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The risk estimate was corrected for sex, age, smoking habits, and workplace exposure.
The hormesis frequency estimate was corrected for false-positive and false-negative values.
Although likely a biased estimate of the actual density of small mammals at our trapping sites, this estimate was corrected for trapping effort in order to be comparable across sites.
The size estimate was corrected by the chromosome coverage by the mapped contigs (total length of the mapped contigs/entire length of the chromosome arm), where the mapped contigs covered 54 % of the entire chromosome arm.
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The noise estimate is corrected with the noise coherence function [21]: Ŝ n ̂ n ̂ ′ = Ŝ n ̂ n ̂ 2 ( 1 + ℜ { Γ diffuse } ), (34).
The error in the estimate increases when the RF estimate is corrected for correlations only (θ = ∞ and φ = 1, denoted by the circle).
The error in the estimate increases when the RF estimate is corrected for correlations only (θ = ∞ and φ = 1, denoted by the circle) and the RF estimate ĝc (shown in blue) is biased.
Because the upper bound for positive efficacy estimates is 1 but the lower bound for negative efficacies is −∞, each of the negative efficacy estimates was corrected.
π and D xy estimates were corrected for multiple hits using a Jukes Cantor correction (Jukes and Cantor 1969).
All dN an dS estimates were corrected for multiple substitutions using the Jukes-Cantor correction implemented in bioperl [ 36].
Average pairwise diversity and divergence (D xy ) estimates were corrected for multiple hits using a Jukes-Cantor correction [ 67].
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