QIAGEN CLC Genomics Workbench is a powerful solution to analyze and visualize next generation sequencing (NGS) data. Powered by cutting-edge technology and accelerated algorithms, it supports a comprehensive set of NGS data analysis applications.
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. 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.
1. Learn to work with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI)
2. Understand management of reference data
3. Use algorithms for read trimming, mapping, de novo assembly and variant calling