Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2023.07.09.548288v1?rss=1
Authors: Do, V. H., Nguyen, S. H., Le, D. Q., Nguyen, T. T., Nguyen, C. H., Ho, T. H., Nam, V. S., Nguyen, T., Nguyen, H. A., Cao, M. D.
Abstract:
Whole genome sequencing has increasingly become the essential method for studying the genetic mechanisms of antimicrobial resistance and for surveillance of drug-resistant bacterial pathogens. The majority of bacterial genomes sequenced to date have been sequenced with Illumina sequencing technology, owing to its high-throughput, excellent sequence accuracy, and low cost. However, because of the short-read nature of the technology, these assemblies are fragmented into large numbers of contigs, hindering the obtaining of full information of the genome. We develop Pasa, a graph-based algorithm that utilizes the pangenome graph and the assembly graph information to improve scaffolding quality. By leveraging the population information of the bacteria species, Pasa is able to utilize the linkage information of the gene families of the species to resolve the contig graph of the assembly. We show that our method outperforms the current state of the art in terms of accuracy, and at the same time, is computationally efficient to be applied to a large number of existing draft assemblies.
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