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Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS

Overview of attention for article published in Bioinformatics, January 2012
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Citations

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62 Dimensions

Readers on

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131 Mendeley
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11 CiteULike
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Title
Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS
Published in
Bioinformatics, January 2012
DOI 10.1093/bioinformatics/bts019
Pubmed ID
Authors

Anne-Katrin Emde, Marcel H. Schulz, David Weese, Ruping Sun, Martin Vingron, Vera M. Kalscheuer, Stefan A. Haas, Knut Reinert

Abstract

The reliable detection of genomic variation in resequencing data is still a major challenge, especially for variants larger than a few base pairs. Sequencing reads crossing boundaries of structural variation carry the potential for their identification, but are difficult to map.

X Demographics

X Demographics

The data shown below were collected from the profiles of 5 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 131 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 10 8%
Netherlands 2 2%
Germany 1 <1%
Australia 1 <1%
Sweden 1 <1%
United Kingdom 1 <1%
France 1 <1%
New Zealand 1 <1%
Canada 1 <1%
Other 2 2%
Unknown 110 84%

Demographic breakdown

Readers by professional status Count As %
Researcher 42 32%
Student > Ph. D. Student 39 30%
Student > Master 10 8%
Professor > Associate Professor 9 7%
Other 8 6%
Other 14 11%
Unknown 9 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 64 49%
Computer Science 23 18%
Biochemistry, Genetics and Molecular Biology 14 11%
Engineering 5 4%
Mathematics 4 3%
Other 9 7%
Unknown 12 9%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. 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 02 May 2014.
All research outputs
#8,534,976
of 25,373,627 outputs
Outputs from Bioinformatics
#6,956
of 12,808 outputs
Outputs of similar age
#73,383
of 248,981 outputs
Outputs of similar age from Bioinformatics
#66
of 138 outputs
Altmetric has tracked 25,373,627 research outputs across all sources so far. This one is in the 43rd percentile – i.e., 43% of other outputs scored the same or lower than it.
So far Altmetric has tracked 12,808 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.0. This one is in the 34th percentile – i.e., 34% 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 248,981 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 39th percentile – i.e., 39% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 138 others from the same source and published within six weeks on either side of this one. This one is in the 49th percentile – i.e., 49% of its contemporaries scored the same or lower than it.