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Application of imputation methods to genomic selection in Chinese Holstein cattle

DOI: 10.1186/2049-1891-3-6

Keywords: Chinese Holstein Cows, dairy cattle, genomic selection, imputation methods, quality control, SNP

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Abstract:

Genomic selection is becoming prevalent and practicable in dairy cattle breeding, where genomic breeding values of animals are estimated using high density single nucleotide polymorphisms (SNPs) and are the basis for the selection of elite animals [1]. Genomic selection combines information on genotypes, phenotypes and pedigree to increase the accuracy of the estimated breeding values (EVBs). Low-, medium- and high-density platforms have become available and this new technology has revolutionized dairy cattle breeding and has led to an extraordinary amount of research activity [2-4]. Tens of thousands of dairy cattle have been genotyped using the BovineSNP50 BeadChip (Illumina Inc. San Diego, CA) or related platforms, and the resulting genomic data have been evaluated [5]http://www.interbull.org/ webcite. Genomic estimated breeding values (GEBVs) are at the core of genomic selection. The GEBV is calculated as the sum of all SNP effects; the estimation of SNP effects therefore plays an important role in genomic selection. In the SNP genotype data obtained from the SNP chip technique, missing genotype information is a common phenomenon that leads to a low call rate for some SNPs and for some animals. The routine data quality control procedure in genomic selection eliminates SNPs and animals with low call rates from the data sets, resulting in the loss of information and a decrease in the accuracy of the GEBV. Imputation can be used to deduce the missing genotypes and could be helpful in increasing the accuracy of genomic selection. Imputation also allows for the use of low-density chips that may be more cost-effective, facilitating the widespread implementation of whole-genome selection [5,6].Several imputation methods have been proposed and are implemented in programs like fastPHASE [7], Beagle [8], and findhap [9]. These methods impute the missing genotypes based on reconstructed haplotypes informed by linkage disequilibrium between SNPs. They all use different meth

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