SWALO: scaffolding with assembly likelihood optimization
- Creators
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Rahman, Atif
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Pachter, Lior
Abstract
Scaffolding, i.e. ordering and orienting contigs is an important step in genome assembly. We present a method for scaffolding using second generation sequencing reads based on likelihoods of genome assemblies. A generative model for sequencing is used to obtain maximum likelihood estimates of gaps between contigs and to estimate whether linking contigs into scaffolds would lead to an increase in the likelihood of the assembly. We then link contigs if they can be unambiguously joined or if the corresponding increase in likelihood is substantially greater than that of other possible joins of those contigs. The method is implemented in a tool called SWALO with approximations to make it efficient and applicable to large datasets. Analysis on real and simulated datasets reveals that it consistently makes more or similar number of correct joins as other scaffolders while linking very few contigs incorrectly, thus outperforming other scaffolders and demonstrating that substantial improvement in genome assembly may be achieved through the use of statistical models. SWALO is freely available for download at https://atifrahman.github.io/SWALO/.
Additional Information
© The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. Received: 22 December 2020; Revision received: 16 June 2021; Accepted: 16 August 2021; Published: 20 August 2021. We thank Dan Rokhsar, Páll Melsted, Harold Pimentel, Shannon McCurdy and Nicolas Bray for helpful conversations during the development of SWALO. Funding: NIH [R01 HG006129 to L.P., in part]; Fulbright Science & Technology Fellowship [15093630 to A.R., in part]. Funding for open access charge: NIH [R01 HG006129]. Conflict of interest statement: None declared.Attached Files
Published - gkab717.pdf
Submitted - 081786v2.full.pdf
Supplemental Material - gkab717_supplemental_file.pdf
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Additional details
- Eprint ID
- 111143
- Resolver ID
- CaltechAUTHORS:20210930-221100053
- NIH
- R01 HG006129
- Fulbright Foundation
- 15093630
- Created
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2021-10-04Created from EPrint's datestamp field
- Updated
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2021-11-18Created from EPrint's last_modified field
- Caltech groups
- Division of Biology and Biological Engineering (BBE)