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CNV-seq, a new method to detect copy number variation using high-throughput sequencing

Overview of attention for article published in BMC Bioinformatics, March 2009
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (92nd percentile)
  • High Attention Score compared to outputs of the same age and source (94th percentile)

Mentioned by

patent
36 patents
wikipedia
2 Wikipedia pages
q&a
1 Q&A thread

Citations

dimensions_citation
500 Dimensions

Readers on

mendeley
752 Mendeley
citeulike
47 CiteULike
connotea
11 Connotea
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Title
CNV-seq, a new method to detect copy number variation using high-throughput sequencing
Published in
BMC Bioinformatics, March 2009
DOI 10.1186/1471-2105-10-80
Pubmed ID
Authors

Chao Xie, Martti T Tammi

Abstract

DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 752 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 29 4%
United Kingdom 13 2%
Brazil 9 1%
Germany 8 1%
France 6 <1%
Belgium 4 <1%
Netherlands 4 <1%
Italy 3 <1%
Switzerland 3 <1%
Other 15 2%
Unknown 658 88%

Demographic breakdown

Readers by professional status Count As %
Researcher 223 30%
Student > Ph. D. Student 162 22%
Student > Master 73 10%
Student > Bachelor 48 6%
Professor > Associate Professor 42 6%
Other 121 16%
Unknown 83 11%
Readers by discipline Count As %
Agricultural and Biological Sciences 416 55%
Biochemistry, Genetics and Molecular Biology 119 16%
Computer Science 43 6%
Medicine and Dentistry 40 5%
Mathematics 10 1%
Other 31 4%
Unknown 93 12%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 15. 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 03 October 2023.
All research outputs
#2,171,700
of 23,575,346 outputs
Outputs from BMC Bioinformatics
#556
of 7,398 outputs
Outputs of similar age
#6,728
of 95,068 outputs
Outputs of similar age from BMC Bioinformatics
#3
of 50 outputs
Altmetric has tracked 23,575,346 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 90th percentile: it's in the top 10% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 7,398 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 5.4. This one has done particularly well, scoring higher than 92% 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 95,068 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 92% of its contemporaries.
We're also able to compare this research output to 50 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 94% of its contemporaries.