#CLC GENOMICS WORKBENCH CITATION HOW TO#
#CLC GENOMICS WORKBENCH CITATION SOFTWARE#

The findings were significant not only because of the major threat of viral disease to both avian and human species, but also because they were robust: the team used two or more technologies to detect 128 genes from a compiled, curated list of 193 potentially anti-viral genes. Chicken Interferome: Avian Interferon-Stimulated Genes Identified by Microarray and RNA-seq of Primary Chick Embryo Fibroblasts Treated with a Chicken Type I Interferon (IFN-α)Įarlier this year, Veterinary Research ran a report by a team from the Imperial College of London studying the interferon response in virus-infected chickens. Read on for details from some recent publications. We enjoy learning how it’s being used to support a wide range of NGS bioinformatics applications, from veterinary research to wastewater treatment. CLC Genomics Workbench is developed by scientists, for scientists, to analyze and visualize next generation sequencing (NGS) data. Genome research scientists want a powerful, end-to-end solution that easily integrates into their existing NGS analysis workflows. Publications citing CLC Genomics Workbench 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!.21 – Join us for a 90-minute training session for new users of QIAGEN IPA. QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings – All Regions – Aug.23 – This training will focus on using IPA and HSMD to identify key somatic variants associated with regulatory genes in ‘omic data. Somatic variants investigation in context of critical regulatory pathways and networks – Aug.

#CLC GENOMICS WORKBENCH CITATION HOW TO#

16 – Join us in this training to learn how to locate public single-cell studies of their interest using Omicsoft Single Cell Lands.

Public single cell RNA-seq data investigation using Omicsoft and Ingenuity Pathway Analysis – Aug.

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.

#CLC GENOMICS WORKBENCH CITATION 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.

Clc genomics workbench citation