AI Article Synopsis

  • Liquid biopsies provide a less invasive way to diagnose and monitor cancer, using RNA sequencing data from tumor-educated platelets (TEPs).
  • The study involved analyzing a large dataset of over a thousand donors, employing machine learning techniques like convolutional neural networks and boosting algorithms to classify cancer presence with impressive accuracy.
  • Results indicate that TEP data can effectively distinguish between cancerous and non-cancerous patients, demonstrating significant potential for advancing cancer diagnostics without losing model performance across different hospital data.

Article Abstract

Liquid biopsies offer minimally invasive diagnosis and monitoring of cancer disease. This biosource is often analyzed using sequencing, which generates highly complex data that can be used using machine learning tools. Nevertheless, validating the clinical applications of such methods is challenging. It requires: (a) using data from many patients; (b) verifying potential bias concerning sample collection; and (c) adding interpretability to the model. In this work, we have used RNA sequencing data of tumor-educated platelets (TEPs) and performed a binary classification (cancer vs. no-cancer). First, we compiled a large-scale dataset with more than a thousand donors. Further, we used different convolutional neural networks (CNNs) and boosting methods to evaluate the classifier performance. We have obtained an impressive result of 0.96 area under the curve. We then identified different clusters of splice variants using expert knowledge from the Kyoto Encyclopedia of Genes and Genomes (KEGG). Employing boosting algorithms, we identified the features with the highest predictive power. Finally, we tested the robustness of the models using test data from novel hospitals. Notably, we did not observe any decrease in model performance. Our work proves the great potential of using TEP data for cancer patient classification and opens the avenue for profound cancer diagnostics.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10136732PMC
http://dx.doi.org/10.3390/cancers15082336DOI Listing

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