Additional file 1 of X chromosome inactivation across primary human tissues is mostly complete, with significant implications for genetic and clinical studies
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
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
This research investigates the influence of demographic factors on human genetic sub-structure. In our discovery cohort, we show significant demographic trends for decreasing autozygosity associated w
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