Discover the Latest Advancements in Variant Classification and Interpretation Tools at Booth 1500 during AMP 2023
Join Golden Helix at the AMP 2023 conference and delve into the latest advancements in genetic research. This gathering convenes renowned researchers, clinicians, and industry pioneers to share insights on the cutting-edge topics in human genetics.
At Golden Helix's booth, immerse yourself in our top-tier genetic analysis tools. Our extensive portfolio of software solutions encompasses VarSeq, VS-CNV, VSClinical, VSPipeline, and VSWarehouse, providing robust and intuitive avenues for genomic analysis and interpretation in line with the ACMG and AMP Guidelines.
Step up to our booth for a live demonstration of our software, uncover the newest features, and converse about how our tools can elevate your genetic research. Plus, by engaging in our booth demo, you'll get your hands on one of our exclusive t-shirts.
Embrace this chance to discover the forefront of genetic analysis tools and interface with our adept team at AMP 2023. We're eager to connect with you!
Find us at Booth #1500
Make it a point to drop by Booth #1500 for engaging product demonstrations and to discuss with our team about your unique requirements. Also, don't miss out on our freshly designed t-shirts, made exclusively for AMP demo visitors! We're looking forward to seeing you!
Demo schedule
Don't miss out on the chance to experience our advanced software solutions in action! Our 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.
- Thursday, November 16:
- 11:55 - Automation of Clinical NGS Testing with VarSeq and VSWarehouse
- 2:20 - AMP Guideline Based Somatic NGS Workflow with VarSeq and VSClinical
- 2:55 - Carrier Status and Hereditary Cancer Testing Analysis in VarSeq
- 3:40 - Golden Helix CancerKB: Report Ready Curations to Support the AMP Guidelines
- 4:30 - NGS Copy Number Variant Calling and Interpretation: A Complete Clinical Workflow
- 6:10 - TSO500 and Tackling the Complexity of Comprehensive Genomic Profiling
- Friday, November 17:
- 9:10 - TSO500 and Tackling the Complexity of Comprehensive Genomic Profiling
- 9:45 - NGS Copy Number Variant Calling and Interpretation: A Complete Clinical Workflow
- 11:55 - Golden Helix CancerKB: Report Ready Curations to Support the AMP Guidelines
- 12:40 - 1:10 Innovation Spotlight (Stage 2): Comprehensive Genomic Profiling in Oncology: Apply the AMP Guidelines for TSO-500 Variant Analysis and Clinical Reporting
- 2:55 - Carrier Status and Hereditary Cancer Testing Analysis in VarSeq
- 3:15 - AMP Guideline Based Somatic NGS Workflow with VarSeq and VSClinical
- 3:45 - Automation of Clinical NGS Testing with VarSeq and VSWarehouse
- Saturday, November 18:
- 9:10 - AMP Guideline Based Somatic NGS Workflow with VarSeq and VSClinical
- 9:35 - Golden Helix CancerKB: Report Ready Curations to Support the AMP Guidelines
- 10:00 - TSO500 and Tackling the Complexity of Comprehensive Genomic Profiling
- 11:55 - Automation of Clinical NGS Testing with VarSeq and VSWarehouse
- 12:20 - Carrier Status and Hereditary Cancer Testing Analysis in VarSeq
- 12:50 - NGS Copy Number Variant Calling and Interpretation: A Complete Clinical Workflow
As an industry leader in NGS technologies, we understand the importance of providing tailored solutions to meet the specific needs of each lab. Schedule a one-on-one meeting at AMP with our President & CEO, Andreas Scherer, to discuss your lab's specific challenges and goals. He will provide expert insights and guidance on how our company can best support your lab in achieving its goals. This is a valuable opportunity to gain a deeper understanding of how we can work together to achieve success.
Innovation Spotlight
Comprehensive Genomic Profiling in Oncology: Apply the AMP Guidelines for TSO-500 Variant Analysis and Clinical Reporting
Friday, Novemebr 17th, 12:40, Stage 2
Presented by: Gabe Rudy, VP of Product & Engineering
The session "Comprehensive Genomic Profiling in Oncology" focuses on utilizing VarSeq software to adhere to AMP guidelines for TSO-500 variant analysis and clinical reporting. As molecular oncology progresses, the need for sophisticated tools to interpret genomic data for personalized medicine becomes crucial. VarSeq addresses this by automating the analysis of large multi-omics panels, such as the TSO-500, facilitating the scaling of laboratory operations. The discussion delves into evaluating and reporting genomic signatures like MSI, TMB, PD-L1, and HRD in line with AMP standards. VarSeq enhances efficiency through an automated scoring algorithm that filters somatic variants, streamlining oncogenicity assessments. Additionally, Golden Helix's CancerKB is highlighted for its report-ready interpretations, which include multi-biomarker insights, tumor-specific therapies, gene-level cancer markers, and clinically significant negative results. This session promises insights into VarSeq's advancements that are transforming genomic data interpretation in oncology.