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10.1093/nargab/lqab004

http://scihub22266oqcxt.onion/10.1093/nargab/lqab004
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33554119!7849996!33554119
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suck abstract from ncbi


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pmid33554119      NAR+Genom+Bioinform 2021 ; 3 (1): lqab004
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  • Interpretable detection of novel human viruses from genome sequencing data #MMPMID33554119
  • Bartoszewicz JM; Seidel A; Renard BY
  • NAR Genom Bioinform 2021[Mar]; 3 (1): lqab004 PMID33554119show ga
  • Viruses evolve extremely quickly, so reliable methods for viral host prediction are necessary to safeguard biosecurity and biosafety alike. Novel human-infecting viruses are difficult to detect with standard bioinformatics workflows. Here, we predict whether a virus can infect humans directly from next-generation sequencing reads. We show that deep neural architectures significantly outperform both shallow machine learning and standard, homology-based algorithms, cutting the error rates in half and generalizing to taxonomic units distant from those presented during training. Further, we develop a suite of interpretability tools and show that it can be applied also to other models beyond the host prediction task. We propose a new approach for convolutional filter visualization to disentangle the information content of each nucleotide from its contribution to the final classification decision. Nucleotide-resolution maps of the learned associations between pathogen genomes and the infectious phenotype can be used to detect regions of interest in novel agents, for example, the SARS-CoV-2 coronavirus, unknown before it caused a COVID-19 pandemic in 2020. All methods presented here are implemented as easy-to-install packages not only enabling analysis of NGS datasets without requiring any deep learning skills, but also allowing advanced users to easily train and explain new models for genomics.
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