$de\ novo$ assembly and population genomic survey of natural yeast isolates with the Oxford Nanopore MinION sequencer

Archive ouverte

Istace, Benjamin | Friedrich, Anne | d'Agata, Léo | Faye, Sébastien | Payen, Emilie | Beluche, Odette | Caradec, Claudia | Davidas, Sabrina | Cruaud, Corinne | Liti, Gianni | Lemainque, Arnaud | Engelen, Stefan | Wincker, Patrick | Schacherer, Joseph | Aury, Jean-Marc

Edité par CCSD -

International audience. Background: Oxford Nanopore Technologies Ltd (Oxford, UK) have recently commercialized MinION, a small single-molecule nanopore sequencer, that offers the possibility of sequencing long DNA fragments from small genomes in a matter of seconds. The Oxford Nanopore technology is truly disruptive; it has the potential to revolutionize genomic applications due to its portability, low cost, and ease of use compared with existing long reads sequencing technologies. The MinION sequencer enables the rapid sequencing of small eukaryotic genomes, such as the yeast genome. Combined with existing assembler algorithms, near complete genome assemblies can be generated and comprehensive population genomic analyses can be performed. Results: Here, we resequenced the genome of the Saccharomyces cerevisiae S288C strain to evaluate the performance of nanopore-only assemblers. Then we de novo sequenced and assembled the genomes of 21 isolates representative of the S. cerevisiae genetic diversity using the MinION platform. The contiguity of our assemblies was 14 times higher than the Illumina-only assemblies and we obtained one or two long contigs for 65 % of the chromosomes. This high contiguity allowed us to accurately detect large structural variations across the 21 studied genomes. Conclusion: Because of the high completeness of the nanopore assemblies, we were able to produce a complete cartography of transposable elements insertions and inspect structural variants that are generally missed using a short-read sequencing strategy. Our analyses show that the Oxford Nanopore technology is already usable for de novo sequencing and assembly; however, non-random errors in homopolymers require polishing the consensus using an alternate sequencing technology.

Suggestions

Du même auteur

Genome evolution across 1,011 $Saccharomyces\ cerevisiae$ isolates

Archive ouverte | Peter, Jackson | CCSD

International audience. Large-scale population genomic surveys are essential to explore the phenotypic diversity of natural populations. Here we report the whole-genome sequencing and phenotyping of 1,011 $Saccharom...

Viral to metazoan marine plankton nucleotide sequences from the Tara Oceans expedition

Archive ouverte | Alberti, Adriana, A. | CCSD

International audience. A unique collection of oceanic samples was gathered by the Tara Oceans expeditions (2009–2013), targeting plankton organisms ranging from viruses to metazoans, and providing rich environmenta...

European mink (Mustela lutreola) reference genome and population genomics

Archive ouverte | Mouton, Alice | CCSD

International audience. The European mink (Mustela lutreola) is considered as critically endangered in the IUCN red list, and is already extinct in large parts of its ancestral range. A chromosome-scale reference ge...

Chargement des enrichissements...