ViralCC retrieves complete viral genomes and virus-host pairs from metagenomic Hi-C data
ViralCC retrieves complete viral genomes and virus-host pairs from metagenomic Hi-C data
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London: Nature Publishing Group UK
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English
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London: Nature Publishing Group UK
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The introduction of high-throughput chromosome conformation capture (Hi-C) into metagenomics enables reconstructing high-quality metagenome-assembled genomes (MAGs) from microbial communities. Despite recent advances in recovering eukaryotic, bacterial, and archaeal genomes using Hi-C contact maps, few of Hi-C-based methods are designed to retrieve viral genomes. Here we introduce ViralCC, a publicly available tool to recover complete viral genomes and detect virus-host pairs using Hi-C data. Compared to other Hi-C-based methods, ViralCC leverages the virus-host proximity structure as a complementary information source for the Hi-C interactions. Using mock and real metagenomic Hi-C datasets from several different microbial ecosystems, including the human gut, cow fecal, and wastewater, we demonstrate that ViralCC outperforms existing Hi-C-based binning methods as well as state-of-the-art tools specifically dedicated to metagenomic viral binning. ViralCC can also reveal the taxonomic structure of viruses and virus-host pairs in microbial communities. When applied to a real wastewater metagenomic Hi-C dataset, ViralCC constructs a phage-host network, which is further validated using CRISPR spacer analyses. ViralCC is an open-source pipeline available at
https://github.com/dyxstat/ViralCC
.
Metagenomic Hi-C enables genome retrieval in microbial samples. Here, the authors develop an integrative method to recover complete viral genomes and detect virus-host pairs using metagenomic Hi-C data....
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ViralCC retrieves complete viral genomes and virus-host pairs from metagenomic Hi-C data
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TN_cdi_doaj_primary_oai_doaj_org_article_41e7addd345e4718be009f0d3d818400
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_41e7addd345e4718be009f0d3d818400
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2041-1723
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2041-1723
DOI
10.1038/s41467-023-35945-y