Overview

Title 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
Authors , and
Description De novo assembly of two individuals from the SweGen dataset
Year 2018
doi 10.17044/NBIS/G000006
Access constraints Restricted access
Cite as Adam Ameur, and Ulf Gyllensten (2018) 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 doi:10.17044/NBIS/G000006
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