Hematopathology at AMP 2026

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

15 organizations at AMP 2026 present work in hematopathology: 14 academic medical centres, children's hospitals and universities and 1 public organization. Between them they bring 71 presentations to the program. Most represented: Mayo Clinic (11 on the program), MD Anderson Cancer Center (9 on the program), Palmetto GBA (8 on the program). 15 of them have their own page in this guide. As of Sep 25, 2026.

All 298 organizations at AMP 2026 →

Format
Top represented
Showing 1–5 of 15 organizations
OrganizationAMP 2026 Attendance
Mayo Clinic
Rochester, MN
Med centres
Academic medical center and health system whose laboratories develop and run clinical molecular and genomic testing.
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 hosted by Illumina
Talk
Sat, Nov 14
10:15am–10:45am
FISH vs. RNA sequencing for Structural Variant Detection in Solid Tumors: Strengths and Limitations
Case-based comparison of break-apart FISH and RNA sequencing for finding gene rearrangements in solid tumors, including FFPE pitfalls.
Hematopathology · Lab Management · Solid Tumors
Session
Sat, Nov 14
10:15am–11:45am
Talk
Sat, Nov 14
2:30pm–3:00pm
CNVpytor: Comprehensive Detection, Annotation, and Visualization of Germline and Somatic Copy Number Variations
CNVpytor, a tool combining read depth and B-allele frequency to call and visualize germline and somatic copy number changes.
Informatics
Med centres
Comprehensive cancer center and academic medical institution in Houston, with clinical molecular diagnostics laboratories.
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 hosted by Thermo Fisher Scientific
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.
Workshop hosted by Countable Labs
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 hosted by Illumina
Workshop
Thu, Nov 12
12:00pm–12:30pm
AMP Practice Guidelines Meet the Authors Series: Lung Guideline Update
New lung cancer molecular testing recommendations from the updated joint practice guideline, with the evidence and process behind them.
Session
Fri, Nov 13
10:15am–11:45am
Workshop
Fri, Nov 13
9:30am–10:00am
Electronic Genome Mapping for Structural Variant Detection: Implications for Advancing Clinical Research in Heme Malignancies
Electronic genome mapping weighed against karyotyping, FISH and optical mapping for structural variants, including marrow versus blood samples.
Workshop hosted by Nabsys
Talk
Sat, Nov 14
10:15am–11:00am
From AI Promise to Clinical Practice: Which Genomic Foundation Models Can You Trust in Molecular Testing?
How well DNA foundation models actually perform on clinical genomic tasks, and how to judge which ones to trust.
Informatics
Talk
Sat, Nov 14
3:00pm–3:30pm
Direct DNA Methylation Analysis by Single Molecule Real-Time Sequencing
A transformer model reads polymerase kinetics from SMRT sequencing to call 5mC, 5hmC and 6mA base modifications directly.
Technical Topics
Palmetto GBA
Columbia, SC
Gov/NGO
Medicare Administrative Contractor that runs the MolDX program, setting coverage and reimbursement policy for molecular diagnostic tests.
Session
Thu, Nov 12
10:15am–11:45am
Session
Fri, Nov 13
3:45pm–4:45pm
Technical Topics Plenary Session
Technical Topics
  1. 3:45pm–4:45pmStepping Towards Single-Molecule Protein Sequencing Using NanoporesUniversity of Washington
Med centres
Public research university and academic medical centre in Ann Arbor with clinical cancer genomics and molecular diagnostics programmes.
Session
Thu, Nov 12
10:15am–11:45am
Talk
Thu, Nov 12
11:00am–11:45am
Molecular-Resolution Spatial Inference of Subcellular Transcriptional Programs
Submicron spatial transcriptomics plus segmentation-free analysis that assigns cell type and transcriptional programs from individual transcripts.
Technical Topics
Workshop
Thu, Nov 12
12:40pm–1:10pm
AI in Trainee Education: A Demonstration and Discussion
Building a large language model study aid for pathology trainees, alongside survey findings on how trainees and educators use AI.
Talk
Thu, Nov 12
8:30am–8:45am
Opening Remarks
  1. 8:30am–8:45amOpening Remarks
Talk
Fri, Nov 13
2:00pm–2:45pm
Development and Use of Menin Inhibitors as Precision Medicines for Acute Myeloid Leukemia
Development of menin inhibitors for KMT2A-rearranged and NPM1-mutant acute myeloid leukemia, plus response biomarkers and resistance.
Hematopathology
Med centres
Cancer hospital and research institute in New York with a large clinical tumour sequencing and molecular diagnostics programme.
Session
Thu, Nov 12
1:15pm–2:15pm
Talk
Thu, Nov 12
2:30pm–3:00pm
AMP Clinical Validation of cfDNA and ctDNA Assays Working Group
Setting validation standards for liquid biopsy assays in oncology, with attendee input shaping the guideline under development.
Talk
Thu, Nov 12
3:00pm–3:30pm
AMP Copy Number Alterations Working Group
Copy number alterations called from sequencing: how those assays are validated, reported and read next to FISH, cytogenetics and microarray.
Workshop
Thu, Nov 12
4:25pm–4:55pm
Want to get involved with AMP?
Volunteering pathways in the professional society, from short time-limited tasks through committee membership and leadership roles.
Session
Fri, Nov 13
10:15am–11:45am
Talk
Fri, Nov 13
11:15am–11:45am
AlphaMissense for Identifying Pathogenic Missense Mutations in DNA Damage Repair Genes in Cancer
Using AlphaMissense and related AI tools to flag pathogenic missense variants in DNA damage repair genes in cancer.
Genetics
Talk
Fri, Nov 13
1:15pm–2:45pm
Data Analysis, Interpretation, and Discovery in 100,000 Patients With Cancer
Combining somatic, germline and clinical data from over 100,000 cancer patients to support variant interpretation, trials and discovery.
Informatics
Session
Sat, Nov 14
10:15am–11:45am
Update on the Role of CtDNA-Based Detection of MRD in Clinical Trials and Beyond for Solid Tumors
Solid Tumors
  1. 10:15am–11:00amMinimal Residual Disease in Colorectal Cancer: Opportunities for therapeutic developmentThe University of Texas MD Anderson Cancer Center, Houston, TX
  2. 11:00am–11:45amLiquid Biopsy Biomarkers for Early Detection of Treatment Response and Disease MonitoringMCGill University, Research Institute of the McGill University Health Centre

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