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Deleted copy number variation of Hanwoo and Holstein using next generation sequencing at the population level

Overview of attention for article published in BMC Genomics, March 2014
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  • Above-average Attention Score compared to outputs of the same age and source (60th percentile)

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56 Mendeley
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Title
Deleted copy number variation of Hanwoo and Holstein using next generation sequencing at the population level
Published in
BMC Genomics, March 2014
DOI 10.1186/1471-2164-15-240
Pubmed ID
Authors

Dong-Hyun Shin, Hyun-Jeong Lee, Seoae Cho, Hyeon Jeong Kim, Jae Yeon Hwang, Chang-Kyu Lee, JinYoung Jeong, Duhak Yoon, Heebal Kim

Abstract

Copy number variation (CNV), a source of genetic diversity in mammals, has been shown to underlie biological functions related to production traits. Notwithstanding, there have been few studies conducted on CNVs using next generation sequencing at the population level.

X Demographics

X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 56 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Brazil 2 4%
Uruguay 1 2%
Canada 1 2%
France 1 2%
Unknown 51 91%

Demographic breakdown

Readers by professional status Count As %
Researcher 12 21%
Student > Ph. D. Student 10 18%
Student > Master 10 18%
Student > Doctoral Student 6 11%
Student > Bachelor 6 11%
Other 2 4%
Unknown 10 18%
Readers by discipline Count As %
Agricultural and Biological Sciences 34 61%
Biochemistry, Genetics and Molecular Biology 6 11%
Veterinary Science and Veterinary Medicine 3 5%
Computer Science 1 2%
Neuroscience 1 2%
Other 0 0%
Unknown 11 20%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 2. 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 05 March 2015.
All research outputs
#13,866,700
of 23,498,099 outputs
Outputs from BMC Genomics
#5,117
of 10,787 outputs
Outputs of similar age
#112,063
of 226,087 outputs
Outputs of similar age from BMC Genomics
#56
of 158 outputs
Altmetric has tracked 23,498,099 research outputs across all sources so far. This one is in the 39th percentile – i.e., 39% of other outputs scored the same or lower than it.
So far Altmetric has tracked 10,787 research outputs from this source. They receive a mean Attention Score of 4.7. This one is in the 49th percentile – i.e., 49% of its peers scored the same or lower than it.
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 226,087 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 48th percentile – i.e., 48% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 158 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 60% of its contemporaries.