![]() ![]() Transcriptomics Data analysis on CLC Genomics Workbench. This tutorial uses tools available in the Genomics Workbench 7.5. Build-in modules for reference mapping, variant calling and de novo assembly. Workbench versions To create a workflow, you must be working with the CLC Genomics Workbench, version 5.5 or higher. Understand management of reference dataģ. We will briefly introduce the CLC genomics workbench, a. We will be putting together a workflow that includes mapping reads to a reference, detection of variants and filtering of these variants for common ones. Learn to work with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI)Ģ. Clc genomics workbench map to reference mac#Learn about: Working with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI) Tailored solutions for RNA-seq, DNA-seq and methylation Efficient algorithms for read trimming, mapping, de novo assembly and variant calling Effective management of reference data Scalable processing of many samples, with advanced workflow and reporting capabilities Easy installation on Windows, Mac and Linux.ġ. 1:00pm 1:30pm: Overview of the Microbial Genomics/Metagenomics Applications in the CLC Genomics Workbench. Some tools and functions require that the database attribute is assigned or that a Custom Reference Genome is set up as a Custom Build prior to use. In this live webinar, Leif Schauser, Ph.D., Director Product Management Genome Analysis, will review a host of new features in the latest release of the QIAGEN CLC Genomics Workbench 20 that help you scale your research, and allow you to ramp up your productivity by taking your multi-sample analyses to the next level. Map reads to reference Peak calling and annotation Variant calling, annotation, filtering and comparison 12:00pm 1:00pm: Lunch provided by QIAGEN. All the tools you need, integrated into a single user friendly and scalable application, and ready to generate results you can trust. Powered by cutting-edge technology and accelerated algorithms, it supports a comprehensive set of NGS data analysis applications. CLC Genomics Workbench (CLC Gx) is a powerful solution developed by scientists for scientists to analyze and visualize next generation sequencing (NGS) data. ResearchGate has not been able to resolve any references for this publication. QIAGEN CLC Genomics Workbench is a powerful solution to analyze and visualize next generation sequencing (NGS) data. CLC Genomics Workbench 7 and CLC M icrobial Genome Finishing Module. ![]()
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