CheckV assesses the quality and completeness of metagenome-assembled viral genomes.

Published on May 1, 2021in Nature Biotechnology36.558
· DOI :10.1038/S41587-020-00774-7
Stephen Nayfach18
Estimated H-index: 18
(LBNL: Lawrence Berkeley National Laboratory),
Antonio P. Camargo6
Estimated H-index: 6
(State University of Campinas)
+ 3 AuthorsNikos C. Kyrpides100
Estimated H-index: 100
(LBNL: Lawrence Berkeley National Laboratory)
Sources
Abstract
Millions of new viral sequences have been identified from metagenomes, but the quality and completeness of these sequences vary considerably. Here we present CheckV, an automated pipeline for identifying closed viral genomes, estimating the completeness of genome fragments and removing flanking host regions from integrated proviruses. CheckV estimates completeness by comparing sequences with a large database of complete viral genomes, including 76,262 identified from a systematic search of publicly available metagenomes, metatranscriptomes and metaviromes. After validation on mock datasets and comparison to existing methods, we applied CheckV to large and diverse collections of metagenome-assembled viral sequences, including IMG/VR and the Global Ocean Virome. This revealed 44,652 high-quality viral genomes (that is, >90% complete), although the vast majority of sequences were small fragments, which highlights the challenge of assembling viral genomes from short-read metagenomes. Additionally, we found that removal of host contamination substantially improved the accurate identification of auxiliary metabolic genes and interpretation of viral-encoded functions.
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