Lasergene 17.1 Release Notes

New Workflows and Visualization Options for Sanger, NGS, and Long Read Assemblies (SeqMan Ultra and SeqMan NGen)

• Automated assembly of Sanger/ABI samples with easy multi-sample Sanger variant analysis and visualizations
• Option for quick Sanger assembly setup or guided step-by-step setup for more advanced projects
• A  unique, multi-sample visualization of assembled sequences makes it easy to view and compare multiple assemblies in a single project
• A new retrovirus integration workflow automates the precise locating of prophage and retrovirus insertion sites in the host genome during alignment
• Improvements to the live variant report allow you to visualize variants in the alignment view in real-time, as filters are applied
• New option for combining multiple projects of the same type into a single project
• De novo assembly of Oxford Nanopore and PacBio long read sequencing data, with or without short read correction (beta)