DNA variants discovered by project, type, population and novelty

Range Table - link
Organism Human Homo sapiens
Reference 1000 Genomes Project Consortium, Durbin RM, Abecasis GR, Altshuler DL, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA. A map of human genome variation from population-scale sequencing. Nature. 2010 Oct 28 467(7319):1061-73. doi: 10.3109/03014460.2013.807878. p.1063 table 1PubMed ID20981092
Method P.1061 right column bottom paragraph: "A total of 4.9 terabases of DNA sequence was generated in nine sequencing centres using three sequencing technologies, from DNA obtained from immortalized lymphoblastoid cell lines (Table 1 and Supplementary Table 1)."
Comments P.1062 right column 5th paragraph: "Much of the data for the trio project were collected before technical improvements in [investigators'] ability to map sequence reads robustly to some of the repeated regions of the genome (primarily longer, paired reads). For these reasons, stringent alignment was more difficult and a smaller portion of the genome was accessible in the trio project: 80% of the reference, 85%of coding sequence and 97% of HapMapII sites (Table 1)." P.1065 left column bottom paragraph: "Genotypes, and, where possible, haplotypes, were inferred for most variants in each project (see Supplementary Information and Table 1)."
Entered by Uri M
ID 110122