ArticleBioinformatics (Oxford, England)2024
CrossIsoFun: predicting isoform functions using the integration of multi-omics data.
Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- DeepISO: deep learning-powered prediction of protein-protein interaction rewiring generated by alternative splicing.Genome biology · 2026Article
- ProteoformDB: an integrative database for functional roles of proteoforms.Database : the journal of biological databases and curation · 2026Article
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3 authors.
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Abstract
motivationIsoforms spliced from the same gene may carry distinct biological functions. Therefore, annotating functions at the isoform level provides valuable insights into the functional diversity of genomes. Since experimental approaches for determining isoform functions are time- and cost-demanding, computational methods have been proposed. In this case, multi-omics data integration helps enhance the model performance, providing complementary insights for isoform functions. However, current methods underperform in leveraging diverse omics data, primarily due to the limited power to integrate the heterogeneous feature domains. Besides, among the multi-omics data, isoform-isoform interactions (IIIs) are a key data source, as isoforms interact with each other to perform functions. Unfortunately, IIIs remain largely underutilized in isoform function predictions until now.
resultsWe introduce CrossIsoFun, a multi-omics data analysis framework for isoform function prediction. CrossIsoFun combines omics-specific and cross-omics learning for data integration and function prediction. In detail, CrossIsoFun uses a graph convolutional network (GCN) as the omics-specific classifier for each data source. The initial label predictions from GCNs are forwarded to the View Correlation Discovery Network (VCDN) and processed as a cross-omics integrative representation. The representation is then used to produce final predictions of isoform functions. In addition, an antoencoder within a cycle-consistency generative adversarial network (cycleGAN) is designed to generate IIIs from PPIs and thereby enrich the interactomics data. Our method outperforms the state-of-the-art methods on three tissue-naive datasets and 15 tissue-specific datasets with mRNA expression, sequence, and PPI data. The prediction of CrossIsoFun is further validated by its consistency with subcellular localization and isoform-level annotations with literature support. AVAILABILITY AND IMPLEMENTATION: CrossIsoFun is freely available at https://github.com/genemine/CrossIsoFun.
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