A key benefit of the Eucalyptus DArT markers is the public availability of the sequences of most of the 7680 markers contained on the genotyping array [GenBank accession numbers HR865291 - HR872186], thus making it possible to anchor DArT markers directly to the reference E. grandis genome sequence [v1.0 released January 2011; [ 36].
Most of the mapped markers contained in the reference map are polymorphic in diverse collection of germplasm, and thus are potentially transferrable to a broad array of genetic experimentation (e.g., integration of physical and genetic maps, colinearity analysis, map-based gene cloning, epistasis dissection, and marker-assisted selection).
In contrast, in our study, most injected myogenic cells expressing neuronal markers contained only one normal looking nucleus.
Here, most of the markers contain dinucleotides and trinucleotides and only seven loci contain tetranucleotide repeats such as (AATT n, (TTCC n, (GATG n, (ATGT n, (GTAT n, (ATTT n, (TTTG n[ 6, 29, 30, 47- 49].
These markers contained 4483 alleles (Table 2).
Markers containing dinucleotide repeats exhibited significantly higher levels of genetic variation in A, He, and Ho than most other motif lengths (Table 2, Figs. 2 and 3).
All LGs are shown in Table 2: LG10 contained the most markers for the female map (242 markers), LG11 for the male map (80 markers) and LG10 for the integrated map (243 markers).
Although this linkage map contained more markers than ours, most markers on their map were SRAP markers, which could not be transferred to other linkage map easily.
HG 2 also had the most markers mapped with 475 markers compared to HG7 which contained the least number of markers at 204 (Table 3).
Most markers had a low MAF.
