scholarly journals Identification and characterisation of novel SNP markers in Atlantic cod: Evidence for directional selection

BMC Genetics ◽  
2008 ◽  
Vol 9 (1) ◽  
Author(s):  
Thomas Moen ◽  
Ben Hayes ◽  
Frank Nilsen ◽  
Madjid Delghandi ◽  
Kjersti T Fjalestad ◽  
...  
BMC Genetics ◽  
2017 ◽  
Vol 18 (1) ◽  
Author(s):  
Diana Duarte-Delgado ◽  
Deissy Juyó ◽  
Christiane Gebhardt ◽  
Felipe Sarmiento ◽  
Teresa Mosquera-Vásquez

2009 ◽  
Vol 9 (1) ◽  
pp. 276 ◽  
Author(s):  
Einar E Nielsen ◽  
Jakob Hemmer-Hansen ◽  
Nina A Poulsen ◽  
Volker Loeschcke ◽  
Thomas Moen ◽  
...  

2012 ◽  
Vol 159 (6) ◽  
pp. 1347-1362 ◽  
Author(s):  
Małgorzata Zbawicka ◽  
Agata Drywa ◽  
Beata Śmietanka ◽  
Roman Wenne

2020 ◽  
Vol 18 (10) ◽  
pp. 770-778
Author(s):  
Wen-Ru WU ◽  
Chun-Song CHENG ◽  
Qi-Qing CHENG ◽  
Chi-Chou LAO ◽  
Hao CUI ◽  
...  

2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 33-33
Author(s):  
Miguel Toro Ibáñez

Abstract We deal with several problems that arise when inferring genetic parameters at the level of quantitative trait loci (QTL) from molecular data such as SNP markers. Linkage Disequilibrium (LD) is recognized as a factor creating ambiguity in the partition of genetic variance. Here, using a simple model with three loci (one QTL and two markers), it is shown that the markers generate apparent AxA and DxD epistasis, even if only third order disequilibrium exists and the QTL is dominant. The problem of “phantom epistasis” is not alleviated by larger sample sizes (de los Campos et al., 2019). We also show that markers can give a distorted picture of the genetic correlation between traits: The genomic correlation could be greater, lower or even of opposite sign than the true genetic correlation. Therefore, speculating about genetic correlations and even about their causes (e.g., pleiotropy) using genomic data is often conjectural. Thirdly, we examine the problem of directional selection generating negative linkage disequilibrium (“Bulmer effect”) in the short term from a genomic selection perspective. It seems that the reduction in response due to the Bulmer effect is the same for genomic selection as for selection based on traditional BLUP. However, the reduction in response with genomic selection is greater than when selection is based directly on phenotypes only (Van Grevenhof et al. 2012). It is also expected that directional selection for a polygenic trait should increase recombination rate, provided there is genetic variance for recombination. It is then of relevance to ask whether recombination rates could be manipulated in order to increase selection response (Battagin et al., 2016). Finally, we consider that recombination and epistasis are closely intertwined: Epistasis generate LD and recombination break them up. Then, we should expect genomes to be modular: regions with low recombination containing functionally related genes loosely linked to other regions.


2014 ◽  
Vol 24 (3) ◽  
pp. 535-544 ◽  
Author(s):  
R. Scozzari ◽  
A. Massaia ◽  
B. Trombetta ◽  
G. Bellusci ◽  
N. M. Myres ◽  
...  

2014 ◽  
Vol 514 ◽  
pp. 217-229 ◽  
Author(s):  
HY Wang ◽  
LW Botsford ◽  
JW White ◽  
MJ Fogarty ◽  
F Juanes ◽  
...  

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