Although all these "GS" mouse models, including ours, have several characteristics in common with human GS, it has yet to be established whether they suffice as model systems for the defect.
Where there is no entry for the binary level graph set (GS) it is assumed that this synthon will be found at higher levels.
If the dataset is suited for GS, it is likely that the individuals are already related.
However, due to the largely underdetermined systems with more correlated markers than phenotyped individuals that underpin GS, it is essential to increase the number of genotyped and phenotyped individuals, even at the expense of a lower quality of genomic information.
Note that s[(i − 1)(B + 3) + 1, i(B + 3) − 1] is a substring of s that consists of (B + 2) base Gs; it is located either strictly between two consecutive base Ts or strictly between one base T and one end of the string s.
Since one of the objectives of the panel design was to increase its utility for genome-wide-association studies (GWAS) or GS, it was essential to target equi-distant SNPs across the whole genome.
