ExoShorkie: predicting RNA-seq coverage of exogenous genomes in yeast by transfer learning.
basic_science · Level V
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- Record sourced from PubMed, PMID 42635208.
- Also identified by DOI 10.1093/bioinformatics/btag369.
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Abstract
Predicting the RNA-seq coverage of native and exogenous sequences is central to many molecular- and synthetic-biology applications. Substantial progress has been made in developing methods to predict the RNA-seq coverage of native genomic sequences, with the recently developed Shorkie achieving state-of-the-art performance in yeast. However, prediction performance of these methods over exogenous DNA is still unknown. Recent studies measured RNA-seq coverage of large exogenous genomes in yeast, providing a unique opportunity to train machine-learning models on a large exogenous sequence space and to improve both prediction performance and our understanding of regulatory mechanisms. We introduce ExoShorkie, a method we developed by extending Shorkie through transfer learning across multiple exogenous RNA-seq datasets. We demonstrate that ExoShorkie significantly improves prediction performance on held-out exogenous genomes and outperforms both a native-genome-trained Shorkie baseline and Yorzoi, the only competing method for predicting exogenous RNA-seq coverage in yeast, in cross-validation and in leave-one-genome-out evaluations. Furthermore, through interpretability analyses we reveal biologically meaningful regulatory motifs and distinct regulatory rules in exogenous genomes in yeast, providing new insights into transcriptional regulation. ExoShorkie is available at https://github.com/OrensteinLab/ExoShorkie.
Medical subject headings
- Genome, Fungal
- Saccharomyces cerevisiae
- RNA-Seq
- Software
- Genomics
- Sequence Analysis, RNA