2022
DOI: 10.3389/fvets.2022.760364
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Genome Wide Scan to Identify Potential Genomic Regions Associated With Milk Protein and Minerals in Vrindavani Cattle

Abstract: In this study, genome-wide association study (GWAS) was conducted for identifying significantly associated genomic regions/SNPs with milk protein and minerals in the 96 taurine-indicine crossbred (Vrindavani) cows using 50K SNP Chip. After quality control, a total of 41,427 SNPs were retained and were further analyzed using a single-SNP additive linear model. Lactation stage, parity, test day milk yield and proportion of exotic inheritance were included as fixed effects in GWAS model. Across all traits, 13 gen… Show more

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Cited by 3 publications
(4 citation statements)
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“…FBRSL1 was significantly associated with milk yield in Chinese Holstein cows based on a GWAS for haplotypes [7]. In another genome-wide scan conducted on a tropically adapted Indian composite crossbred dairy cattle breed (Vrindavani cattle), the CACN gene was significantly associated with milk copper content [8].…”
Section: Discussionmentioning
confidence: 97%
See 1 more Smart Citation
“…FBRSL1 was significantly associated with milk yield in Chinese Holstein cows based on a GWAS for haplotypes [7]. In another genome-wide scan conducted on a tropically adapted Indian composite crossbred dairy cattle breed (Vrindavani cattle), the CACN gene was significantly associated with milk copper content [8].…”
Section: Discussionmentioning
confidence: 97%
“…Furthermore, GWASs also contribute to identifying potential candidate genes associated with economic and resilience traits. Several researchers adopted such methodologies to identify potential candidate genes and signatures of selection [7,8].…”
Section: Introductionmentioning
confidence: 99%
“…where y is an n -vector of reproduction traits, W is a matrix of fixed effects including three principal constituents and the parity effect, x is the SNP genotype, α and β are the corresponding coefficients, u is the random effect, ε is the random error, τ −1 is the variance of residual errors, λ is the ratio between the two variance components, K is the kinship matrix, In is the n × n identity matrix, and MVN n denotes the n -dimensional multivariate normal distribution. Thresholds for Bonferroni-adjusted genome-wide significance and suggestive significance were defined as –log 10 ( p ) = 5.68 (0.05/24,123) and –log 10 ( p ) = 4.38 (1/24,123), respectively ( 27 29 ). We defined the 200 kb regions upstream and downstream of the saliency marker as significant for identifying genes in the Biomart program ( Sus scrofa 10.2 ).…”
Section: Methodsmentioning
confidence: 99%
“…The Q and K matrices were calculated by SNP array data using Tassel software. According to the Bonferroni thresholds of GWAS, we defined p = 0.001 (0.05/50) and p = 0.02 (1/50) as the significance thresholds and suggestive significance thresholds, respectively ( 27 29 ). The significance and suggestive significance HCNVRs were annotated using the BioMart program.…”
Section: Methodsmentioning
confidence: 99%