Stanford University at AMP 2026

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

Stanford University brings 9 presentations to AMP 2026 in Seattle. Its sessions cover cell-free DNA and liquid biopsy, mutational signatures and gene fusions in solid tumours, and metagenomic sequencing for infectious disease. One example is real-world institutional experience with MassARRAY-based UBA1 testing for VEXAS syndrome.

OrganizationAMP 2026 Attendance
Med centres
Private research university in California whose medical school runs clinical genomics, molecular pathology and metagenomic sequencing laboratories.
Session
Thu, Nov 12
10:15am–11:45am
Talk
Thu, Nov 12
11:00am–11:45am
Multi-Omic Single Molecule Profiling of Cell Free DNA Reveals Cancer Signatures
Single-molecule reads of scant cell-free DNA capture methylation, hydroxymethylation and fragmentation to profile cancers and spot brain metastases.
Informatics
Workshop
Fri, Nov 13
3:00pm–3:30pm
The Practice Pulse: Identifying Where Members Need AMP Most (An AMP Clinical Practice Committee Open Forum)
Where clinical practice gaps sit today, with member input steering which problems the committee takes on next.
Session
Sat, Nov 14
1:45pm–2:15pm
AMP Electronic Health Record (EHR) Interoperability for Clinical Genomics Data Working Group
A working-group update on making genomic variant data interoperable in electronic health records, and where standards still fall short.
Talk
Sat, Nov 14
2:45pm–4:00pm
Toward a Paradigm Shift in Personalized Therapies for Lymphoma Using Liquid Biopsies
Circulating tumor DNA in diffuse large B-cell lymphoma for genotyping, early response measurement and residual-disease-guided treatment.
Hematopathology · Technical Topics

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