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1
Introduction
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Welcome
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Background
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Example
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General workflow
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Can we train accurate diagnostic or problem prognostic models
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The same label assumption
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Multiple instance learning
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Data efficiency
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Recap
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Framework
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Segmentation
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Embedding
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Attention pooling
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Summary
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Benchmarks
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Attention scores
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Cell phone microscopy
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Results
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Summarize
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Code
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Prognosis
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Primary origins of ceps
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Study design
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Classification
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Heatmaps
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Interactive demo
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Attention heating map
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Dummy tool
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High certainty diagnosis
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Differential diagnosis
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Thank you
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Which regions in the slide will contribute
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Can the primary originate from one single primary
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Is the morphology more nuanced
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Clustering
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Outro
Description:
Explore a comprehensive framework for developing interpretable diagnostic and prognostic machine learning models using digitized histopathology slides in this 52-minute conference talk by Max Lu from Stanford University. Learn about a scalable method that doesn't require manual annotation of regions of interest and can be applied to tens of thousands of samples. Discover applications ranging from cancer subtyping and prognosis to predicting primary origins of metastatic tumors. Gain insights into weakly-supervised, large-scale computational pathology techniques, including multiple instance learning, attention pooling, and data efficiency. Examine benchmarks, attention scores, and interactive demos showcasing the framework's capabilities in cell phone microscopy, prognosis, and primary origin prediction of metastatic tumors.

Weakly-Supervised, Large-Scale Computational Pathology for Diagnosis and Prognosis - Max Lu

Stanford University
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