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These markers were spread all over the genome, except for chromosomes 3D, 4B, 4D, and 5D.
In both maps, the distorted markers were spread over the genome.
Seven gaps with a distance >5 cM between adjacent markers were spread across C02, and seven gaps with distances >10 cM between adjacent markers occurred on six of the linkage groups: C01, C02, C07, C08 and C09 each with one gap, and C06 with two gaps (Table 7).
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For example, on chromosome VIII, 18 markers are spread on the top 71 cM while 167 markers are spread on the next 29 cM.
These markers are spread across regions that frequently show LOH in glial tumours.
The 1296 markers are spread in 1255 positions of which 1220 positions consist of a single marker, 32 positions contain two co-localized markers and three positions contain 3 to 6 co-localized markers.
The SNP markers we used were spread across the R. communis genome in 47 unique contigs ranging in size from 2.5 kb to 133 kb.
9 markers, 1.0 mm in diameter, were spread out into the tibial metaphysis in all knees.
If 300 K markers were used and 10 000 x were spread across 500 individuals (20.0 x per individual), response to selection was equal to 1.11 when training was on SNP array data with 1000 individuals, and equal to 0.73 when training was on GBS data with the same number of individuals and x as in the prediction set.
Blankets were spread.
Resources were spread evenly.
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