Discover the Latest Advances in Variant Classification and Interpretation Tools at Golden Helix's Booth at ACMG 2024
Join Golden Helix at the American College of Medical Genetics and Genomics (ACMG) 2024 conference and discover the latest advances in genetic research. This premier event brings together leading researchers, clinicians, and industry experts to share their insights on cutting-edge topics in medical genetics.
At Golden Helix's booth, you'll have the opportunity to learn more about our advanced genetic analysis tools. Our comprehensive suite of software solutions includes VarSeq, VS-CNV, VSClinical, VSPipeline, and VSWarehouse, which provide powerful and user-friendly options for genomic analysis and interpretation based on the ACMG and AMP Guidelines.
Stop by our booth to see a live demo of our software, learn about the latest features, and discuss how our tools can enhance your genetic research. Plus, by visiting our booth for a demo, you'll receive one of our famous t-shirts.
Don't miss this chance to discover the latest in genetic analysis tools and meet with our expert team at ACMG 2024. We look forward to seeing you there!
Find us in Booth #1313
Come check out our exciting product demos and meet with our team to discuss your needs in Booth #1313. Plus, don't miss the chance to score brand new t-shirts designed exclusively for ACMG demo attendees! See you there!
Demo schedule
Don't miss out on the chance to experience our advanced software solutions in action! Our expert Field Application Scientist team will be leading short software demos throughout the conference exhibition at our booth. Stop by to see how our powerful and user-friendly tools can help take your genomic analysis and interpretation to the next level.
- Wednesday, March 13:
- 5:40 pm - Whole Genome Analysis with Long Read Data
- 6:40 pm - Somatic NGS Workflow with VarSeq - Streamlining Tertiary Analysis with Oncogenicity Classifier and CancerKB
- 7:10 pm - Calling CNV with Twist Exome 2.0
- Thursday, March 14:
- 10:30 am - PGx: Pharmacogenomics Workflow
- 11:40 am - Somatic NGS Workflow with VarSeq - Streamlining Tertiary Analysis with Oncogenicity Classifier and CancerKB
- 12:20 pm - Carrier Status Analysis in VarSeq
- 12:40 pm - Calling CNV with Twist Exome 2.0
- 3:20 pm - NGS Enterprise Capabilities - Automation, Warehousing, Continuous Improvement
- 4:10 pm - PGx: Pharmacogenomics Workflow
- Friday, March 15:
- 9:40 am - Whole Genome Analysis with Long Read Data
- 10:10 am - Somatic NGS Workflow with VarSeq - Streamlining Tertiary Analysis with Oncogenicity Classifier and CancerKB
- 11:20 am - 11:50 am Exhibit Theater Talk (Theater 2): Unlocking Genetic Mysteries: Mastering Exome Analysis with VSClinical & VS-CNV
- 1:10 pm - NGS Enterprise Capabilities - Automation, Warehousing, Continuous Improvement
- 3:10 pm - PGx: Pharmacogenomics Workflow
Exhibitor Talk
Unlocking Genetic Mysteries: Mastering Exome Analysis with VSClinical & VS-CNV
Friday, March 15th, 11:20am, Theater 2
Presented by: Nathan Fortier, PhD, Golden Helix Director of Research
This talk will be discussing the sensitivity rate for the detection of known CNV events at all three probe densities, the impact of best-practice quality metrics and filters on sensitivity, how VarSeq’s CNV annotation capabilities can be leveraged to identify likely pathogenic CNVs, and the interpretation of clinically relevant CNVs using VSClinical.