ACMG Annual Meeting 2025

March 19–21, 2025

Los Angeles Convention Center | Los Angeles, CA USA

Visit us at Booth #433 to learn more about Thermo Fisher Scientific's rapid sample-to-answer solutions for next-generation sequencing (NGS) and microarray.


Exhibit theater presentation

We invite you to attend an educational session featuring Ludmilla Francescatto, PhD, Duke University, who will be evaluating Thermo Fisher’s CytoScan HD Accel microarray for research use.

 

Title Date Time Speaker Location
Using the Thermo Fisher CytoScan HD Accel—Duke’s Experience and Case Study Review Thursday, March 20 10:45–11:15 am

Ludmila Francescatto, PhD
Assistant Director, Division of Molecular Pathology, Genetics and Genomics

Assistant Professor, Pathology

Duke University

Exhibit Theater 2

Targeted NGS for a broad range of applications including inherited diseases and reproductive health research.
  • Ion GeneStudio S5 systems enable fast and scalable NGS with just 45 minutes of hands-on time from nucleic acid to report
  • Build targeted gene-panels from 5,000+ pre-tested genes or choose from off-the-shelf pre-designed assays with Ion AmpliSeq NGS panels
  • PGT-A and PGT-M testing from a single sample using a simple, integrated NGS workflow for any lab, regardless of expertise
  • Increase carrier status detection rates with CarrierSeq ECS Kit and ACMG supplemental panel covering 447 genes total with GS workflow for the analysis of >36,000 nonbenign CNVs, for SNVs, and for indels

Set standards in cytogenetics with the new CytoScan HD Accel Array
  • A two-day assay workflow
  • 50% less input sample required (100 ng)
  • Improved coverage in more than 5,000 genome regions
  • Expanded reference model for improved data quality even with challenging sample types
  • Reproducible and reliable results with minimal failure rate

The CytoScan Dx Assay is now IVDR-compliant

The CytoScan Dx Assay and Chromosome Analysis Suite (ChAS) Dx Software enable cytogenetics testing laboratories to adapt to the latest medical device safety and efficacy frameworks and conformity assessments for postnatal application.

The complete cytogenetics suite is a sample-to-insight solution that includes the CytoScan Dx Assay, a reagent kit, the GeneChip System 3000Dx platform for array processing, and user‑friendly ChAS Dx Software.

For Research Use Only. Not for use in diagnostic procedures.