![]() 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.The slides from the presentations of Holger Karas will be uploaded soon. Please find below the slides of the presentations that were given at the workshop. This will help us to learn on how to improve future workshops. Please take a minute and provide us some feedback about CLC workshop. If you would like to contact the Qiagen support, then please write to the following email feedback about the CLC workshop You can download the sample data from the CLC Bio website: Participants who wish to use the CLC Genomics Server on the Euler cluster should contact cluster support one week before the workshop. This software can be downloaded from the IT Shop of ETH. Hands-on sessions require that participants bring their own laptop with CLC Genomics Workbench 9.0.1 installed. However the organizers reserve the right to accept or deny registrations to ensure that a single group does not monopolize the workshop. Registrations will be granted on a first-come, first-served basis. Please register here.ĭue to space reasons, the number of participants is limited to 60. Walk through IVA with a look at QCI (part 2) and introduction to IPAĪttendance is free for members of ETH, but registration is required. Walk through IVA with a look at QCI (part 1) Quick presentation of biomedical workbench / server including IVA / IPA integration Infrastructure, how to optimize usage of the server Toolbox and running some examples depending on the interest Introduction to the Workbench, plugins and connection to the server The workshop will take place on 23-24 November 2016 in the LEE building of ETH (room E101). The IT Services of ETH and Qiagen/CLC Bio are organizing a two-day workshop about CLC Genomics Workbench & Server. ![]()
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