Estonian Biocentre Public

For academic research, please find here human DNA sequence and genotype data from recent papers.
Complete high coverage human genomes and Y chromosome sequence data has been generated by Complete Genomics
SNP data has been generated with different Illumina genotyping arrays since 2008. Data has been lifted to Build37 and rsNumbers come from hg19 b131 (see the log below). The data is in PLINK binary PED (bed, bim, fam) format.
Please cite the papers and contact mait@ebc.ee for any questions.

IMPORTANT NOTE

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307 high coverage human Y chrmosome sequences. *******************************	paper: \|\| Data
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Complete 40X human genomes data in COMPLETE GENOMICS format *******************************	paper: \|\| Data
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Have a look at the loose log of how we arrive at the data: READ ME