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Text-mining-based feature selection for anticancer drug response prediction. | LitMetric

Text-mining-based feature selection for anticancer drug response prediction.

Bioinform Adv

Department of Biochemistry, Microbiology & Immunology, University of Ottawa, Ottawa, K1H8M5, Canada.

Published: March 2024

AI Article Synopsis

  • Scientists are trying to predict how patients with cancer will respond to treatments by studying their genes, which is really important for personalized medicine.
  • They found that using special features from scientific papers (called text-mining) helps create better computer models for predicting treatment responses compared to traditional methods.
  • The study shows that text-mining is a simple and effective way to improve these models, and more info is available online if anyone wants to learn more.

Article Abstract

Motivation: Predicting anticancer treatment response from baseline genomic data is a critical obstacle in personalized medicine. Machine learning methods are commonly used for predicting drug response from gene expression data. In the process of constructing these machine learning models, one of the most significant challenges is identifying appropriate features among a massive number of genes.

Results: In this study, we utilize features (genes) extracted using the text-mining of scientific literatures. Using two independent cancer pharmacogenomic datasets, we demonstrate that text-mining-based features outperform traditional feature selection techniques in machine learning tasks. In addition, our analysis reveals that text-mining feature-based machine learning models trained on data also perform well when predicting the response of cancer models. Our results demonstrate that text-mining-based feature selection is an easy to implement approach that is suitable for building machine learning models for anticancer drug response prediction.

Availability And Implementation: https://github.com/merlab/text_features.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11009020PMC
http://dx.doi.org/10.1093/bioadv/vbae047DOI Listing

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