PropertyValue
nif:beginIndex
  • 0 (xsd:integer)
nif:broaderContext
nif:endIndex
  • 185 (xsd:integer)
nif:isString
  • We randomly sub-sampled 1,000, 2,500, 5,000, 10,000, and 50,000 SNPs and also randomly picked one allele per site in order to mimic extremely low coverage sequencing of ancient samples.
rdf:type