Maximizing Insights from Multi-Sample Variant Analysis
Matthew Keyser
Senior Product Manager
The recent release of Lasergene 18 includes numerous enhancements for multi-sample variant analysis in GenVision Pro, including advanced variant filtering, specialized displays for phased variants, and the ability to create and compare custom SNP sets.
To see these features in action, register for our live 1-hour webinar, to be held on Wednesday, November 13th at 11:00 am CDT. Presented by DNASTAR Senior Product Manager, Matt Keyser, this webinar assumes no prior knowledge of Lasergene software. Matt will demonstrate 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.
If you have any questions, Matt will be happy to answer them at the end of the webinar. All registrants will also receive a link to the webinar recording after the live event.
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