NaS is a hybrid approach developped to take advantage of data generated using MinION device. We combine Illumina and Oxford Nanopore technologies to produce NaS (Nanopore Synthetic-long) reads of up to 60 kb that align with no error to the reference genome and spanned repetitive regions.
NaS v2 is out, this latest release has several improvments (like sensitivity in read recruitement and post-assembly steps). Use the download link to get the software bundle, which includes installation and usage instructions.
Follow this link to download the software from our GitHub.
We also provide a DockerHub for NaS.All datasets and assemblies presented in the article can be downloaded.
Contact : nas [at] genoscope [.] cns [.] fr