Assemblies of long-read metagenomes suffer from diverse errors
Genomes from metagenomes have revolutionised our understanding of microbial diversity, ecology, and evolution, propelling advances in basic science, biomedicine, and biotechnology. Assembly algorithms that take advantage of increasingly available long-read sequencing technologies bring the recovery...
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Main Authors | , , , |
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Language | English |
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Cold Spring Harbor Laboratory
24.04.2025
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Abstract | Genomes from metagenomes have revolutionised our understanding of microbial diversity, ecology, and evolution, propelling advances in basic science, biomedicine, and biotechnology. Assembly algorithms that take advantage of increasingly available long-read sequencing technologies bring the recovery of complete genomes directly from metagenomes within reach. However, assessing the accuracy of the assembled long reads, especially from complex environments that often include poorly studied organisms, poses remarkable challenges. Here we show that erroneous reporting is pervasive among long-read assemblers and can take many forms, including multi-domain chimeras, prematurely circularized sequences, haplotyping errors, excessive repeats, and phantom sequences. Our study highlights the need for rigorous evaluation of the algorithms while they are in development, and options for users who may opt for more accurate reads than shorter runtimes. |
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AbstractList | Genomes from metagenomes have revolutionised our understanding of microbial diversity, ecology, and evolution, propelling advances in basic science, biomedicine, and biotechnology. Assembly algorithms that take advantage of increasingly available long-read sequencing technologies bring the recovery of complete genomes directly from metagenomes within reach. However, assessing the accuracy of the assembled long reads, especially from complex environments that often include poorly studied organisms, poses remarkable challenges. Here we show that erroneous reporting is pervasive among long-read assemblers and can take many forms, including multi-domain chimeras, prematurely circularized sequences, haplotyping errors, excessive repeats, and phantom sequences. Our study highlights the need for rigorous evaluation of the algorithms while they are in development, and options for users who may opt for more accurate reads than shorter runtimes. |
Author | Sachdeva, Rohan Banfield, Jillian F. Trigodet, Florian Eren, A. Murat |
Author_xml | – sequence: 1 givenname: Florian orcidid: 0000-0002-4933-2896 surname: Trigodet fullname: Trigodet, Florian organization: Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research – sequence: 2 givenname: Rohan surname: Sachdeva fullname: Sachdeva, Rohan organization: Innovative Genomics Institute, University of California Berkeley – sequence: 3 givenname: Jillian F. surname: Banfield fullname: Banfield, Jillian F. email: meren@hifmb.de organization: Biomedicine Discovery Institute, Monash University – sequence: 4 givenname: A. Murat orcidid: 0000-0001-9013-4827 surname: Eren fullname: Eren, A. Murat email: meren@hifmb.de organization: Max Planck Institute for Marine Microbiology |
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Cites_doi | 10.1101/gr.258640.119 10.1128/mBio.00725-19 10.1101/2025.01.15.633187 |
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Notes | Competing Interest Statement: The authors have declared no competing interest. |
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Title | Assemblies of long-read metagenomes suffer from diverse errors |
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