Discover the new AI/machine learning-enabled Coronavirus Network Explorer, built from the IPA Knowledge Base. This freely available tool helps you visualize how SARS-CoV-2 proteins interact with human host proteins to disable protective responses and pathways and explore hypotheses around how to fight #coronavirus. ⬇️
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🤯 Just got incredible insights on knowledge bases from QIAGEN here at #BioITExpo booth 620! Bio-IT World #DoYouAI #OmicSoft #BiomedicalKB
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🤝 Connect with QIAGEN at booth 96 on #swissbiotechday in Basel, Switzerland! We’ll be sharing how you can bridge data and discovery by using high-quality and high-volume biomedical datasets, accelerating drug discovery. Talk to you then! #BiomedicalKB #DoYouAI️ Swiss Biotech Association
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👩⚕️👨⚕️ Join QIAGEN at the Nordic #PrecisionMedicine Forum 2024 on April 22–23 in Stockholm, Sweden! Attend our talks to learn how you can future-proof your NGS lab with our products: ☑️ #QIAseq Multimodal DNA/RNA Library Kit: Our new easy-to-use, single-tube DNA and RNA library kits maximize yields while providing streamlined protocols for high-throughput purification ☑️ #QCI Interpret for Oncology: This tool eliminates the need for complex bioinformatics pipelines, reducing turnaround time and simplifying variant interpretation for confident decisions. Learn more or schedule your personalized demo now ⬇️ #NPMF2024
Join QIAGEN at NPMF 2024 in Stockholm, Sweden
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⚕️ Don’t miss QIAGEN at the AI and Data in Pharma Healthcare Summit in Munich, Germany! Learn how you can leverage our unique blend of expert-curated and generative AI-derived biomedical knowledge, which lets you hit the ground running with drug discovery. Learn more 👇 #BiomedicalKB #DoYouAI
Learn about our Biomedical KBs at AI and Data in Pharma Healthcare Summit
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🙅 Don’t let variant identification errors slow your research down. Our top-of-the-line software #QCI IT and knowledge bases #COSMIC and #HGMD let you gain valuable and reliable insights into your disease-relevant variants without the struggle. Join our webinar tomorrow to learn more 👇
Say no to errors in variant identification – join us
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⏰ Monday marks #BioITExpo 2024! Get the latest on #biotech and learn how to leverage our knowledge bases in #drugdiscovery and #biopharma research. We’ll showcase the two flavors of our biomedical KBs, made unique by their causal content, and our one-of-a-kind unified ‘omics repository: ⭐ Biomedical KB-HD: expert-curated, with over 24M relationships and API access ⭐ Biomedical KB-AI: generative AI-derived, with over 643M relationships ⭐ OmicSoft: expert-curated ‘omics datasets with a unified ontology Schedule your personalized demo now ⬇️ See you in Boston! #BiomedicalKB #OmicSoft #DoYouAI Bio-IT World
Join us at Bio-IT World 2024 in Boston, MA
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🎉 QIAGEN Ingenuity Pathway Analysis (#QIAGENIPA) Spring 2024 Release is here! While this release shows explosive growth in findings and datasets for Analysis Match, you also get customizable Canonical Pathway heatmaps in Comparison Analyses and changes to LINCS datasets and IPA functions. Learn more ⬇️
See what's new with the IPA Spring 2024 Release
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🤨 When free seems too good to be true, that’s because it usually is. Read our blog post to find out what free pathway analysis tools can get you vs. premium ones like QIAGEN Ingenuity Pathway Analysis (#QIAGENIPA) – and whether the zero price tag is really worth it 👇
Blog | How much do you really save with free pathway analysis?
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😎 Get variant annotation right every time by attending this masterclass! 💪 On April 16, learn how to leverage our comprehensive, expert-curated knowledge bases Catalogue of Somatic Mutations in Cancer (#COSMIC), Human Gene Mutation Database (#HGMD) and all-in-one NGS variant interpretation software #QCI Interpret Translational (QCI IT) and accelerate your #somatic and #germline variant research. Join us 👇
Join our variant interpretation masterclass
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🤩 Discover effective strategies to avoid variant misinterpretations in your #diagnosticLab in 2024 – on your own time! In this on-demand webinar, Dr. Ana Krivokuca, head of the Department of Genetic Counseling at the Institute of Oncology and Radiology of Serbia, presents three neurological disorder case studies that used #HGMD Pro's gold-standard germline data to link phenotypes to causative variants, identify and interpret clinically relevant variants, discover ethnically relevant variants and develop #NGS #genepanels with confidence. Watch it now 👇
On-demand webinar | Case studies: Mitigating errors in variant interpretation
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