in VarSeq 📌 12:45 PM – Calling CNVs in Whole Exomes 📌 3:15 PM – NGS Enterprise Capabilities: Automation, integration & data warehousing 📌 4:00 PM – PGx: Pharmacogenomics Workflow 🔗 Full details here: https://bit.ly/3XSFg0P Whether you're looking to streamline whole genome analysis, improve cancer diagnostics, or enhance pharmacogenomics workflows, we’ve got you covered. Stop by booth #722 and let’s talk precision medicine! #ACMGMtg2025 #Genomics #NGS #PrecisionMedicine #Bioinformatics #GoldenHelix

Kicking off ACMG 2025 today! If you're attending, swing by booth #722 to see our latest advancements in NGS analysis and genomic data interpretation. We have an exciting lineup of live demos in booth showcasing how our tools streamline workflows for clinical and research labs: 📌 5:15 PM – Whole Genome Analysis with Long Read Data 📌 5:45 PM – Somatic NGS Testing: Simplifying cancer analysis with Oncogenicity Classifier & CancerKB 📌 6:15 PM – Calling CNVs in Whole Exomes 📌 6:45 PM – NGS Enterprise Capabilities: Automation, integration & data warehousing 🔗 Full details here: https://bit.ly/3XSFg0P Stop by, grab a t-shirt, ask questions, and see how we’re advancing precision medicine. Looking forward to connecting with you! #ACMGMtg2025 #Genomics #NGS #PrecisionMedicine #Bioinformatics #GoldenHelix

Golden Helix is heading to Los Angeles for ACMG 2025! Join us at booth #722 to explore our latest enterprise genomics solutions for your NGS analysis pipelines. We have an exciting lineup of live demos at our booth—plus, all demo attendees get one of our brand-new t-shirt designs! 👕 We’re looking forward to a great meeting and connecting with you all in Los Angeles. See you soon! 🔗 Demo Schedule: https://bit.ly/3XSFg0P #ACMG #ACMGMtg2025 #GoldenHelix #Genomics #NGS

🖥️ We are pleased to invite you to an upcoming webcast. In it, we will explore VSWarehouse 3's capabilities in delivering a dynamic and flexible full-stack solution for Next-Generation Sequencing (NGS) data management. 💡 Key Topics to Be Covered: - Streamlining NGS data integration into a centralized and scalable platform - Real-world applications of VSWarehouse 3 in variant interpretation and clinical reporting - Features that enhance efficiency, accuracy, and data security This webcast is a valuable opportunity to gain insights into how VSWarehouse 3 can transform your NGS workflows and drive improvements in your clinical and research applications. #NGS #Bioinformatics #ClinicalGenomics #VSWarehouse3 #GoldenHelix #PrecisionMedicine

We're thrilled to announce a multi-year partnership with all Danish healthcare regions, advancing precision medicine on a national scale! By equipping Denmark’s laboratories with our advanced genomic technologies, we're driving innovation in genomic medicine to improve patient outcomes. Read more: https://yhoo.it/3FfdB3P #PrecisionMedicine #Genomics #ClinicalGenomics #NGS #Denmark #GoldenHelix

🧬Biomarker discovery is essential in rare disease diagnostics, providing critical insights into pathogenic variants that can guide clinical decision-making. However, translating genetic data into clinically actionable results requires a workflow that is both rigorous and adaptable to evolving guidelines. 💻VSClinical streamlines this process by delivering clinical-grade variant interpretation aligned with ACMG and AMP guidelines. By integrating biomarker discovery into a validated clinical workflow, we empower clinicians to provide more accurate diagnoses and improve patient outcomes. Learn more about VSClinical here: https://bit.ly/3sBpRFL #NGS #RareDisease #BiomarkerDiscovery #ClinicalGenomics

🌐🧬 Enterprise Genomic Analysis: Cloud & On-Premise Solutions As genomics continues to scale, organizations need efficient solutions to manage, analyze, and interpret large amounts of complex genomic data. In our latest webcast, we explored how VSWarehouse 3's enterprise-level genomic analysis can be deployed in both cloud and on-premise environments to maximize flexibility, security, and performance. Watch the recording to learn about: ✅ Scalable solutions for enterprise genomics ✅ Cloud vs. on-premise deployment: key considerations ✅ Streamlining genomic workflows for research & clinical use Watch now: https://bit.ly/41u6ygh #EnterpriseGenomics #GenomicData #NGS #NGSAnalysis #PrecisionMedicine

🧬 Next-generation sequencing enables personalized cancer therapy. The ability to identify relevant mutations in cancer allows clinicians to recommend relevant and targeted treatment options. Today, clinicians are moving beyond limited gene panels in order to capture the full spectrum of mutations. 🚀 Our software handles all NGS data types, from short-read and long-read sequencing data, and with the ability to scale from panels to genomes. With our VSClinical AMP tool, users can analyze and find drug matches for all relevant biomarker types as well, thus improving personalized cancer therapy. 🔗 Learn more about VSClinical AMP: https://lnkd.in/gQXtHB8F #NGS #CancerGenomics #PrecisionOncology #ClinicalGenomics #GenomicTesting #MolecularDiagnostics #CancerResearch #VSClinical

The future of genomic data management is here! Join us for an in-depth webcast on VSWarehouse 3, where we’ll explore how our cutting-edge solution is transforming enterprise genomic analysis—whether in the cloud or on-premise. 🔍 What You’ll Learn: ✅ Scalable data storage & management ✅ Streamlined variant analysis workflows ✅ Secure deployment options tailored to your needs Whether you're a clinical researcher, bioinformatician, or part of a precision medicine team, this webcast is designed to help you unlock the full potential of genomic data at scale. Don't miss out! #Genomics #Bioinformatics #PrecisionMedicine #CloudComputing #EnterpriseGenomics #GoldenHelix #NGS #NextGenerationSequencing