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All 155 gene-containing scaffolds based on the reported physical mapping were included and were in complete agreement with our orthology-based chromosomal assignments.
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Application to a common element of the set of fixed points of a Lipschitzian pseudocontractive mapping and solutions of variational inequality for γ-inverse strongly monotone mapping is included.
HR, BL and MAP were included in the model, whereas CVP was excluded.
Also the reevaluated markers which had been excluded were added again, and the markers which did not affect the framework map were included in the final map.
The minimum LOD of 4 was used, and only the markers which did not affect the orders in the framework map were included.
Reference maps were included because they provided numerous pivotal markers, which improved connections between maps.
Maternal a priori risk factors, including MAP, were included in the assessment.
A total of 3863 and 11,344 SNPs that mapped were included in the intraspecific and interspecific maps, respectively.
†† Only QTL maps that had a minimum of two common markers with at least a chromosome of another map were included into the meta-analysis.
As described previously [ 29, 30], genes with a mean abundance > 0.1 FPKM (Fragments per kilobase of transcript per million fragments mapped) were included in the analysis.
Next, the subjects' Z-maps were included in a random effects, one-sample t-test to identify voxels whose means differed from zero with P < 0.0005.
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