#INTRODUCTION TO CLC GENOMICS WORKBENCH HOW TO#
#INTRODUCTION TO CLC GENOMICS WORKBENCH SOFTWARE#

FASTQ to final report: An ultra-fast workflow for comprehensive genomic profiling вЂ“ Jul 14 вЂ“ 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.13 вЂ“ Join us for a 90-minute training session for new users of QIAGEN IPA. QIAGEN Ingenuity Pathway Analysis (IPA) New user trainings вЂ“ All Regions вЂ“ Jul.QIAGEN OmicSoft вЂ“ Powerful cloud-enabled вЂomics GUI, complete NGS analysis workflows and unparalleled curated content for immediate exploration.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 IPA вЂ“ Powerful tools to uncover the significance of data and identify new targets or candidate biomarkers within the context of biological systems.

#INTRODUCTION TO CLC GENOMICS WORKBENCH 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).

Learn more about its role in oncogenesis and ac.

Know your biomarkers: PRKD1 linked to head and neck cancer? вЂ“ 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 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.

The software covered in the workshop operates through a user-friendly, point-and-click graphical user interface, so neither programming experience nor familiarity with the command-line interface is required.

visualize data by generating PCA and heatmapsД®xperimental biologists seeking to analyze bulk RNA-Seq data generated through experiments or retrieved from a repository such as GEO.

perform differential expression analysis.

estimate known gene and transcript expression.

import RNA-Seq FASTQ reads from a GEO dataset.

access the CLCbio Genomics ServerВ hosted on the HTC ClusterВ by Pitt CRC.

The workshop lecture video will walk you through the steps of a bulk RNA-seq data analysis process using the HSLS-licensed CLC Genomics Workbench.

#INTRODUCTION TO CLC GENOMICS WORKBENCH HOW TO#

During this virtual hands-on session, you will learn how to solve the exercise problems.

This is a flipped class links to PowerPoint slides, lecture videos, and practice exercises that you can view on your own schedule are available upon registration. Register for RNA-Seq Data Analysis using CLC Genomics Workbench

Introduction to clc genomics workbench