Maximizing Insights from Multi-Sample Variant Analysis

To see these features in action, watch our 1-hour on-demand webinar presented by DNASTAR Senior Product Manager, Matt Keyser. This webinar assumes no prior knowledge of Lasergene software. Matt demonstrates how to:

• Create single-sample and multi-sample variants tables, as well as a table of structural variations.
• Filter variants based on a Venn diagram, on single or multiple baseline controls, on paired samples (e.g., normal vs. tumor), on the percentage of samples containing the variant, and many other options. Save a filter or set it as the default filter for future projects.
• Create sets of variants and compare them with other saved sets.
• View the results of a SeqMan NGen assembly in which long-read variants data has been separated by haplotype (phased), and identify any compound heterozygous mutations.