Probe sequences were taken from the Illumina manifests and mapped onto the Rambouillet genome (GCA_002742125.1) using bwa mem v0.7.17-r1188 with default settings (Indels were ignored) For each SNP a probe pair was constructed by using AlleleA_ProbeSeq and appending either the reference or the alternative allele. Only probe pairs where accepted that passed following filters. -both probes are mapped -one probe is mapped with 0 mismatches -both probes are not multi-mapped -no indels were allowed -both probes had to map in the same orientation -both probes had to map to the same position -mapped probes had between them exactly 1 mismatch, the SNP.
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