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The presence of genetic correlations between traits resulted in 13.2% of SNPs selected for AFI and 4.5% of SNPs selected for RFI also being selected for ADG in the analysis of breeding values.
Bayesian clustering analysis of breeding individuals without regard to subspecies or region of origin revealed a maximum log Pr(X|K) for K = 2 reflecting two distinct population clusters.
Further, Bayesian modeling also solves many of the issues regarding analysis of breeding values discussed in Postma (2006), Wilson et al. (2009), and Hadfield et al. (2010) as both breeding values and functions of breeding values (e.g., mean breeding values over hatch years) are considered random variables, and hence both uncertainty and dependencies are accounted for.
This could be the case in Reed et al. (2006) study using the North-Atlantic-Oscillation Index, which summarizes climate variations across Western Europe and Eastern North America, in their analysis of breeding time in the common guillemot, Uria aalge showing no individual variation in reaction norm slopes.
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Because a very small amount of tissue is required for barcode analysis, purity of breeding lines can be determined at an early stage of seedling growth.
This paper describes the efficacy of the C6AIR for QTL mapping, genetic diversity analysis, SNP fingerprinting of breeding lines, tracking of introgressions, and checking for recovery of recurrent parent background during marker-assisted backcrossing.
Effective population size is a compound population genetic parameter generally considered linearly proportional to census population size – in this analysis, the population of breeding females.
The structural analysis of the breeding blanket is complex in terms of its geometry and loading conditions.
We, therefore, question the use of Pan I and other loci under such intense selection as markers for analysis of population breeding structure due to reduced gene flow [18], [19], particularly if depth, the confounding of depth and geographic location, and habitat-specific fishing pressures are not controlled for.
Analysis of the breeding system and fruit development of the species is a requisite in these attempts and important for the future genetic improvement programme of the species.
Levels of hybridisation at Marion and Amsterdam islands are low (~2% [ 16, 17], but recent genetic analysis of the breeding population at Macquarie Island revealed up to 21% of pups born to be gazella/tropicalis hybrids [ 18].
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