Instrument and reagent vendors at AMP 2026

Nov 10–14, 2026 Seattle, WA ~2k attendees Website

109 instrument and reagent vendors are at AMP 2026 — 66 presentations on the program and 104 with a booth in the exhibit hall. Most represented: PacBio (3 on the program), Promega (3 on the program), Bio-Rad Laboratories (2 on the program). 37 of them have their own page in this guide. As of Sep 25, 2026.

All 298 organizations at AMP 2026 →

Program track
Top represented
Showing 1–10 of 109 organizations
OrganizationAMP 2026 Attendance
PacBio
Menlo Park, CA
Suppliers
Sequencing technologies combining long reads with high accuracy for genomes, transcriptomes and epigenomes.
Booth
Exhibiting at Booth 1018
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
9:00am–9:50am
Full Stack Somatic: Connecting Long-Read HiFi WGS to Clinical Genomic Reporting
A containerized somatic long-read whole-genome pipeline running from raw data through variant interpretation to a clinical report.
Workshop hosted by GenomOncology
Workshop
Fri, Nov 13
12:00pm–12:30pm
Accelerating Clinical Genomics with HiFi Sequencing: Targeted and Rapid Whole-Genome Workflows
Long-read workflows for repeat expansion disorders and other hard genomic regions, plus a faster whole-genome protocol.
Promega
Madison, WI
Suppliers
Nucleic acid extraction, PCR reagents and custom or OEM manufacturing for clinical laboratories, with technical support.
Booth
Exhibiting at Booth 610
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
8:00am–8:50am
From Hands-On to Hands-Off: Automating FFPE, Blood, and Bone Marrow Extraction on the Clear Dx System
Automated nucleic acid extraction from FFPE, blood and bone marrow, with yield reproducibility, contamination checks and time saved.
Workshop
Wed, Nov 11
9:00am–9:50am
OncoMate® MSI Dx as a Companion Diagnostic for Microsatellite Instability: Clinical Context, Validation, and Performance
Microsatellite instability testing as a companion diagnostic for checkpoint inhibitor eligibility, with accuracy and concordance data.
Suppliers
Products for life science research and clinical diagnostics, including droplet digital PCR, real-time PCR and molecular quality controls and standards.
Booth
Exhibiting at Booth 537, MR16
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
8:00am–8:50am
MRD Detection & Monitoring in Solid Tumors and Heme Malignancies Using Personalized Tumor Informed Droplet Digital PCR (ddPCR) Assays in Research Settings
Tumour-informed droplet digital PCR assays for tracking residual disease in both blood cancers and solid tumours.
Workshop
Thu, Nov 12
6:15pm–6:45pm
Unlocking More from Every Sample: New Multiplex Oncology Assays and Emerging MRD Applications with the QX700™ ddPCR™ System
Multiplexed droplet digital PCR assays that pull more oncology biomarker data from limited samples, including residual disease monitoring.
Cellecta
Mountain View, CA
Suppliers
Genomic products and services for drug target and biomarker discovery: viral vector production, functional screening, cell engineering and multiplex qRT-PCR.
Booth
Exhibiting at Booth 2205
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
2:00pm–2:50pm
From Repertoire to Response: A Workflow for Mapping Antigen-Specific T- and B-Cell Clonotypes for Receptor-Based Target Discovery
Pairing immune receptor sequencing with antigen screening to rank tumour-specific T- and B-cell clonotypes, including from plasma.
Workshop
Sat, Nov 14
9:30am–10:00am
Discovery and Validation of T- and B-Cell Clonotypes to Drive Next-Level Drug and Biomarker Discovery
An end-to-end route from bulk and single-cell receptor sequencing to screening that surfaces drug and biomarker candidates.
Countable Labs
Palo Alto, CA
Suppliers
Countable PCR uses single-molecule isolation for fusion and rare variant detection, minimal residual disease monitoring and absolute ctDNA quantification.
Booth
Exhibiting at Booth 943
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
12:00pm–12:50pm
A New Detection Paradigm for Heme Oncology: High-Color Single-Molecule PCR for Reproducible MRD and Monitoring
Single-molecule PCR across millions of partitions to count BCR::ABL1, KMT2A and other blood cancer variants reproducibly.
Covaris
Woburn, MA
Suppliers
Sample preparation for multiomics research and clinical labs, using focused-acoustics instruments, consumables, reagents and kits. A PerkinElmer company.
Booth
Exhibiting at Booth 2409
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
3:00pm–3:50pm
Optimizing FFPE tissue stewardship: Covaris truXTRAC automated workflow delivers superior performance for tumor-informed Haystack® MRD assay
Getting more DNA and RNA from each FFPE slide so scarce tumour tissue stretches across several sequencing assays.
Workshop
Thu, Nov 12
3:45pm–4:15pm
Optimized Automated Extraction for FFPE Tissue Cores
Automated simultaneous DNA and RNA extraction from FFPE cores and sections, validated for sequencing-grade yield.
Illumina
San Diego, CA
SuppliersGold Partner
Sequencing instruments and reagents for clinical, research and applied markets, spanning oncology, reproductive health and genetic disease.
Booth
Exhibiting at Booth 727, MR1, MR2
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
🏅Gold Partner
Workshop
Wed, Nov 11
11:00am–11:50am
