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March 8, 2026Nature Communications8 citationsOpen Access

High-quality metagenome assembly from nanopore reads with nanoMDBG

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GBGaëtan BenoitRJRobert JamesSRSébastien Raguideau

Key Points

  • The research aims to enhance metagenome assembly using nanopore sequencing through the development of nanoMDBG.
  • Introduced an error correction pre-processing step in minimizer-space for ONT reads.
  • Evaluated performance across various ONT datasets, including a 400 Gbp soil sample.
  • Compared results with other assemblers such as metaFlye.
  • nanoMDBG reconstructed up to twice as many high-quality MAGs compared to metaFlye.
  • Required a third of the CPU time and memory for processing ONT datasets.
  • Performance comparable to PacBio HiFi assemblies at the same sequencing depth.

Abstract

Abstract Third-generation long-read sequencing technologies, significantly improve metagenome assemblies. Highly accurate PacBio HiFi reads can yield hundreds of near-complete metagenome-assembled genomes (MAGs) from a single sample. Recently, the accuracy of the more cost-effective Oxford Nanopore Technologies (ONT) platform has increased to a per-base error rate of 1-2%. However, current metagenome assemblers are optimized for HiFi and do not scale to the large data sets that ONT enables. We present nanoMDBG, an evolution of metaMDBG, which supports the latest ONT reads through an error correction pre-processing step in minimizer-space. Across a range of ONT datasets, including a large 400 Gbp soil sample, nanoMDBG reconstructs up to twice as many high-quality MAGs as the next best ONT assembler, metaFlye, while requiring a third of the CPU time and memory. Critically, the latest ONT technology can now produce comparable MAG construction results as those obtained using PacBio HiFi at the same sequencing depth.

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Cite This Study

Benoit et al. (2026) studied this question.

synapsesocial.com/papers/69acc58f32b0ef16a404fe95https://doi.org/10.1038/s41467-026-69760-y
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