A complete bacterial genome assembled de novo using only nanopore sequencing data
Research output: Contribution to journal › Article
Colleges, School and Institutes
We have assembled de novo the Escherichia coli K-12 MG1655 chromosome in a single 4.6-Mb contig using only nanopore data. Our method has three stages: (i) overlaps are detected between reads and then corrected by a multiple-alignment process; (ii) corrected reads are assembled using the Celera Assembler; and (iii) the assembly is polished using a probabilistic model of the signal-level data. The assembly reconstructs gene order and has 99.5% nucleotide identity.
|Number of pages||3|
|Publication status||Published - Aug 2015|