The results of a χ test showed that segregation distortion markers were distributed on every LG with a distribution very similar to that of all markers (Table 4) except for LG6 and LG11.
These markers were distributed evenly on rice 12 chromosomes and polymorphism between Nipponbare and Kasalath was displayed.
Asplenium DArT markers were distributed as follows: A. trichomanes private (65%), A. viride private (16%), A. trichomanes/A.
An haplotype analysis however revealed that the 4 markers were distributed in two blocks (table 3) of LD.
A map position could be assigned for 69 markers from this dataset; these markers were distributed over different positions in the linkage groups of a doubled haploid population (Pino Del Carpio, unpublished results).
The SZGenes are overall longer than other human genes, thus, they might have more chance to have small P values, assuming GWAS markers were distributed approximately evenly in the human genome.
The distorted markers were distributed throughout the maps.
These markers were distributed on 5 linkage groups.
The segregation distortion markers were distributed among every LG.
Importantly, clusters of unique SNP markers were distributed very specifically for each of the studied genotypes.
The newly developed EST-based markers were distributed across all nine LGs.
