Faculty, Staff and Student Publications

Authors

    Language

    English

    Publication Date

    1-22-2024

    Journal

    Briefings in Bioinformatics

    DOI

    10.1093/bib/bbae097

    PMID

    38493341

    PMCID

    PMC10944571

    PubMedCentral® Posted Date

    March 2024

    PubMedCentral® Full Text Version

    Post-print

    Abstract

    Kinase fusion genes are the most active fusion gene group in human cancer fusion genes. To help choose the clinically significant kinase so that the cancer patients that have fusion genes can be better diagnosed, we need a metric to infer the assessment of kinases in pan-cancer fusion genes rather than relying on the sample frequency expressed fusion genes. Most of all, multiple studies assessed human kinases as the drug targets using multiple types of genomic and clinical information, but none used the kinase fusion genes in their study. The assessment studies of kinase without kinase fusion gene events can miss the effect of one of the mechanisms that enhance the kinase function in cancer. To fill this gap, in this study, we suggest a novel way of assessing genes using a network propagation approach to infer how likely individual kinases influence the kinase fusion gene network composed of ~5K kinase fusion gene pairs. To select a better seed of propagation, we chose the top genes via dimensionality reduction like a principal component or latent layer information of six features of individual genes in pan-cancer fusion genes. Our approach may provide a novel way to assess of human kinases in cancer.

    Keywords

    kinase, fusion gene, gene assessment, network propagation, variational autoencoder, feature reduction

    Published Open-Access

    yes

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