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Facilitated sequence assembly using densely labeled optical DNA barcodes: A combinatorial auction approach

Journal article
Authors A. Dvirnas
C. Pichler
C. L. Stewart
S. Quaderi
L. K. Nyberg
V. Muller
S. K. Bikkarolla
Erik Kristiansson
L. Sandegren
F. Westerlund
T. Ambjornsson
Published in Plos One
Volume 13
Issue 3
ISSN 1932-6203
Publication year 2018
Published at Department of Mathematical Sciences
Language en
Links https://doi.org/10.1371/journal.pon...
Keywords resistance plasmids, molecule, alignment, maps, Science & Technology - Other Topics
Subject categories Medical Genetics

Abstract

The output from whole genome sequencing is a set of contigs, i.e. short non-overlapping DNA sequences (sizes 1-100 kilobasepairs). Piecing the contigs together is an especially difficult task for previously unsequenced DNA, and may not be feasible due to factors such as the lack of sufficient coverage or larger repetitive regions which generate gaps in the final sequence. Here we propose a new method for scaffolding such contigs. The proposed method uses densely labeled optical DNA barcodes from competitive binding experiments as scaffolds. On these scaffolds we position theoretical barcodes which are calculated from the contig sequences. This allows us to construct longer DNA sequences from the contig sequences. This proof-of-principle study extends previous studies which use sparsely labeled DNA barcodes for scaffolding purposes. Our method applies a probabilistic approach that allows us to discard "foreign" contigs from mixed samples with contigs from different types of DNA. We satisfy the contig non-overlap constraint by formulating the contig placement challenge as a combinatorial auction problem. Our exact algorithm for solving this problem reduces computational costs compared to previous methods in the combinatorial auction field. We demonstrate the usefulness of the proposed scaffolding method both for synthetic contigs and for contigs obtained using Illumina sequencing for a mixed sample with plasmid and chromosomal DNA.

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