COPE: An accurate k-mer-based pair-end reads connection tool to facilitate genome assembly

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Abstract

Motivation: The boost of next-generation sequencing technologies provides us with an unprecedented opportunity for elucidating genetic mysteries, yet the short-read length hinders us from better assembling the genome from scratch. New protocols now exist that can generate overlapping pair-end reads. By joining the 3′ ends of each read pair, one is able to construct longer reads for assembling. However, effectively joining two overlapped pair-end reads remains a challenging task.Result: In this article, we present an efficient tool called Connecting Overlapped Pair-End (COPE) reads, to connect overlapping pair-end reads using k-mer frequencies. We evaluated our tool on 30× simulated pair-end reads from Arabidopsis thaliana with 1% base error. COPE connected over 99% of reads with 98.8% accuracy, which is, respectively, 10 and 2% higher than the recently published tool FLASH. When COPE is applied to real reads for genome assembly, the resulting contigs are found to have fewer errors and give a 14-fold improvement in the N50 measurement when compared with the contigs produced using unconnected reads. © 2012 The Author.

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APA

Liu, B., Yuan, J., Yiu, S. M., Li, Z., Xie, Y., Chen, Y., … Luo, R. (2012). COPE: An accurate k-mer-based pair-end reads connection tool to facilitate genome assembly. Bioinformatics, 28(22), 2870–2874. https://doi.org/10.1093/bioinformatics/bts563

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