The 1000 Genomes Project is an international collaboration which has established the most detailed catalogue of human genetic variation, including SNPs, structural variants, and their haplotype contex
Table S1. List of the high coverage samples analysed in this study along with their geographic origin and Y-chromosome haplogroup affiliation. (XLSX 20 kb)
A small genotype data repository containing data used in recent papers from the Estonian Biocentre. Most of the data pertains to human population genetics. PDF files of the papers are also freely avai
Each record contains: (a) an observed sequence of STR locus SE33, (b) annotation of the repeat region (“bracketing”) and flanking region polymorphisms, (c) information regarding the sequencing assay a
