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An improved approach for accurate and efficient calling of structural variations with low-coverage sequence data

Overview of attention for article published in BMC Bioinformatics, April 2012
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Title
An improved approach for accurate and efficient calling of structural variations with low-coverage sequence data
Published in
BMC Bioinformatics, April 2012
DOI 10.1186/1471-2105-13-s6-s6
Pubmed ID
Authors

Jin Zhang, Jiayin Wang, Yufeng Wu

Abstract

Recent advances in sequencing technologies make it possible to comprehensively study structural variations (SVs) using sequence data of large-scale populations. Currently, more efforts have been taken to develop methods that call SVs with exact breakpoints. Among these approaches, split-read mapping methods can be applied on low-coverage sequence data. With increasing amount of data generated, more efficient split-read mapping methods are still needed. Also, since sequence errors can not be avoided for the current sequencing technologies, more accurate split-read mapping methods are still needed to better handle sequence errors.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 78 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 1 1%
Italy 1 1%
Brazil 1 1%
Unknown 75 96%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 25 32%
Researcher 13 17%
Student > Master 12 15%
Student > Doctoral Student 4 5%
Student > Bachelor 4 5%
Other 7 9%
Unknown 13 17%
Readers by discipline Count As %
Agricultural and Biological Sciences 25 32%
Biochemistry, Genetics and Molecular Biology 17 22%
Computer Science 14 18%
Neuroscience 2 3%
Medicine and Dentistry 2 3%
Other 5 6%
Unknown 13 17%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. 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 29 October 2012.
All research outputs
#16,770,898
of 24,666,614 outputs
Outputs from BMC Bioinformatics
#5,560
of 7,565 outputs
Outputs of similar age
#107,652
of 165,909 outputs
Outputs of similar age from BMC Bioinformatics
#65
of 93 outputs
Altmetric has tracked 24,666,614 research outputs across all sources so far. This one is in the 21st percentile – i.e., 21% of other outputs scored the same or lower than it.
So far Altmetric has tracked 7,565 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 5.5. This one is in the 18th percentile – i.e., 18% of its peers scored the same or lower than it.
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We're also able to compare this research output to 93 others from the same source and published within six weeks on either side of this one. This one is in the 16th percentile – i.e., 16% of its contemporaries scored the same or lower than it.