Evidence map›Paper›PMID 35602188›Full record

ArticleCommunications medicine2021

A BERT model generates diagnostically relevant semantic embeddings from pathology synopses with active learning.

Youqing Mu, Hamid R Tizhoosh, Rohollah Moosavi Tayebi, Catherine Ross, Monalisa Sur, Brian Leber, Clinton J V Campbell

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Article in Communications medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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  8. Applications of Large Language Models in Pathology.Bioengineering (Basel, Switzerland) · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Youqing MuMcMaster University, Hamilton, ON Canada.ORCID 0000-0002-4561-5514
Hamid R TizhooshKimia Lab, University of Waterloo, Waterloo, ON Canada.ORCID 0000-0001-5488-601X
Rohollah Moosavi TayebiMcMaster University, Hamilton, ON Canada.
Catherine RossMcMaster University, Hamilton, ON Canada.
Monalisa SurMcMaster University, Hamilton, ON Canada.
Brian LeberMcMaster University, Hamilton, ON Canada.
Clinton J V CampbellMcMaster University, Hamilton, ON Canada.ORCID 0000-0002-8896-1134

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pathology synopses consist of semi-structured or unstructured text summarizing visual information by observing human tissue. Experts write and interpret these synopses with high domain-specific knowledge to extract tissue semantics and formulate a diagnosis in the context of ancillary testing and clinical information. The limited number of specialists available to interpret pathology synopses restricts the utility of the inherent information. Deep learning offers a tool for information extraction and automatic feature generation from complex datasets. Methods: Using an active learning approach, we developed a set of semantic labels for bone marrow aspirate pathology synopses. We then trained a transformer-based deep-learning model to map these synopses to one or more semantic labels, and extracted learned embeddings (i.e., meaningful attributes) from the model's hidden layer. Results: Here we demonstrate that with a small amount of training data, a transformer-based natural language model can extract embeddings from pathology synopses that capture diagnostically relevant information. On average, these embeddings can be used to generate semantic labels mapping patients to probable diagnostic groups with a micro-average F1 score of 0.779 Â ± 0.025. Conclusions: We provide a generalizable deep learning model and approach to unlock the semantic information inherent in pathology synopses toward improved diagnostics, biodiscovery and AI-assisted computational pathology.

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Haematological cancerPathology

Identifiers

PMID35602188
PMCPMC9053264

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.