Expanding Precision Oncology: Practical Strategies for Integrating Tissue and Liquid Biopsy Comprehensive Genomic Profiling
Tissue and liquid biopsy genomic profiling run side by side, covering test algorithms, lab operations and case examples.
Workshop
Wed, Nov 11
12:00pm–12:50pm
Genome as a Platform: Advancing MRD Research with Illumina Whole Genome Sequencing Oncology Prep
Whole-genome sequencing as a single platform for molecular residual disease research, with early analytical performance data.
Workshop
Wed, Nov 11
2:00pm–2:50pm
Unlocking AML Biology with 5-Base Whole-Genome Sequencing: Integrated Genomic and Epigenomic Profiling for Biomarker Discovery
Five-base whole-genome sequencing reads methylation and genomic variation from one AML sample to find research biomarkers.
Workshop
Fri, Nov 13
3:00pm–3:30pm
Comprehensive Tumor Profiling Beyond Panels: Methylation-Aware WGS Enabled by Advanced Informatics
Whole-genome sequencing with methylation and fragmentomic analysis moves tumor profiling beyond targeted panels, using DRAGEN informatics.
SuppliersSilver Partner
Research and diagnostic solutions for molecular laboratories: next-generation sequencing, real-time PCR, Sanger sequencing and bioinformatics across oncology, pharmacogenomics and infectious disease.
Booth
Exhibiting at Booth 709, MR10, MR4
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
🏅Silver Partner
Workshop
Wed, Nov 11
10:00am–10:50am
Beyond Tissue: Implementing Alternative Analytes for Molecular Diagnostics in Clinical Practice
Using cerebrospinal fluid and fine needle aspirate supernatant for sequencing when tumour tissue is scarce or unavailable.
Workshop
Wed, Nov 11
11:00am–11:50am
Novel NGS Applications in Oncology Research: TCR Sequencing and Methylation-Based ctDNA Analysis
T-cell receptor sequencing and methylation-based circulating tumor DNA analysis open new angles on immune response and tumor signals.
Workshop
Wed, Nov 11
1:00pm–1:50pm
Implementing Clinical Pharmacogenomics: Practical Lessons from Assay to Actionable Care
Getting pharmacogenomic testing into routine care: test selection, lab workflow, reporting, reimbursement and health record integration.
Workshop
Wed, Nov 11
2:00pm–2:50pm
Advancing precision oncology research: Integrating pharmacogenomics and genomic profiling using a single, rapid NGS workflow on the Genexus System
Folding DPYD pharmacogenomic content into tumour sequencing so one run covers both drug-response and tumour profiling.
Workshop
Wed, Nov 11
3:00pm–3:50pm
Bridging the Clinical Gap: Retrospective Microsatellite Instability Testing to Inform Complex Biospecimen Cohort Generation
Microsatellite instability testing across hundreds of banked tumor specimens builds characterized cohorts for immunotherapy research.
Workshop
Wed, Nov 11
8:00am–8:50am
The Precision Pathway: How Pathologists Are Transforming Biomarker Discovery, Selection, and Clinical Impact Across GU Cancers
Biomarker selection, specimen handling and reporting for genitourinary cancers, worked through interactive case discussions.
Workshop
Wed, Nov 11
9:00am–9:50am
From Assay to Answer: Genomic Technologies and Multiplex Workflow Solutions for Infectious Disease Research
Pathogen detection by qPCR and digital PCR, with assay design and multiplexing choices for adding targets within one reaction.
Workshop
Thu, Nov 12
4:25pm–4:55pm
It's Hard to Treat What You Can't See: Leveraging Molecular Diagnostics to Improve Care of Patients with Pancreatic Lesions
Pancreatic lesions are hard to call on imaging and cytology alone; molecular testing can sharpen diagnosis and risk stratification.
Workshop
Thu, Nov 12
6:15pm–6:45pm
Unlocking New Possibilities in Myeloid Malignancies MRD Assessment with NGS
An NGS assay for measurable residual disease in myeloid cancers, covering its gene content, workflow and reported performance.
LGC
Teddington, UK
Suppliers
Quality controls, reference materials, diagnostic panels, NGS controls and proficiency testing for clinical laboratories, through its SeraCare clinical diagnostics business.
Booth
Exhibiting at Booth 1804, MR13
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
12:00pm–12:50pm
You’re So Naïve: Best Practices and Gold-Standard Reference Material for Tumor-Agnostic MRD Testing
Tumor-agnostic residual disease assays face validation hurdles, weighed against tumor-informed testing alongside reference materials.
QIAGEN
Venlo, Netherlands
Suppliers
Sample preparation kits, assay technologies and bioinformatics for extracting DNA and RNA insights in research, clinical and applied testing laboratories.
Booth
Exhibiting at Booth 529, MR18
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
1:00pm–1:50pm
Advancing Cell-Free Nucleic Acid Testing: Integrated Workflows for Prenatal and Oncology Applications
Cell-free DNA and RNA workflows for prenatal screening and oncology, including why DNA-only sequencing misses actionable fusions.
Workshop
Wed, Nov 11
2:00pm–2:50pm
Building Scalable Clinical Genomics Workflows: Practical Lessons from Leading Laboratories
Scaling sequencing operations in molecular labs, plus how to keep trust in AI-assisted variant interpretation.

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Not affiliated with the Association for Molecular Pathology. Organization details are derived from AMP’s published lists. Submit a correction