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1.
J Anim Sci Biotechnol ; 14(1): 119, 2023 Sep 09.
Artigo em Inglês | MEDLINE | ID: mdl-37684681

RESUMO

BACKGROUND: Many phenotypes in animal breeding are derived from incomplete measures, especially if they are challenging or expensive to measure precisely. Examples include time-dependent traits such as reproductive status, or lifespan. Incomplete measures for these traits result in phenotypes that are subject to left-, interval- and right-censoring, where phenotypes are only known to fall below an upper bound, between a lower and upper bound, or above a lower bound respectively. Here we compare three methods for deriving phenotypes from incomplete data using age at first elevation (> 1 ng/mL) in blood plasma progesterone (AGEP4), which generally coincides with onset of puberty, as an example trait. METHODS: We produced AGEP4 phenotypes from three blood samples collected at about 30-day intervals from approximately 5,000 Holstein-Friesian or Holstein-Friesian × Jersey cross-bred dairy heifers managed in 54 seasonal-calving, pasture-based herds in New Zealand. We used these actual data to simulate 7 different visit scenarios, increasing the extent of censoring by disregarding data from one or two of the three visits. Three methods for deriving phenotypes from these data were explored: 1) ordinal categorical variables which were analysed using categorical threshold analysis; 2) continuous variables, with a penalty of 31 d assigned to right-censored phenotypes; and 3) continuous variables, sampled from within a lower and upper bound using a data augmentation approach. RESULTS: Credibility intervals for heritability estimations overlapped across all methods and visit scenarios, but estimated heritabilities tended to be higher when left censoring was reduced. For sires with at least 5 daughters, the correlations between estimated breeding values (EBVs) from our three-visit scenario and each reduced data scenario varied by method, ranging from 0.65 to 0.95. The estimated breed effects also varied by method, but breed differences were smaller as phenotype censoring increased. CONCLUSION: Our results indicate that using some methods, phenotypes derived from one observation per offspring for a time-dependent trait such as AGEP4 may provide comparable sire rankings to three observations per offspring. This has implications for the design of large-scale phenotyping initiatives where animal breeders aim to estimate variance parameters and estimated breeding values (EBVs) for phenotypes that are challenging to measure or prohibitively expensive.

2.
Front Genet ; 13: 867152, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35957692

RESUMO

Time-dependent traits are often subject to censorship, where instead of precise phenotypes, only a lower and/or upper bound can be established for some of the individuals. Censorship reduces the precision of phenotypes but can represent compromise between measurement cost and animal ethics considerations. This compromise is particularly relevant for genetic evaluation because phenotyping initiatives often involve thousands of individuals. This research aimed to: 1) demonstrate a data augmentation approach for analysing censored phenotypes, and 2) quantify the implications of phenotype censorship on estimation of heritabilities and predictions of breeding values. First, we simulated uncensored phenotypes, representing fine-scale "age at puberty" for each individual in a population of some 5,000 animals across 50 herds. Analysis of these uncensored phenotypes provided a gold-standard control. We then produced seven "test" phenotypes by superimposing varying degrees of left, interval, and/or right censorship, as if herds were measured on only one, two or three occasions, with a binary measure categorized for animals at each visit (either pre or post pubertal). We demonstrated that our estimates of heritabilities and predictions of breeding values obtained using a data augmentation approach were remarkably robust to phenotype censorship. Our results have important practical implications for measuring time-dependent traits for genetic evaluation. More specifically, we suggest that data collection can be designed with relatively infrequent repeated measures, thereby reducing costs and increasing feasibility across large numbers of animals.

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