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Leveraging genetically simple traits to identify small-effect variants for complex phenotypes

Overview of attention for article published in BMC Genomics, November 2016
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  • Good Attention Score compared to outputs of the same age and source (76th percentile)

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2 X users
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1 Wikipedia page

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Title
Leveraging genetically simple traits to identify small-effect variants for complex phenotypes
Published in
BMC Genomics, November 2016
DOI 10.1186/s12864-016-3175-3
Pubmed ID
Authors

K. E. Kemper, M. D. Littlejohn, T. Lopdell, B. J. Hayes, L. E. Bennett, R. P. Williams, X. Q. Xu, P. M. Visscher, M. J. Carrick, M. E. Goddard

Abstract

Polymorphisms underlying complex traits often explain a small part (less than 1 %) of the phenotypic variance (σ(2)P). This makes identification of mutations underling complex traits difficult and usually only a subset of large-effect loci are identified. One approach to identify more loci is to increase sample size of experiments but here we propose an alternative. The aim of this paper is to use secondary phenotypes for genetically simple traits during the QTL discovery phase for complex traits. We demonstrate this approach in a dairy cattle data set where the complex traits were milk production phenotypes (fat, milk and protein yield; fat and protein percentage in milk) measured on thousands of individuals while secondary (potentially genetically simpler) traits are detailed milk composition traits (measurements of individual protein abundance, mineral and sugar concentrations; and gene expression). Quantitative trait loci (QTL) were identified using 11,527 Holstein cattle with milk production records and up to 444 cows with milk composition traits. There were eight regions that contained QTL for both milk production and a composition trait, including four novel regions. One region on BTAU1 affected both milk yield and phosphorous concentration in milk. The QTL interval included the gene SLC37A1, a phosphorous antiporter. The most significant imputed sequence variants in this region explained 0.001 σ(2)P for milk yield, and 0.11 σ(2)P for phosphorus concentration. Since the polymorphisms were non-coding, association mapping for SLC37A1 gene expression was performed using high depth mammary RNAseq data from a separate group of 371 lactating cows. This confirmed a strong eQTL for SLC37A1, with peak association at the same imputed sequence variants that were most significant for phosphorus concentration. Fitting any of these variants as covariables in the association analysis removed the QTL signal for milk production traits. Plausible causative mutations in the casein complex region were also identified using a similar strategy. Milk production traits in dairy cows are typical complex traits where polymorphisms explain only a small portion of the phenotypic variance. However, here we show that these mutations can have larger effects on secondary traits, such as concentrations of minerals, proteins and sugars in the milk, and expression levels of genes in mammary tissue. These larger effects were used to successfully map variants for milk production traits. Genetically simple traits also provide a direct biological link between possible causal mutations and the effect of these mutations on milk production.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 59 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 2%
Unknown 58 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 16 27%
Researcher 12 20%
Student > Master 7 12%
Other 3 5%
Student > Postgraduate 3 5%
Other 5 8%
Unknown 13 22%
Readers by discipline Count As %
Agricultural and Biological Sciences 29 49%
Biochemistry, Genetics and Molecular Biology 8 14%
Veterinary Science and Veterinary Medicine 4 7%
Computer Science 1 2%
Immunology and Microbiology 1 2%
Other 2 3%
Unknown 14 24%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 5. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 14 December 2018.
All research outputs
#6,173,745
of 22,899,952 outputs
Outputs from BMC Genomics
#2,641
of 10,674 outputs
Outputs of similar age
#93,951
of 311,569 outputs
Outputs of similar age from BMC Genomics
#52
of 220 outputs
Altmetric has tracked 22,899,952 research outputs across all sources so far. This one has received more attention than most of these and is in the 72nd percentile.
So far Altmetric has tracked 10,674 research outputs from this source. They receive a mean Attention Score of 4.7. This one has gotten more attention than average, scoring higher than 74% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 311,569 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 69% of its contemporaries.
We're also able to compare this research output to 220 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 76% of its contemporaries.