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
type: Dataset
description: De novo assembly of two individuals from the SweGen dataset
conditions of access: https://publications.europa.eu/resource/authority/access-right/NON_PUBLIC
conditions of access: info:eu-repo/semantics/restrictedAccess
creative work status: completed
  type: DefinedTerm
  in defined term set: http://publications.europa.eu/resource/authority/dataset-status
  term code: COMPLETED
creator: Adam Ameur
creator: Ulf Gyllensten
date modified: 2018-01-01
date published: 2018-01-01
keywords: Medical and Health Sciences
  type: DefinedTerm
  term code: 3
keywords: Nucleotide sequence data
publisher: Uppsala University
version: 0

PropertyValue
property ID: DOI
value: 10.17044/NBIS/G000006

Adam Ameur
type: Person
affiliation: Department of Immunology, Genetics and Pathology, Uppsala University

Ulf Gyllensten
type: Person
affiliation: Department of Immunology, Genetics and Pathology, Uppsala University

Uppsala University
type: Organization