Association for Molecular Pathology Annual Meeting and Expo
Join Integrated DNA Technologies (IDT) at the Association for Molecular Pathology 2026 Annual Meeting & Expo in Seattle. Visit booth 1014 to explore customizable NGS solutions for cancer genomics and molecular pathology research, including flexible approaches for solid tumor profiling, blood cancer research, liquid biopsy, whole exome sequencing, and hybridization capture.
Whether you are building a new assay, scaling an existing workflow, or evaluating automation, our scientists can help you identify an approach that fits your sample types, throughput requirements, and research goals. Discover how our xGen™ and Archer™ portfolios support workflows from library preparation and target enrichment through analysis.
Bring your current assay or workflow challenge to booth 1014 and talk with our trusted experts about customization, workflow integration, and technical support.
Corporate Workshop
Title: Enabling scalable molecular profiling in cancer research: Automated hematologic malignancy workflows and emerging hybrid capture applications
Date & Time: November 11, 2026 @ 11:00 a.m. – 11:50 a.m. PST
Location: Chelan 5, Level 2, Arch at 800 Pike
Presented by:
Somak Roy, MD, Cincinnati Children’s Hospital
Randy Pares, MS, Integrated DNA Technologies
https://amp26.amp.org/corporate-workshops/attend-a-corporate-workshop/
Posters
| Title | Presenting Author | Day/Time | Info |
|---|---|---|---|
|
Archer VariantPlex™ copy number variation detection and visualization enables exon-level resolution without a panel of normals |
Brianna Fernandez |
Friday, November 13, 9:15-10:15 a.m. PST |
Poster Number: I036 Category: Informatics |
|
Uniform exome coverage enables high-quality germline variant detection across low‑GC and biologically relevant regions |
Mathew McNeill |
Saturday, November 14, 9:15-10:15 a.m. PST |
Poster Number: G023 Category: Genetics |
|
A deep learning design tool for automated probe optimization and coverage prediction in the xGen NGS hybridization capture workflow |
Jing Li |
Saturday, November 14, 9:15-10:15 a.m. PST |
Poster Number: I039 Category: Informatics |
Customer appreciation event
Thursday, Nov 12, 6:30-10:30 p.m. PST
Ask us at booth 1014 or contact your sales representative for details about our exclusive customer event with drinks, appetizers, and opportunities to connect with trusted experts.
Featured products
Explore cancer research solutions
Discover customizable, high-performing NGS solutions designed to support research across solid tumors, liquid biopsy, and MRD, and blood cancers. IDT offers flexible approaches spanning targeted sequencing, comprehensive genomic profiling, and broader genomic analysis to enable labs to overcome their evolving cancer research challenges.
Generate comprehensive insights for solid tumor research
Explore Archer NGS assay solutions designed to address solid tumor research challenges, including low-input and degraded samples, complex genomic alterations, workflow demands, and bioinformatics. Choose from targeted panels through comprehensive genomic profiling approaches, with FUSIONPlex™ and VARIANTPlex assays supporting detection of relevant DNA and RNA based alterations.
Advance blood cancer profiling
Explore Archer NGS assay solutions for blood cancer research, with predesigned panels supporting DNA- and RNA-based profiling across myeloid and other hematologic malignancies. FUSIONPlex, VARIANTPlex, and IMMUNOVerse™ solutions support research into alterations including fusions, SNVs, indels, ITDs, CNVs, expression, clonality, and MRD.
Connect assay design, workflow, and analysis
Archer NGS assay solutions combine Anchored Multiplex PCR (AMP™) chemistry with streamlined workflows and Archer Analysis, a software platform offering purpose-built bioinformatics, to support detection and analysis of genomic alterations. Assay options accommodate different sample volumes, from automated, high-throughput labs and lower-throughput manual workflows.
Connect with IDT and Beckman Coulter Life Sciences
Visit the IDT booth 1014 and/or Beckman Coulter Life Sciences booth 2301 to learn how complementary assay and automation capabilities can support more connected molecular workflows.
Streamline workflows for cfDNA and FFPE samples
Explore library preparation and workflow options developed for challenging inputs, including the xGen NGS cfDNA & FFPE Workflow Base Kit and xGen cfDNA and FFPE Library Prep Kit.
- Explore the xGen NGS cfDNA and FFPE Workflow Base Kit
- Explore the xGen cfDNA & FFPE Library Prep Kit
Expand exome research coverage
Learn how the xGen Exome Hyb Panel v2 and complementary spike-in content can support high-quality exome research across challenging and biologically relevant regions.
Build faster, more flexible hybrid capture workflows
Discover xGen Hybridization and Wash v3 reagents and talk with our specialists about workflows for limited-input samples and emerging hybrid capture applications.
Customize panels around your research
Develop custom hybridization capture content for your targets, applications, and performance requirements, with design support available for complex projects.