Changes

== Scaffold for Identity by Descent ==

== Scaffold for Identity by Descent ==

We selected a grid of 5,805 markers (distributed approximately one per 500 kb across the autosomes and the X chromosome) that showed little differentiation between African-, European- and Asian-ancestry sequenced by the 1000 Genomes Project and allele frequency close to 0.50. Markers previously genotyped on the Illumina Omni 2.5M array were favored and markers with A/T or G/C alleles were avoided.

We selected a grid of 5,710 markers (distributed approximately one per 500 kb across the autosomes and the X chromosome) that showed little differentiation between African-, European- and Asian-ancestry sequenced by the 1000 Genomes Project and allele frequency close to 0.50. Markers previously genotyped on the Illumina Omni 2.5M array were favored and markers with A/T or G/C alleles were avoided.

These markers can be used to identify stretches of identity by descent between apparently unrelated individuals or to support linkage-based analyses in appropriate family samples.

These markers can be used to identify stretches of identity by descent between apparently unrelated individuals or to support linkage-based analyses in appropriate family samples.

== Functionally interesting variants ==

== Functionally interesting variants ==