Mayo Clinic at AMP 2026

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

Mayo Clinic brings 12 presentations to AMP 2026 in Seattle. Its program centres on measurable residual disease testing in blood cancers, long-read sequencing and the informatics behind variant calling. It also covers DNA methylation and artificial intelligence for classifying central nervous system tumours, and weighs FISH against RNA sequencing for structural variants in solid tumours.

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

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