scholarly journals Genetic association between sow longevity and social genetic effects on growth in pigs

2019 ◽  
Vol 32 (8) ◽  
pp. 1077-1083 ◽  
Author(s):  
Joon Ki Hong ◽  
Yong Min Kim ◽  
Kyu Ho Cho ◽  
Eun Seok Cho ◽  
Deuk Hwan Lee ◽  
...  
2000 ◽  
Vol 70 (3) ◽  
pp. 399-406
Author(s):  
K. Meyer ◽  
H. -U. Graser ◽  
A. Na-Chiangmai

AbstractEstimates of genetic parameters were obtained for weight, hip height, heart girth and shoulder to pin length measurements on Thai swamp buffalo, recorded at birth and weaning. Direct heritability estimates were 0·26 for weights at both ages and were low for skeletal measurements, ranging from 0·11 to 0·19. Low values could, in part at least, be caused by inaccuracies in recording. All traits were subject to maternal effects, permanent environmental maternal effects on traits recorded at weaning explaining proportionately up to 0·14 of the total variation. Estimates of genetic (direct and maternal) and permanent environmental correlations between traits recorded at the same time were high throughout, ranging from 0·83 to 0·97 for additive genetic effects and being close to unity otherwise. Except for heart girth measured at weaning, there appeared to be comparatively little genetic association between traits recorded at different times, direct additive correlation estimates ranging from 0·18 to 0·55 in contrast to estimates of 0·38 to 0·65 for correlations with heart girth at weaning.


2015 ◽  
Vol 133 (4) ◽  
pp. 283-290 ◽  
Author(s):  
T.H. Le ◽  
P. Madsen ◽  
N. Lundeheim ◽  
K. Nilsson ◽  
E. Norberg

2019 ◽  
Vol 84 (6) ◽  
pp. 256-271 ◽  
Author(s):  
Camille M. Moore ◽  
Sean A. Jacobson ◽  
Tasha E. Fingerlin

<b><i>Introduction:</i></b> When analyzing data from large-scale genetic association studies, such as targeted or genome-wide resequencing studies, it is common to assume a single genetic model, such as dominant or additive, for all tests of association between a given genetic variant and the phenotype. However, for many variants, the chosen model will result in poor model fit and may lack statistical power due to model misspecification. <b><i>Objective:</i></b> We develop power and sample size calculations for tests of gene and gene × environment interaction, allowing for misspecification of the true mode of genetic susceptibility. <b><i>Methods:</i></b> The power calculations are based on a likelihood ratio test framework and are implemented in an open-source R package (“genpwr”). <b><i>Results:</i></b> We use these methods to develop an analysis plan for a resequencing study in idiopathic pulmonary fibrosis and show that using a 2-degree of freedom test can increase power to detect recessive genetic effects while maintaining power to detect dominant and additive effects. <b><i>Conclusions:</i></b> Understanding the impact of model misspecification can aid in study design and developing analysis plans that maximize power to detect a range of true underlying genetic effects. In particular, these calculations help identify when a multiple degree of freedom test or other robust test of association may be advantageous.


2019 ◽  
Vol 49 (3) ◽  
pp. 327-339 ◽  
Author(s):  
Gunn-Helen Moen ◽  
Gibran Hemani ◽  
Nicole M. Warrington ◽  
David M. Evans

2009 ◽  
Vol 42 (05) ◽  
Author(s):  
M Boxleitner ◽  
I Giegling ◽  
AM Hartmann ◽  
J Genius ◽  
A Ruppert ◽  
...  

Diabetes ◽  
2018 ◽  
Vol 67 (Supplement 1) ◽  
pp. 1706-P ◽  
Author(s):  
ARUSHI VARSHNEY ◽  
STEPHEN PARKER ◽  

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