PropertyValue
nif:beginIndex
  • 0 (xsd:integer)
nif:broaderContext
nif:endIndex
  • 211 (xsd:integer)
nif:isString
  • In such situations, a common approach in many ancient DNA studies is to randomly sample one sequencing read per individual and SNP site and then use the allele carried on that read as pseudo-haploid information.
rdf:type