SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population

Description

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/ejhg2017130

Resources

Name Format Description Link

Tags

  • genetics,-population
  • befolkningsgenetik

Topics

  • HEAL

Categories