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The average percent of difference to GS for all overestimated values for each group was calculated and expressed as the mean ± SD.
In particular, GS increased the standardized accuracy of prediction from 0.12 with MAS to 0.59 for grain yield in population A and from 0.28 with MAS to 0.70 for total pentosan content in population B. Comparable, albeit less drastic, increases of accuracy were obtained with GS for all other traits in both populations.
At RT, the as-grown devices studied in this work lase from QD GS for all cavity lengths whereas the annealed devices show simultaneous lasing from different energy levels (for L ≤ 1.5 mm for un-implanted and L ≤ 2 mm for implanted devices).
Module significance (MS) was calculated as the mean GS for all module genes.
GS i is the absolute value of correlation between a gene and a phenotype, and MS is average absolute GS i GS for all genes in a particular module.
Similar(55)
A Hodge-like operator υ on M is (G, h -invariance-preserving if g* ∘ υ = υ ∘ g* and h -invariance-preservingll g ∈ G.
From (24) and hypothesis (23), we have g x n ≺ g x for all n, g x ≼ g ( g x ).
Thus, d s ( J g, J h ) ≤ α d s ( g, h ) for all g and h in G.
We say that b∈G is an upper bound for G′ whenever g′∈ [ b] G for all g′∈G′.
Taking ( X i, G i ) = ( X, G ) for all i, we derive the following result.
This contradiction leads to G ( 1 ) ≤ G for all τ ∈ [ − 1, 1 ].
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