💡 It’s happening next week! You are invited to join our scientific lecture at the Variant Effect Prediction Training Course (VEPTC) by Human Genome Organization (HUGO) in Palermo! 🗓 Wednesday, October 16th ⏰ 5:00 PM - 5:45 PM From the early days of basic machine learning to today’s powerful deep learning, Artificial Intelligence has revolutionized how we analyze complex genomic data. But what does the future hold? Join us as our CSO Susanna Z. explores how AI has shaped and will continue to shape genomic variant interpretation—leading to higher accuracy and more efficient analysis! To know more: https://lnkd.in/dUqgWisW #enGenome #AIingenomics #VEPTC24 #ngsanalysis
enGenome
Sviluppo di software
Pavia, IT 5.298 follower
Genomic Variant Interpretation to the Next Level!
Chi siamo
enGenome provides experience and software technology for the analysis and interpretation of sequencing data in clinical and research settings. Our bioinformatics products leverage the power of artificial intelligence to deliver precise analyses, improving diagnosis and treatment processes for patients
- Sito Web
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www.engenome.com
Link esterno per enGenome
- Settore
- Sviluppo di software
- Dimensioni dell’azienda
- 11-50 dipendenti
- Sede principale
- Pavia, IT
- Tipo
- Società privata non quotata
- Data di fondazione
- 2016
- Settori di competenza
- Bioinformatics, Next Generation Sequencing, Healthcare e Genomic
Località
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Principale
Via Fratelli Cuzio, 42
Pavia, IT 27100, IT
Dipendenti presso enGenome
Aggiornamenti
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SIGU 2024 is in full swing! ⛳ Our workshop yesterday was a great success and we also presented 5 posters discussing our latest advancements. The engagement has been fantastic, and it's clear that innovation is at the forefront of everyone’s minds! 🧬 If you haven’t yet, make sure to stop by our booth #6 to have a chat with our team. #SIGU2024 #Genomics #enGenome #eVai #VarChat
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It's today! 🎉 🗓 For all SIGU attendees: Make sure to join us at 12:30 PM in Sala Giotto Balconata to learn how you can bring more efficiency and accuracy to your analysis by leveraging VarChat, the first AI-powered genomic assistant, and eVai, the state-of-the-art in variant interpretation. Our team is waiting for you! See you there 🧬 #engenome #SIGU2024 #eVai #VarChat
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We're excited to join SIGU – Società Italiana di Genetica Umana 2024 next week and share our AI-driven solutions for genomic interpretation. 📅 Join our workshop! Thursday, October 3, 12:30-13:30, Sala Giotto Balconata There we will present: 🧠 VarChat: The First AI-Powered Genomic Assistant – we'll show how VarChat rapidly retrieves scientific literature on human genomic variation to support interpretation. 🧬 eVai Suggested Diagnosis – see how our AI-driven platform leads the way in identifying and prioritizing causative variants for a more accurate and efficient interpretation. And don't forget to visit us at booth #6! See you in Padova! #SIGU2024 #Genomicshashtag #AIinHealthcarehashtag #VarChathashtag #eVai
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Frequent reanalysis slows down productivity and eats up valuable time. 🎯With eVai’s 98% classification accuracy and 4 variants to review on average per patient, you get reliable results right from the start, cutting down the need for repeated analyses. 🕒 This means less time wasted and fewer resources spent. Activate your free trial account: https://lnkd.in/dVkZMSM5 #eVai #ngsanalysis #bioinformatics #variantinterpretation
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📢 Calling out everyone who is attending the Training Course on Germline and Somatic Pharmacogenetics in Cagliari, Italy starting today September 12th. Our dear client, Dr. Laura Fontana, from ASST Santi Paolo e Carlo will be presenting today at 17:30h and during her presentation, she’ll showcase eVai’s powerful variant calling and searching functionalities, its CNV detection capabilities, and how it simplifies the PGx workflow with automated filtering of variants to support interpretation and haplotype definition in pharmacogenomics 🧬 ✨ Best of luck to Dr. Fontana! You can access the program here: https://lnkd.in/dtS-6XNG #Pharmacogenetics #PGx #GenomicAnalysis #eVai
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🍫 Last weekend, our team had a great experience at a chocolate factory lab in Torino - a city famous for its chocolates! We had the chance to know more about the fascinating world of chocolate creation, learning how new flavors are crafted and how good quality ingredients make all the difference. And yes, we also got hands-on, making our very own chocolate bars! The best part? Indulging in all that goodness together. It was a fun way to bond, be creative and celebrate teamwork💪 #TeamBuilding #enGenome #teamwork
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eVai seamlessly connects with Amazon S3, BaseSpace, and Element Catalyst to streamline your FASTQ-to-report workflow 🧬📄 This integration helps you save time, minimize manual errors, and focus on what truly matters—delivering accurate results faster to your patients. Start your free trial: https://lnkd.in/dVkZMSM5 #ngsanalysis #eVai #genomics #bioinformatics
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🔍💡VarChat is designed to simplify your report drafting process by using advanced AI to extract and summarize key variant information from scientific literature. With VarChat, you can streamline the creation of clinical reports, ensuring that critical insights are captured accurately and efficiently. Access now: https://lnkd.in/dGrJaNi8 #Genomics #ClinicalReports #AI #VarChat
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Too many manual processes in variant interpretation often slows down efficiency, causing delays and extending diagnostic times ⌚ 👉 A good AI-driven variant interpreter is designed to: 🔹Reduce bottlenecks: Automating workflows to manage larger sample volumes effortlessly. 🔹 Faster diagnostics: Cutting down on analysis time for quicker diagnostics. 🔹 Increase accuracy: Leveraging AI technology for more reliable pathogenic variant detection. Talk to our experts: https://lnkd.in/dVkZMSM5 #eVai #AIingenomics #bioinformatics #engenome #ngsanalysis