#QIAGEN CLC GENOMICS WORKBENCH CONTACT SOFTWARE#

QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings вЂ“ All Regions вЂ“ Jul.

21 вЂ“ 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 вЂ“ All Regions вЂ“ Jun.Clinical Oncology Summit: Part 1 вЂ“ Part 2 вЂ“ June 16 (North America) and June 21 (Europe) | Customer IвЂ¦ вЂ“ A free-to-attend, two-part virtual event exploring how diagnostic labs can lower the barrier to adopt large cancer genomic profiling.Human Somatic Mutation Database (HSMD) вЂ“ A new somatic database developed by QIAGEN that contains extensive genomic content relevant to solid tumors and hematological malignancies.QIAGEN OmicSoft вЂ“ Powerful cloud-enabled вЂomics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration.QIAGEN IPA вЂ“ Powerful tools to uncover the significance of data and identify new targets or candidate biomarkers within the context of biological systems.

#QIAGEN CLC GENOMICS WORKBENCH CONTACT SOFTWARE#

Introducing QCI Interpret One, clinical decision support software with professional i. QCI Interpret One вЂ“ Oncology variant interpretation just got more precise.Catalogue of Somatic Mutations in Cancer (COSMIC) вЂ“ Explore the impact of somatic mutations in human cancer with the worldвЂ™s largest and most comprehensive resource.Clinical Analysis and Interpretation Services.Pharmaceutical Development Bioinformatic Services.QIAGEN Discovery Bioinformatics Services.QIAGEN CLC Genomics Workbench вЂ“ QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow.Human Gene Mutations Database (HGMD) вЂ“ Solve more cases faster, with data you can trust using HGMD Professional, the gold standard for identifying inherited disease-causing mutati.QIAseq panels | QIAGEN Digital Insights.Clinical QKB (Clinical QIAGEN Knowledge Base).COSMIC (Catalogue of Somatic Mutations in Cancer).

Clinical Testing Solutions вЂ“ Deliver patient-specific reports for any NGS panel in minutes with on-demand, expert-curated content and professional interpretation service.Stop looking for a needle in a haystack вЂ“ Easily accelerate biomarker and target discovery by exploring and interpreting your data with intuitive, visual biomarker identification too.Single-Cell Genomic Solutions вЂ“ Explore our powerful solutions for the analysis and interpretation of single-cell gene expression analysis and genomics.Pharmaceutical Development вЂ“ Whether searching for clinically applicable biomarkers, designing a new companion diagnostic (CDx), or honing your study accrual and go-to-m.Research & Discovery вЂ“ Powerful digital insights to help you innovate, integrate and translate scientific results into impactful discoveries.

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