SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
The SweGen contains whole-genome variant frequencies for 1000 Swedish individuals generated within the SweGen project. The data is intended to be used as a resource for the research community and clinical genetics laboratories.
DNA from blood samples were whole genome sequenced using Illumina X technology at SciLifeLab Uppsala and SciLifeLab Stockholm. The sequencing data was analyzed with the GATK best practices pipeline to obtain a joint called variant frequency dataset. For more information, see: https://www.nature.com/articles/ejhg2017130Opens in a new tab
Go to data source
Opens in a new tabhttps://swefreq.nbis.se
Citation and access
Citation and access
Method and outcome
Method and outcome
Data collection - Registry extract and/or access to biobank sample
Data collection - Registry extract and/or access to biobank sample
Administrative information
Administrative information
Topic and keywords
Topic and keywords
Relations
Relations
Publications
Publications
Metadata
Metadata
Version 1
Uppsala University