The workshop covers how to perform microbial genomics tasks such as AVS analysis, hybrid viral sequencing, whole genome taxonomies profile, and AMR detection. Share insights with the new Viewing Mode. Get the features that meet your research goals with our new licensing models developed for this v21 release. The module allows you to examine bacterial, viral, and eukaryotic (fungal) genomes and metagenomes. QIAGEN CLC Genomics has solutions for all your sequencing, NGS and ‘omics data analysis needs. The QIAGEN CLC Microbial Genomics Module offers tools and workflows for various bioinformatics applications, such as microbiome analysis, isolate characterization, functional metagenomics, and antimicrobial resistance characterization. Product Details The modules are cross-platform desktop applications that enhance the functionalities of CLC Genomics Workbench. It includes steps for demultiplexing, mapping and metadata handling, as well as downstream analysis options. Specifically, you’ll learn how to: -Interpret the results using the interactive graphics produced by the workflows. Together we’ll explore how to import, analyze and interpret your NGS data. to 3 p.m.), focuses on microbial genomics data analysis. This tutorial uses the capabilities of CLC Genomics Workbench with the Biomedical Genomics Analysis plugin to analyse UPX 3 reads and assess quality. In this training, we’ll use QIAGEN CLC Genomics Workbench to analyze immune repertoire NGS data generated from RNA-seq or single-cell RNA-seq data. The afternoon session, Exploring Microbial Genomics with CLC Genomics Workbench (1 p.m. Register for the in-person session of CLC Genomics Workbench Overview (Falk Library, Classroom 2).Register for the online session of CLC Genomics Workbench Overview (Zoom meeting link will be shared via email).It also highlights what’s new in version 23.02, such as super-fast fastq to VCF read mapping, bulk RNA seq improvements, single-cell analysis tools, and more. to noon) introduces CLC Genomics Workbench and its features, such as unique read mapping and de novo assembly, resequencing workflows, ChIP-seq and RNA-seq applications, and more. The classes are led by Shawn Prince, Qiagen’s senior field application scientist.ĬLC Genomics Workbench Overview (10:30 a.m. HSLS MolBio invites you to learn more about how CLC Genomics Workbench can assist you with your NGS data analysis projects through two workshops on Wednesday, March 22, 2023. YouTube WebQIAGEN CLC Genomics Workbench QIAGEN CLC Genomics Workbench is a. HSLS has had an institute-wide access license for CLC Genomics Workbench since 2014 new features of the software are now available in the recently released version 23.02. CLC Manuals - Transcript Discovery using CLC Genomics. Posted about my SAB listing a few weeks ago about not showing up in search only when you entered the exact name. Understand management of reference dataģ.CLC Genomics Workbench is a powerful analysis tool for genomics, transcriptomics, and epigenomics research. Learn to work with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI)Ģ. 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. 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. Powered by cutting-edge technology and accelerated algorithms, it supports a comprehensive set of NGS data analysis applications. QIAGEN CLC Genomics Workbench is a powerful solution to analyze and visualize next generation sequencing (NGS) data.
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