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The allele-specific gene-tagged markers were well developed for GS3, GW2, and qSW5/GW5 genes as mentioned above.
The markers were well distributed over all the 21 linkage groups.
The transferable markers were well distributed in LGs 3 and 16.
These 3228 markers were well distributed on the B. napus linkage map with an average of one SNP every 0.62 centimorgan (cM).
The markers were well distributed over all the 12 linkage groups with only two intervals ≥ 25 cM in chromosomes 5 and 10.
Since the RFLP markers were well distributed across the linkage groups, they can be used as potential anchor markers for integration or comparison of maps of different populations.
Similar(49)
Our analysis showed that most maize lines in a diverse sample are separated by a large genetic distance and, consistent with the results of Jones et al. [19], that measures of distance based on different markers were well-correlated only for the small subset of individuals that were closely related.
The markers were well-dispersed throughout the genome, and the average distance between markers was 7.12 cM.
In general, the DArT markers were well-distributed across the genome, however, certain chromosomal regions showed extensive clustering such as on chromosomes A9 and C2 (Additional file 4).
This tissue was chosen because the large polytene chromosomes allow exceptional spatial resolution, and the wild type distribution of certain euchromatic and heterochromatic markers is well characterized.
Statistical analyses (Fisher test pairwise comparisons of repeat score distributions between haplogroups) indicate that both penta/hexa and tri/tetra STR markers are well capable of distinguishing haplogroups without SNP marker data; in practice, however, the network based on penta/hexa markers reflects the haplogroup affiliations of haplotypes better.
More suggestions(14)
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