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Genetic architecture of disease in Greenland is shaped by demographic history, fine-structure, and selection - WGS data

This file set has 448 Greenlandic individuals sequenced using Illumina 150 Paired end sequencing and has an average sequencing depth of 35X. The data is unfiltered, in VCF format, and covers 19.751.308 variants.

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Slightly modified standard Data Access Agreement (DDA). Full form as a .doc document, shared via Dropbox.

Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS50000000657 Population Genomics

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF50000219435 vcf.gz 63.7 GB
1 File (63.7 GB)