Abstract
AbstractImprovements in the accuracy and availability of long-read sequencing mean that complete bacterial genomes are now routinely reconstructed using hybrid (i.e. short- and long-reads) assembly approaches. Complete genomes allow a deeper understanding of bacterial evolution and genomic variation beyond small nucleotide variants (SNVs). They are also crucial for identifying plasmids, which often carry medically significant antimicrobial resistance (AMR) genes. However, small plasmids are often missed or misassembled by long-read assembly algorithms. Here, we present Hybracter, method for fast, automatic and scalable recovery of near-perfect complete bacterial genomes using a long-read first assembly approach. We compared Hybracter to existing automated hybrid assembly tools using a diverse panel of samples with manually curated ground truth reference genomes. We demonstrate that Hybracter is more accurate and faster than the existing gold standard automated hybrid assembler Unicycler. We also show that Hybracter with long-reads only is comparable to hybrid methods in recovering small plasmids.
Publisher
Cold Spring Harbor Laboratory
Reference70 articles.
1. Insights from 20 years of bacterial genome sequencing
2. Evaluation of strategies for the assembly of diverse bacterial genomes using MinION long-read sequencing
3. Comparison of long-read sequencing technologies in the hybrid assembly of complex bacterial genomes;Microbial Genomics,2019
4. Completing bacterial genome assemblies with multiplex MinION sequencing;Microbial Genomics,2017
5. Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads;PLOS Computational Biology,2017
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献