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Comparisons of improved genomic predictions generated by different imputation methods for genotyping by sequencing data in livestock populations

机译:通过牲畜群体测序数据进行基因分型产生改进的基因组预测的比较

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摘要

Background:Genotyping by sequencing(GBS)still has problems with missing genotypes.Imputation is important for using GBS for genomic predictions,especially for low depths,due to the large number of missing genotypes.Minor allele frequency(MAF)is widely used as a marker data editing criteria for genomic predictions.In this study,three imputation methods(Beagle,IMPUTE2 and FImpute software)based on four MAF editing criteria were investigated with regard to imputation accuracy of missing genotypes and accuracy of genomic predictions,based on simulated data of livestock population.Results:Four MAFs(no MAF limit,MAF≥0.001,MAF≥0.01 and MAF≥0.03)were used for editing marker data before imputation.Beagle,IMPUTE2 and FImpute software were applied to impute the original GBS.Additionally,IMPUTE2 also imputed the expected genotype dosage after genotype correction(GcIM).The reliability of genomic predictions was calculated using GBS and imputed GBS data.The results showed that imputation accuracies were the same for the three imputation methods,except for the data of sequencing read depth(depth)=2,where FImpute had a slightly lower imputation accuracy than Beagle and IMPUTE2.GcIM was observed to be the best for all of the imputations at depth=4,5 and 10,but the worst for depth=2.For genomic prediction,retaining more SNPs with no MAF limit resulted in higher reliability.As the depth increased to 10,the prediction reliabilities approached those using true genotypes in the GBS loci.Beagle and IMPUTE2 had the largest increases in prediction reliability of 5 percentage points,and FImpute gained 3 percentage points at depth=2.The best prediction was observed at depth=4,5 and 10 using GcIM,but the worst prediction was also observed using GcIM at depth=2.Conclusions:The current study showed that imputation accuracies were relatively low for GBS with low depths and high for GBS with high depths.Imputation resulted in larger gains in the reliability of genomic predictions for GBS with lower depths.These results suggest that the application of IMPUTE2,based on a corrected GBS(GcIM)to improve genomic predictions for higher depths,and FImpute software could be a good alternative for routine imputation.
机译:背景:通过测序(GBS)的基因分型仍然存在缺失基因型的问题。由于大量缺失的基因型,截瘫对基因组预测的截瘫是重要的,特别是对于低深度,因此缺失的基因型。等位基因频率(MAF)被广泛用作基因组预测的标记数据编辑标准。根据模拟数据,研究了基于四个MAF编辑标准的基于四个MAF编辑标准的三个撤销方法(Beaggle,Impute2和Fimpute软件)研究了基于模拟数据牲畜人口。结果:四个MAF(无MAF限制,MAF≥0.001,MAF≥0.01和MAF≥0.03)用于编辑标记数据之前。编辑,应用赋予赋予释放的软件,以赋予原始GBS.Aditionally,Impute2还在基因型校正(GCIM)之后占据了预期的基因型剂量。使用GBS计算基因组预测的可靠性,并且避阻GBS数据计算。结果表明归属于估算精度对于三种估算方法是相同的,除了测序读取深度(深度)= 2的数据外,其中Fimpute具有略低的估计精度,并且被观察到为所有避免的避难所都是最佳的= 4,5和10,但深度最差= 2.对于基因组预测,保持更多的SNP,没有MAF限制导致更高的可靠性导致。增加到10,预测可靠性在GBS基因座中使用真实基因型接近那些.beagle和赋予舒适的预测可靠性增加了5个百分点的预测可靠性增加,并且在深度下获得了3个百分点= 2.使用GCIM在深度= 4,5和10时观察到最佳预测,但也观察到最坏的预测使用GCIM深度= 2.结论:目前的研究表明,对于具有高深的GBS的GBS具有低深度和高度高度的GBS的载口均匀性。截瘫导致GB的基因组预测的可靠性导致GB的可靠性较大r深度。结果表明,基于校正的GBS(GCIM)来改善更高深度的基因组预测,并且Fimpute软件的应用可能是常规估算的替代方案。

著录项

  • 来源
    《畜牧与生物技术杂志:英文版》 |2020年第002期|P.316-326|共11页
  • 作者单位

    Quantitative Genomics Bioinformatics and Computational Biology Group Department of Applied Mathematics and Computer Science Technical University of Denmark Richard Peterson Plads Building 324 2800 Kongens Lyngby DenmarkCenter for Quantitative Genetics and Genomics Department of Molecular Biology and Genetics Aarhus University 8830 Tjele Denmark;

    Center for Quantitative Genetics and Genomics Department of Molecular Biology and Genetics Aarhus University 8830 Tjele Denmark;

    Quantitative Genomics Bioinformatics and Computational Biology Group Department of Applied Mathematics and Computer Science Technical University of Denmark Richard Peterson Plads Building 324 2800 Kongens Lyngby DenmarkDepartment of Molecular Biology and Genetics Aarhus University 8000 Aarhus C DenmarkCollege of Animal Science and Technology Northwest A&F University Yangling 712100 Shannxi China;

    Center for Quantitative Genetics and Genomics Department of Molecular Biology and Genetics Aarhus University 8830 Tjele Denmark;

    Quantitative Genomics Bioinformatics and Computational Biology Group Department of Applied Mathematics and Computer Science Technical University of Denmark Richard Peterson Plads Building 324 2800 Kongens Lyngby Denmark;

  • 收录信息 中国科学引文数据库(CSCD);
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 神经病学与精神病学;
  • 关键词

    Genomic prediction; Genotyping by sequencing; Imputation; MAF; Simulation;

    机译:基因组预测;测序的基因分型;归责;MAF;模拟;
  • 入库时间 2022-08-19 04:48:55
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