P0472
Localized Assemblies of the 20 Gbp Sitka Spruce (Picea sitchensis) Genome Using Chromium Reads

Shaun D Jackman , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Benjamin P Vandervalk , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
René L Warren , Genome Sciences Centre, BC Cancer Agency, Vancouver, BC, Canada
Hamid Mohamadi , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Justin Chu , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Sarah Yeo , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Lauren Coombe , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Stephen Pleasance , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Robin J Coope , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Joerg C Bohlmann , University of British Columbia, Vancouver, BC, Canada
Steven JM Jones , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Inanc Birol , BC Cancer Agency Genome Sciences Centre, Vancouver, BC, Canada
Long-read sequencing technologies have greatly improved assembly contiguity, but at a cost roughly ten times that of short-read sequencing technology. For population studies and when sequencing large genomes, such as conifer genomes and other economically important crop species, this cost may be prohibitive. The 10x Genomics Chromium technology generates linked reads from large molecules at a cost comparable to standard short-read sequencing technologies. Whereas paired-end sequencing gives two reads from a small DNA fragment, Chromium yields roughly a hundred reads from molecules with a typical size of 10 to 100 kilobases. This technology has been applied to assemble genomes as large as the human genome.

Here we demonstrate its utility to localize assemblies of large genomic loci, including the organellar genomes of the 20 gigabase Sitka spruce (Picea sitchensis) genome. We have reported earlier the assembly of the plastid genome of Sitka spruce using the Gemcode technology, the precursor of Chromium. Using the Chromium technology, we have now assembled localized nuclear segments of the Sitka spruce and its mitochondrial genome.

Animal mitochondrial genomes are typically quite small, tens of kilobases, and plant mitochondria are often much larger, hundreds of kilobases. Conifer mitochondria are, in contrast, surprisingly large, nearly six megabases for white spruce (Picea glauca). With a mere two gymnosperm mitochondria in NCBI Genbank and a single conifer mitochondrion, few examples of these mysteriously large organellar genomes are available. Our results will thus be of interest to evolutionary biology researchers beyond the field of forestry genomics.

Chromium reads permit cost-effective assembly of large genomes with high-throughput, short-read sequencing technology, while also providing large-molecule scaffolding data. Here we assemble Chromium reads using ABySS 2.0, which uses one-tenth the memory of previous versions, and only a few hundred gigabytes of RAM for large conifer genomes.

Handouts
  • PAG 2017 Poster.pdf (9.6 MB)