![]() When shown in circular view, it is no longer displayed as a joined annotation over the start point but as a continuous annotation.Before, there was a line from beginning to end of the annotation, and this has now been removed. When shown in linear view they have a cleaner appearance.Rename can now be done through right-click menu in Navigation Area.Performance when sorting of large tables has been improved.Note that the Side Panel settings are only copied to the new view if they have been changed by the user in the old view. As an example: if you have specified a set of restriction enzymes to display in the circular view of a sequence and switch to the linear view, these enzymes will also be listed in the Side Panel here. Relevant view settings are now copied when switching between different views of the same data.Quick launch of tools: Pressing Ctrl + Shift + T shows a dialog for easy typing and launching tools.Favorite tools: Right-clicking a tool in the Toolbox allows you to add a tool to your favorites list.This is automatically updated based on which tools are used most frequently. New Favorite Toolbox: A new tab next to the Toolbox holds.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.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!.23 – Join us for a 90-minute training session for new users of QIAGEN IPA. QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings – All Regions – Nov.10 – An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trend. Hereditary NGS Clinical Summit Series: Part II – Nov.24 – 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 – Nov.QIAGEN OmicSoft – Powerful cloud-enabled ‘omics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration.Human Somatic Mutation Database (HSMD) – A new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies.QIAGEN IPA – Powerful tools to uncover the significance of data and identify new targets or candidate biomarkers within the context of biological systems.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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