Genome-wide association studies for growth traits in buffaloes using the single step genomic BLUP

2019 ◽  
Vol 61 (1) ◽  
pp. 113-115 ◽  
Author(s):  
Francisco Ribeiro de Araujo Neto ◽  
Daniel Jordan de Abreu Santos ◽  
Gerardo Alves Fernandes Júnior ◽  
Rusbel Raul Aspilcueta-Borquis ◽  
André Vieira do Nascimento ◽  
...  
2021 ◽  
Vol 12 ◽  
Author(s):  
Yonglan Liao ◽  
Zhicheng Wang ◽  
Leonardo S. Glória ◽  
Kai Zhang ◽  
Cuixia Zhang ◽  
...  

Growth is a complex trait with moderate to high heritability in livestock and must be described by the longitudinal data measured over multiple time points. Therefore, the used phenotype in genome-wide association studies (GWAS) of growth traits could be either the measures at the preselected time point or the fitted parameters of whole growth trajectory. A promising alternative approach was recently proposed that combined the fitting of growth curves and estimation of single-nucleotide polymorphism (SNP) effects into single-step nonlinear mixed model (NMM). In this study, we collected the body weights at 35, 42, 49, 56, 63, 70, and 84 days of age for 401 animals in a crossbred population of meat rabbits and compared five fitting models of growth curves (Logistic, Gompertz, Brody, Von Bertalanffy, and Richards). The logistic model was preferably selected and subjected to GWAS using the approach of single-step NMM, which was based on 87,704 genome-wide SNPs. A total of 45 significant SNPs distributed on five chromosomes were found to simultaneously affect the two growth parameters of mature weight (A) and maturity rate (K). However, no SNP was found to be independently associated with either A or K. Seven positional genes, including KCNIP4, GBA3, PPARGC1A, LDB2, SHISA3, GNA13, and FGF10, were suggested to be candidates affecting growth performances in meat rabbits. To the best of our knowledge, this is the first report of GWAS based on single-step NMM for longitudinal traits in rabbits, which also revealed the genetic architecture of growth traits that are helpful in implementing genome selection.


2011 ◽  
Vol 89 (6) ◽  
pp. 1684-1697 ◽  
Author(s):  
S. Bolormaa ◽  
B. J. Hayes ◽  
K. Savin ◽  
R. Hawken ◽  
W. Barendse ◽  
...  

2019 ◽  
Author(s):  
M. Pérez-Enciso ◽  
L. C. Ramírez-Ayala ◽  
L.M. Zingaretti

AbstractBackgroundGenomic Prediction (GP) is the procedure whereby molecular information is used to predict complex phenotypes. Although GP can significantly enhance predictive accuracy, it can be expensive and difficult to implement. To help in designing optimum experiments, including genome wide association studies and genomic selection experiments, we have developed SeqBreed, a generic and flexible python3 forward simulator.ResultsSeqBreed accommodates sex and mitochondrion chromosomes as well as autopolyploidy. It can simulate any number of complex phenotypes determined by any number of causal loci. SeqBreed implements several GP methods, including single step GBLUP. We demonstrate its functionality with Drosophila Genome Reference Panel (DGRP) sequence data and with tetraploid potato genotypes.ConclusionsSeqBreed is a flexible and easy to use tool appropriate for optimizing GP or genome wide association studies. It incorporates some of the most popular GP methods and includes several visualization tools. Code is open and can be freely modified. Software, documentation and examples are available at https://github.com/miguelperezenciso/SeqBreed.


2020 ◽  
Vol 103 (11) ◽  
pp. 10347-10360
Author(s):  
Pamela I. Otto ◽  
Simone E.F. Guimarães ◽  
Mario P.L. Calus ◽  
Jeremie Vandenplas ◽  
Marco A. Machado ◽  
...  

2020 ◽  
Vol 99 (5) ◽  
pp. 2349-2361 ◽  
Author(s):  
Hui Zhang ◽  
Lin-Yong Shen ◽  
Zi-Chun Xu ◽  
Luke M. Kramer ◽  
Jia-Qiang Yu ◽  
...  

2022 ◽  
Vol 23 (1) ◽  
Author(s):  
Dachang Dou ◽  
Linyong Shen ◽  
Jiamei Zhou ◽  
Zhiping Cao ◽  
Peng Luan ◽  
...  

Abstract Background The identification of markers and genes for growth traits may not only benefit for marker assist selection /genomic selection but also provide important information for understanding the genetic foundation of growth traits in broilers. Results In the current study, we estimated the genetic parameters of eight growth traits in broilers and carried out the genome-wide association studies for these growth traits. A total of 113 QTNs discovered by multiple methods together, and some genes, including ACTA1, IGF2BP1, TAPT1, LDB2, PRKCA, TGFBR2, GLI3, SLC16A7, INHBA, BAMBI, APCDD1, GPR39, and GATA4, were identified as important candidate genes for rapid growth in broilers. Conclusions The results of this study will provide important information for understanding the genetic foundation of growth traits in broilers.


2019 ◽  
Author(s):  
Ignacio Aguilar ◽  
Andres Legarra ◽  
Fernando Cardoso ◽  
Yutaka Masuda ◽  
Daniela Lourenco ◽  
...  

ABSTRACTBACKGROUNDSingle Step GBLUP (SSGBLUP) is the most comprehensive method for genomic prediction. Point estimates of marker effects from SSGBLUP are often used for Genome Wide Association Studies (GWAS) without a formal framework of hypothesis testing. Our objective was to implement p-values for GWAS studies in the ssGBLUP framework, showing algorithms, computational procedures, and an application to a large beef cattle population.METHODSP-values were obtained based on the prediction error (co)variance for SNP, which uses the inverse of the coefficient matrix and formulas to compute SNP effects.RESULTSComputation of p-values took a negligible time for a dataset with almost 2 million animals in the pedigree and 1424 genotyped sires, and no inflation was observed. The SNP passing the Bonferroni threshold of 5.9 in the −log10 scale were the same as those that explained the highest proportion of additive genetic variance, but the latter was penalized (as GWAS signal) by low allele frequency.CONCLUSIONThe exact p-value for SSGWAS is a very general and efficient strategy for QTL detection and testing. It can be used in complex data sets such as used in animal breeding, where only a proportion of pedigreed animals are genotyped.


2017 ◽  
Author(s):  
Yan Zhang ◽  
Guanghao Qi ◽  
Ju-Hyun Park ◽  
Nilanjan Chatterjee

AbstractSummary-level statistics from genome-wide association studies are now widely used to estimate heritability and co-heritability of traits using the popular linkage-disequilibrium-score (LD-score) regression method. We develop a likelihood-based approach for analyzing summary-level statistics and external LD information to estimate common variants effect-size distributions, characterized by proportion of underlying susceptibility SNPs and a flexible normal-mixture model for their effects. Analysis of summary-level results across 32 GWAS reveals that while all traits are highly polygenic, there is wide diversity in the degrees of polygenicity. The effect-size distributions for susceptibility SNPs could be adequately modeled by a single normal distribution for traits related to mental health and ability and by a mixture of two normal distributions for all other traits. Among quantitative traits, we predict the sample sizes needed to identify SNPs which explain 80% of GWAS heritability to be between 300K-500K for some of the early growth traits, between 1-2 million for some anthropometric and cholesterol traits and multiple millions for body mass index and some others. The corresponding predictions for disease traits are between 200K-400K for inflammatory bowel diseases, close to one million for a variety of adult onset chronic diseases and between 1-2 million for psychiatric diseases.


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