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  4. De novo haplotype reconstruction in viral quasispecies using paired-end read guided path finding
 
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De novo haplotype reconstruction in viral quasispecies using paired-end read guided path finding

Author(s)
Zhao, Yingchao  
Author(s)
Chen, J.
Sun, Y.
Date Issued
2018
Publisher
Oxford University Press
Journal
Bioinformatics
Volume
34
Issue
17
Start page
2927
End page
2935
Abstract
Motivation RNA virus populations contain different but genetically related strains, all infecting an individual host. Reconstruction of the viral haplotypes is a fundamental step to characterize the virus population, predict their viral phenotypes and finally provide important information for clinical treatment and prevention. Advances of the next-generation sequencing technologies open up new opportunities to assemble full-length haplotypes. However, error-prone short reads, high similarities between related strains, an unknown number of haplotypes pose computational challenges for reference-free haplotype reconstruction. There is still much room to improve the performance of existing haplotype assembly tools. Results In this work, we developed a de novo haplotype reconstruction tool named PEHaplo, which employs paired-end reads to distinguish highly similar strains for viral quasispecies data. It was applied on both simulated and real quasispecies data, and the results were benchmarked against several recently published de novo haplotype reconstruction tools. The comparison shows that PEHaplo outperforms the benchmarked tools in a comprehensive set of metrics. Availability and implementation The source code and the documentation of PEHaplo are available at https://github.com/chjiao/PEHaplo. Supplementary information Supplementary data are available at Bioinformatics online.
URI
https://repository.sfu.edu.hk/handle/sfu/238
DOI
10.1093/bioinformatics/bty202
SFU Affiliated Publication
Yes
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