|Title||Whole genome sequencing of (IBS) Iberian populations in Spain HapMap population|
The purpose of the project is to support the discovery and understanding of genetic variants that influence human disease. Specifically defined goals are (a) the discovery of single nucleotide variants at frequencies of 1% or higher in diverse populations, (b) even more comprehensive discovery (variants down to frequencies of 0.1 - 0.5%) in functional gene regions, and (c) discovery of structural variants, such as copy number variants, other insertions and deletions, and inversions, including sequence-level understanding of breakpoints.
|Organisms||Homo sapiens, unidentified|
|Type||Whole Genome Sequencing|
|Submitter||1000 Genomes Project|