From Calling to Comparison Webinar

Hosted by DNASTAR experts Thomas Leary (Genomic Support Specialist) and Matt Keyser (Senior Product Manager), this live demo is useful even if you’re new to Lasergene. You’ll learn how to:

• Utilize the highly accurate GATK haplotype caller.
• Visualize paired tumor-normal experiments with MuTect2, leveraging GnomAD data and controls.
• Manage, filter, and compare variants across multiple samples within GenVision Pro and take advantage of its new on-the-fly database that lets you easily add/remove experiments from comparisons and recompute variants.
• Import and compare variants from single or multi-sample VCF files against assemblies or other VCFs.
• Perform long-read structural variation analysis, accurately identify indels, calculate insertion lengths, and assemble insertions de novo.