QIAGEN CLC Genomics Workbench version 22 is here with exciting updates we’d like to share with you. Join this webinar to learn ways to take advantage of the latest improvements and get an overview of the many new tools now available. These include:
• Template workflows to get you started on RNA-seq and DNA-seq analyses
• An expanded range of tools for grouping and describing sequences in sequence lists
• Support for NGS data import from Amazon S3 and Illumina BaseSpace
• Import data generated by MGI/BGI systems
• Single-cell ATAC-seq and RNA velocity
• Fast long-read assembly for Oxford Nanopore and PacBio reads from large eukaryotic genomes
• Import RNA-seq expression data in a matrix format
• Homologous recombination deficiency (HRD) scoring and methylation profiling
Make sure to join this webinar to elevate your understanding of current bioinformatics trends and get an overview of the latest capabilities of QIAGEN CLC Genomics Workbench.
Can’t make it at this time? Don’t worry. Register now, and we will send you the on-demand recording to catch up on what you missed.
Click here to register.
