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, based on computationally quantified leukemic cell populations and limited clinical data, both readily available at diagnosis. We used explainable artificial intelligence (AI) to identify the key clinical characteristics and leukemic cell populations important for our ML models when making these predictions. Our findings highlight the importance of developing objective computational pipelines integrating immunophenotypic and genetic information in the risk stratification of AML.
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Artuur Couckuyt
Sofie Van Gassen
Annelies Emmaneel
Cytometry Part B Clinical Cytometry
Ghent University
Ghent University Hospital
VIB-UGent Center for Inflammation Research
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Couckuyt et al. (Thu,) studied this question.
www.synapsesocial.com/papers/69fff809f9353b931b7743ca — DOI: https://doi.org/10.1002/cyto.b.22230