Diagnostics companies at AMP 2026

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

40 diagnostics companies are at AMP 2026 — 34 presentations on the program and 37 with a booth in the exhibit hall. Most represented: Roche Diagnostics (3 on the program), Guardant Health (2 on the program), Natera (2 on the program). 23 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 1–13 of 40 organizations
OrganizationAMP 2026 Attendance
Roche Diagnostics
Indianapolis, IN
DiagnosticsDiamond Partner
Clinical diagnostics, life science research, digital PCR and next-generation sequencing systems and assays for laboratories.
Booth
Exhibiting at Booth 700
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
🏅Diamond Partner
Workshop
Wed, Nov 11
10:00am–10:50am
Unlocking the Complete Lyo-Ready Workflow: From Sample Preparation to Amplification
A shelf-stable reagent set spanning sample prep, reverse transcription and amplification for assays built without cold-chain storage.
Workshop
Wed, Nov 11
11:00am–11:50am
Automated and Integrated Genomic Profiling of Hematologic Malignancies
Sequencing workflows for blood cancers that report mutations, structural variants and clonal evolution in one automated run.
Workshop
Wed, Nov 11
12:00pm–12:50pm
Next-Generation Sequencing with Roche’s AXELIOS 1 Platform
Roche's AXELIOS 1 sequencer and its expansion-based chemistry, covering accuracy, read length and run flexibility.
Workshop
Wed, Nov 11
1:00pm–1:50pm
Versatile Whole-exome Sequencing Enables End-to-end Phenotype-driven DNA-variant identification or RNA-fusion detection
Phenotype-driven exome workflows for germline variant discovery, plus two RNA-sequencing routes to fusions.
Workshop
Wed, Nov 11
9:00am–9:50am
Advancing HLA Class I Typing Through Comprehensive Genomic Profiling
Adding HLA class I typing to comprehensive genomic profiling, with immuno-oncology uses from checkpoint inhibitors to cell therapy.
Workshop hosted by Foundation Medicine
Guardant Health
Palo Alto, CA
Diagnostics
Precision oncology company offering blood and tissue tests, real-world data and AI analytics for cancer care.
Booth
Exhibiting at Booth 1043
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
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.
Workshop hosted by QIAGEN
Natera
San Carlos, CA
Diagnostics
Cell-free DNA testing company; Signatera is a custom ctDNA test for molecular residual disease assessment and treatment monitoring.
Booth
Exhibiting at Booth 445
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
4:00pm–4:50pm
Title: Advancements in MRD Testing: The Expanding Role of Digital Pathology and AI
Digital pathology and machine learning applied to specimen assessment and interpretation in residual disease testing.
Diagnostics
Molecular information company providing comprehensive genomic profiling to inform cancer treatment decisions.
Booth
Exhibiting at Booth 1701, MR14
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
8:00am–8:50am
Molecular Residual Disease in Breast Cancer: Advancing Surveillance and Clinical Decision-Making
Tissue-informed circulating tumor DNA testing in breast cancer, from baseline through surveillance and early recurrence detection.
Workshop
Wed, Nov 11
9:00am–9:50am
Advancing HLA Class I Typing Through Comprehensive Genomic Profiling
Adding HLA class I typing to comprehensive genomic profiling, with immuno-oncology uses from checkpoint inhibitors to cell therapy.
Talk
Thu, Nov 12
7:15am–8:15am
Adapting Communication Strategies for Today's Pathology Learners (A Special EdCoP Event)
Teaching pathology trainees across generations and learning styles, including feedback and handling performance problems.
Arima Genomics
Carlsbad, CA
Diagnostics
Cancer diagnostics from whole-genome sequence and structure; runs the CLIA-certified Aventa clinical lab and supplies research kits and informatics.
Booth
Exhibiting at Booth 536
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
2:00pm–2:50pm
