candysraka.blogg.se - Qiagen clc genomics workbench

#Qiagen clc genomics workbench install#
#Qiagen clc genomics workbench software#
#Qiagen clc genomics workbench license#

With growing read length, NGS reads more and more often also include partial downstream adapter sequences at the read end. Avoid analysis error through improved adapter trimming

#Qiagen clc genomics workbench license#

Stay tuned for more: we are working on an improved user interface for the CLC License Server.

#Qiagen clc genomics workbench install#

Colleagues may install a Module and explore the results without needing a license at all as long as no tool is launched.Īll acquired Module licenses are released to the CLC License Server when the Workbench is closed. Workbenches return the Module license 4 hours after the last time a tool was launched,Įven if the user has not closed the Workbench.Workbenches now only request a Module license from the CLC License Server when a tool from a module is actually launched.Administrating network licenses and sharing module licenses with colleagues is now more flexible.

Good news for site license owners: We have improved sharing of Modules for CLC Workbenches. Share module network licenses more freely 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!.09 – Join us for a 90-minute training session for new users of QIAGEN IPA. QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings – All Regions – Jul.21 – 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 – Jul.FASTQ to final report: An ultra-fast workflow for comprehensive genomic profiling – Jul 14 – Join us to learn how DNAnexus and QIAGEN Digital Insights are partnering to develop an agnostic, end-to-end workflow for CGP that goes from.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.

#Qiagen clc genomics workbench software#

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.

Clinical Analysis and Interpretation Services.

Pharmaceutical Development Bioinformatic 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.

QIAseq panels | QIAGEN Digital Insights.

Clinical QKB (Clinical QIAGEN Knowledge Base).

COSMIC (Catalogue of Somatic Mutations in Cancer).

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.