2021
DOI: 10.1016/j.smallrumres.2021.106380
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Comparison of haplotype method using for genomic prediction versus single SNP genotypes in sheep breeding programs

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Cited by 3 publications
(2 citation statements)
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“…It is well-established that DNA-based inheritance enables the transmission of selected phenotypes across generations either without changes in the DNA sequence through epigenetic inheritance [31] or through functional mutations involving changes in only one base pair (single nucleotide polymorphisms-SNP). Through next-generation sequencing, SNP are valuable for detecting genetic variability and genomic prediction in sheep breeding programs [32], developing breed-specific DNA markers for breed identification [33,34], animal productivity [35], parentage assignment [36,37], forensics [38], and prediction of meat quality traits [39][40][41].…”
Section: Discussionmentioning
confidence: 99%
“…It is well-established that DNA-based inheritance enables the transmission of selected phenotypes across generations either without changes in the DNA sequence through epigenetic inheritance [31] or through functional mutations involving changes in only one base pair (single nucleotide polymorphisms-SNP). Through next-generation sequencing, SNP are valuable for detecting genetic variability and genomic prediction in sheep breeding programs [32], developing breed-specific DNA markers for breed identification [33,34], animal productivity [35], parentage assignment [36,37], forensics [38], and prediction of meat quality traits [39][40][41].…”
Section: Discussionmentioning
confidence: 99%
“…The number of SNP markers a haploblock should contain and for which regions of the genome the haploblocks should be defined are needed to be considered when building haplotype blocks. Some methods to define haploblock for GS are simply setting windows with a fixed number of contiguous SNPs ( Hayes et al, 2007 ), a fixed range of base pairs on the genome ( Hess et al, 2017 ; Sharifi et al, 2021 ), and a fixed-length in centimorgans ( Sun et al, 2015 ), collectively termed as fixed-length haploblocks, which are in equal sizes of segments in the genome. Some complicated methods to define haploblock for GS attempt to incorporate the LD pattern across the genome ( Cuyabano et al, 2015a ; Won et al, 2021 ), for example, setting minimum pairwise LD cutoffs to group SNPs into haplotypes, termed variable-length haploblocks, which are in unequal sizes of the segments in the genome and may result in less explanatory variables than fixed-length haploblocks ( Cuyabano et al, 2014 ).…”
Section: Introductionmentioning
confidence: 99%