However, allelic variation, particularly cryptic (unknown or not annotated) variation, is problematic for follow up analyses. On-demand webinar: Harnessing insight from real-world oncology cases : introducing HSMD – In this on-demand webinar, we will introduce you to the Human Somatic Mutation Database (HSMD)-a new somatic database developed by QIAGEN.Allelic variation is the cornerstone of genetically determined differences in gene expression, gene product structure, physiology, and behavior.On-demand Webinar: How you can simplify your NGS secondary analysis workflow to 5 easy steps – Find out how you can simplify your NGS secondary analysis workflow to 5 easy steps using QCI Secondary Analysis, a new cloud-based service f.On-demand webinar: Discover hidden relationships in your toxicological studies with QIAGEN IPA – Watch this informative past webinar on how QIAGEN IPA can help you dig deeper into your toxicogenomic studies!.
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30 – In this live panel discussion, experts in NGS testing and clinical informatics explore issues in standardizing variant interpretation. Mitigating Variability in Somatic Variant Interpretation: An Expert Panel – Sep.01 – Join us for a 90-minute training session for new users of QIAGEN IPA. QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings – All Regions – Oct.19 – As requested by many users, QIAGEN Digital Insights team is excited to introduce QIAGEN Ingenuity Pathway Analysis (IPA) deep-dive trainings. QIAGEN Ingenuity Pathway Analysis (IPA): Deep-dive trainings – All Regions – Oct.
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13 – Learn how to build a next-gen software workflow for germline testing, as part of the Hereditary NGS Clinical Summit Series, a two-part, free.
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Introducing QCI Interpret One, clinical decision support software with professional i. QCI Interpret One – Oncology variant interpretation just got more precise.Catalogue of Somatic Mutations in Cancer (COSMIC) – Explore the impact of somatic mutations in human cancer with the world’s largest and most comprehensive resource.Pharmaceutical Development Bioinformatic Services.Clinical Analysis and Interpretation Services.QIAGEN Discovery Bioinformatics Services.QIAGEN CLC Genomics Workbench – QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow.Human Gene Mutations Database (HGMD) – Solve more cases faster, with data you can trust using HGMD Professional, the gold standard for identifying inherited disease-causing mutati.Clinical QKB (Clinical QIAGEN Knowledge Base).COSMIC (Catalogue of Somatic Mutations in Cancer).QIAGEN CLC Genomics Workbench (Desktop).Learn more about its role in oncogenesis and ac. Know your biomarkers: PRKD1 linked to head and neck cancer? – A new cancer gene, PRKD1, has been identified as defining a subset of head and neck cancers.Stop looking for a needle in a haystack – Easily accelerate biomarker and target discovery by exploring and interpreting your data with intuitive, visual biomarker identification too.Single-Cell Genomic Solutions – Explore our powerful solutions for the analysis and interpretation of single-cell gene expression analysis and genomics.Pharmaceutical Development – Whether searching for clinically applicable biomarkers, designing a new companion diagnostic (CDx), or honing your study accrual and go-to-m.Research & Discovery – Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.
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