Aventa Clinical Testing Powered by Arima Hi-C: Revealing Actionable Genomic Structure Across Lymphoma, Lung Cancer, and Sarcoma
Hi-C sequencing of FFPE tissue to map fusions and rearrangements in lymphoma, lung cancer and sarcoma cases.
Inocras
San Diego, CA
Diagnostics
Whole-genome sequencing and AI-driven bioinformatics for cancer and rare disease, offering clinical testing and research data integration.
Booth
Exhibiting at Booth 2305
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
MRC Holland
Amsterdam, Netherlands
Diagnostics
Assays for gene copy number and methylation detection, including MLPA and digitalMLPA probemixes for hereditary disorders and tumour profiling.
Booth
Exhibiting at Booth 643
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
1:00pm–1:50pm
Strategies for Optimizing Nucleic Acid Extraction in Molecular Oncology Workflows: Liquid Biopsy, FFPE, and Beyond
Magnetic bead extraction tuned for high-throughput oncology workflows, covering FFPE tissue and cell-free DNA from plasma.
Workshop hosted by Revvity
Diagnostics
CAP and CLIA certified laboratory offering cell-free DNA and RNA liquid biopsy testing for cancer.
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 hosted by QIAGEN
Diagnostics
Blood-cancer diagnostics company whose genome sequencing test on blood or bone marrow diagnoses and guides treatment of multiple myeloma.
Workshop
Wed, Nov 11
12:00pm–12:50pm
Next-Generation Sequencing with Roche’s AXELIOS 1 Platform
Roche's AXELIOS 1 sequencer and its expansion-based chemistry, covering accuracy, read length and run flexibility.
Workshop hosted by Roche Diagnostics
Univ8 Genomics
Belfast, UK
Diagnostics
Makes targeted NGS assays for leukaemia, lymphoma and myeloid cancers that detect clonality, translocations, copy number changes and mutations in one test.
Workshop
Wed, Nov 11
11:00am–11:50am
Automated and Integrated Genomic Profiling of Hematologic Malignancies
Sequencing workflows for blood cancers that report mutations, structural variants and clonal evolution in one automated run.
Workshop hosted by Roche Diagnostics
Diagnostics
Supplies clinical labs and assay developers with amplification-based enrichment and long-read sequencing products for genetic and oncology testing.
Booth
Exhibiting at Booth 737, 837
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
11:00am–11:50am
Deep Sensitivity Meets Workflow Efficiency: Optimizing HemOnc MRD Testing in Your Laboratory
Quantitative PCR for myeloid residual disease, including laboratory experience validating a new PML-RARA kit and its workflow.
Diagnostics
Next-generation sequencing kits for cancer testing built on SLIMamp and PiVAT technologies, in research-use and in vitro diagnostic formats.
Booth
Exhibiting at Booth 928, MR8
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm
Workshop
Wed, Nov 11
10:00am–10:50am
Rapid NGS That Scales: Clinical Implementation of oncoReveal® Myeloid NGS on the MiSeq i100
Bringing a myeloid sequencing panel in house on a benchtop sequencer, reaching roughly three-day turnaround across 200 samples.
Workshop
Wed, Nov 11
8:00am–8:50am
Evaluation and Analytical Validation of a Rapid NGS Panel to Evaluate Lymphoid Malignancies
Validating a rapid sequencing panel for lymphoid cancers, with wider gene coverage and shorter turnaround in a hospital lab.
Workshop
Wed, Nov 11
9:00am–9:50am
Bringing Liquid Biopsy Closer to Patients: Rapid Local NGS Testing for Biomarker Assessment in Advanced Breast Cancer
Running ctDNA testing locally for advanced breast cancer cuts turnaround, raising questions of validation, interpretation and quality control.
Diagnostics
qPCR and digital PCR assays for oncology and pharmacogenetics research, covering mutation detection, gene expression and genetic variants, using Clickmers aptamer technology.
Booth
Exhibiting at Booth 2302
Thu, Nov 1211:15am–7:00pmFri, Nov 139:00am–4:00pmSat, Nov 149:00am–1:30pm

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