Optimizing experimental design for genome sequencing and assembly with Oxford Nanopore Technologies

Abstract

BackgroundHigh quality reference genome sequences are the core of modern genomics. Oxford Nanopore Technologies (ONT) produces inexpensive DNA sequences in excess of 100,000 nucleotides but high error rates make sequence assembly and analysis a non-trivial problem as genome size and complexity increases. To date there has been no comprehensive attempt to generate robust experimental design for ONT genome sequencing and assembly. In this study, we simulate ONT and Illumina DNA sequence reads for the model organisms Escherichia coli, Caenorhabditis elegans, Arabidopsis thaliana, and Drosophila melanogaster and assemble with Canu, Flye, and MaSuRCA software to quantify the influence of sequencing coverage and assembly approach. Heterozygosity in outbred eukaryotes is a common problem for genome assembly. We show broad applicability of our methods using real ONT data generated for four strains of the highly heterozygous nematode Caenorhabditis remanei and C. latens. ResultsO_LIONT libraries have a unique error structure and high sequence depth is necessary to assemble contiguous genome sequences. C_LIO_LIAs sequence depth increases errors accumulate and assembly statistics plateau. C_LIO_LIHigh-quality assembled sequences require a combination of experimental techniques that increase sequence read length and computational protocols that reduce error through correction, read selection and polishing with higher accuracy short sequence reads. C_LIO_LIOur robust experimental design results in highly contiguous and accurate genome assemblies for the four strains of C. remanei and C. latens. C_LI ConclusionsONT sequencing is inexpensive and accessible but the technologys error structure requires robust experimental design. Our quantitative results will be helpful for a broad array of researchers seeking guidance for de novo assembly projects.