File(s) not publicly available
Data from: De novo assembly of two Swedish genomes reveals missing segments from the human GRCh38 reference and improves variant calling of population-scale sequencing data
datasetposted on 21.09.2018 by Adam Ameur, Ulf Gyllensten
Datasets usually provide raw data for analysis. This raw data often comes in spreadsheet form, but can be any collection of data, on which analysis can be performed.
De novo assembly of two individuals from the SweGen dataset