Nostos Genomics

🎉 Streamline Your Variant Analysis Workflow 🎉 We’re excited to unveil our latest product release, now introducing our secondary analysis service integrated with AION - Our AI-powered variant interpretation tool! Our secondary analysis service reduces your requirement to invest in your own technology infrastructure and simplifies the complex variant interpretation process - providing an efficient, streamlined software solution for you 👉 From raw sequencing data to meaningful clinical insights, we’ve got you covered. 👉 A seamless solution which reduces manual steps, enabling the labs we work with to reduce diagnostic turnaround times 🔬 Ready to see the difference? Click here to discover your eligibility and get access to the platform https://lnkd.in/eNUVP9sG Want to discuss further? Arrange a call here https://lnkd.in/efnQXaZH #Genomics #SecondaryAnalysis #VariantInterpretation #PrecisionMedicine #Bioinformatics #ClinicalGenomics #NGS

It was great to attend the 15th NACG Workshop last week in Oslo. Our Co-founder and CTO Rocío Acuña Hidalgo participated in the "Bridging the gap - experiences with AI-solutions" session, where she shared the learnings from Nostos Genomics with AION (Our AI-driven variant interpretation solution) to identify novel disease-causing variants in diagnostics and research (more on this soon!). 🧬🔎📊 It was great to connect, meet so many people and learn more about the advances and challenges on the clinical implementation of genomics in the Nordic countries. A big thank you to all those that attended, and to the organisers for another excellent program! 🎉 #genomics #PrecisionMedicine #NostosGenomics #NordicAlliaceOfClinicalGenomics #NACGworkshop #NACG

👀 If you are attending the 15th NACG workshop in Oslo this week, don’t miss Rocío Acuña Hidalgo workshop session discussing how AI can help identify novel disease-causing mutations in diagnostics and research - Friday September 27th, at 09:00-10:00. Want to arrange a meeting with our team at the event? - Reach out here: https://lnkd.in/ePJFW7j2 #genomics #PrecisionMedicine #bioinformatics #NostosGenomics #NordicAlliaceOfClinicalGenomics #NACGworkshop #NACG

Join us at the 15th NACG workshop in Oslo, hosted by the Nordic Alliance for Clinical Genomics! Our team - including our CTO and Co-founder Rocío Acuña Hidalgo and Aina Pi Roig our Clinical Customer Success Manager - would love to talk to you about our latest product updates and exciting new projects. 👀 If you are attending the event, don’t miss Rocío Acuña Hidalgo workshop session discussing how AI can help identify novel disease-causing mutations in diagnostics and research - Friday September 27th, at 09:00-10:00. Want to arrange a meeting with our team at the event? - Reach out here: https://lnkd.in/ebx54ekX #genomics #PrecisionMedicine #bioinformatics #NostosGenomics #NordicAlliaceOfClinicalGenomics #NACGworkshop #NACG

🎉 We’re thrilled to announce that in our next product release, we will be introducing our secondary analysis service integrated with AION - Our AI-powered variant interpretation tool 🔬 👉 Simplify your workflow, reduce manual processes, and focus on what matters most – interpretation and discovery 👉 Secondary Analysis (FASTQ to VCF) with AION’s integrated secondary analysis pipeline 👉 Designed to give labs the data analysis speed they need to optimise the efficiency of processing their NGS data sets 👩🔬 Curious to learn more? Check your eligibility and get early access to the platform https://lnkd.in/gSAUh8SJ Want to discuss further? Arrange a call here https://lnkd.in/gE_GCvgp #GenomicResearch #VariantScientists #IntegratedAnalysis #WorkflowOptimization #SecondaryAnalysis #VariantAnalysis

👀 As this interesting article from Genomics England shows, previously classified genetic variants play a crucial role in future diagnostics. So how does your lab ensure that past classifications are accessible and useful? With AION - our AI-driven variant interpretation solution - our manual variant classification feature allows scientists to store, find and revisit previous classifications. This provides a foundation for faster, more accurate diagnoses, saving time while ensuring consistency across teams. 🙌 https://lnkd.in/eFFqwHJy Learn more about how AION can bring speed and efficiency to your workflow. Book a demo with our team! https://lnkd.in/eTNR8S8u #Genomics #AION #PrecisionMedicine #VariantClassification #ClinicalDiagnostics #Bioinformatics

🔬🚀At Nostos Genomics we were very excited and honoured to be invited to attend this years #UndiagnosedHackathon event (A great initiative by the Wilhelm Foundation). 120 people from around the world - Experts, patients and patient advocates diving into genomic data, using analytical methods, AI and innovation to solve previously undiagnosed cases. 👉 In case you missed it, Our CTO Rocío Acuña Hidalgo was recently interviewed where she discusses the history of Nostos Genomics, her involvement at the Undiagnosed Hackathon and the importance of finding diagnoses for patients. 🙌 https://lnkd.in/eYu8DUyx #undiagnosed #diagnosis #UndiagnosedHackathon #rarediseases #UndiagnosedHackathon2024

🧬 Meet Ritu Chandra our ‘Senior Product Designer’ - Over the last decade Ritu has worked as a product designer leading B2B and Enterprise Design products in information-intensive fields such as data science, fintech,healthcare and legal tech. In her role at Nostos Genomics, she focuses on developing a design vision for the company, discovering problem areas and possible solutions, enhancing the product from end users’ perspective and executing the design strategy. When we asked what they love about the industry and their role, she said, “Genomics is a complex, purpose driven, and beautiful field to be in. It’s exciting to see how the research, ways of working and the industry landscape are evolving with time. There are tremendous opportunities for learning and problem solving. Additionally, interacting with geneticists has been one of the most rewarding experiences because they’re some of the most sincere and passionate individuals I’ve met” 🧬 👀 Find out more about our team and what we do, here: https://lnkd.in/eCfqUjSv 👀 We’re always on the lookout for exceptional talent. Keep an eye on our careers page to find out more https://lnkd.in/eHzTbFdp

👀✨Did you know? AION has a database feature (AION DB) which means you can see insights generated from all your previous cases, helping you and your team find diagnoses quicker - Bringing the speed and efficiency of AI-prioritisation to your workflow! ✨ This capability means that AION will: 👉 Remember all of the variants it sees and provides you valuable insights of variant statistics 👉 Allow you to assign final classifications to your variants and leverage these decisions on future cases 👉 Allow you to incorporate this data in your advanced filtering strategies for improved efficiency and diagnostic yield Interested in learning more and seeing this in action? Click the link here - https://lnkd.in/gvg4NCG8 Read more about it here - https://lnkd.in/gkfswSaQ

🙏Thank to all of those who took part in our recent survey. We got some great insights from all sorts of stakeholders involved in interpreting genetic variants when trying to find diagnoses for patients. The winner of the prize went to Héctor San Nicolás Fernández 🎉 Thanks to everyone who took part and 🙌 to you Héctor San Nicolás Fernández! #RareDisease #ClinicalGenetics #variantscientist #genetictesting #precisionmedicine