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PennCNV in whole-genome sequencing data

Overview of attention for article published in BMC Bioinformatics, October 2017
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • Good Attention Score compared to outputs of the same age (72nd percentile)
  • Good Attention Score compared to outputs of the same age and source (73rd percentile)

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1 policy source
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Citations

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44 Mendeley
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Title
PennCNV in whole-genome sequencing data
Published in
BMC Bioinformatics, October 2017
DOI 10.1186/s12859-017-1802-x
Pubmed ID
Authors

Leandro de Araújo Lima, Kai Wang

Abstract

The use of high-throughput sequencing data has improved the results of genomic analysis due to the resolution of mapping algorithms. Although several tools for copy-number variation calling in whole genome sequencing have been published, the noisy nature of sequencing data is still a limitation for accuracy and concordance among such tools. To assess the performance of PennCNV original algorithm for array data in whole genome sequencing data, we processed mapping (BAM) files to extract coverage, representing log R ratio (LRR) of signal intensity, and B allele frequency (BAF). We used high quality sample NA12878 from the recently reported NIST database and created 10 artificial samples with several CNVs spread along all chromosomes. We compared PennCNV-Seq with other tools with general deletions and duplications, as well as for different number of copies and copy-neutral loss-of-heterozygosity (LOH). PennCNV-Seq was able to find correct CNVs and can be integrated in existing CNV calling pipelines to report accurately the number of copies in specific genomic regions.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 44 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 44 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 10 23%
Student > Postgraduate 6 14%
Student > Master 5 11%
Student > Ph. D. Student 5 11%
Student > Doctoral Student 2 5%
Other 7 16%
Unknown 9 20%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 18 41%
Agricultural and Biological Sciences 8 18%
Neuroscience 3 7%
Medicine and Dentistry 3 7%
Unspecified 1 2%
Other 1 2%
Unknown 10 23%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 6. 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 22 October 2019.
All research outputs
#5,561,728
of 25,779,988 outputs
Outputs from BMC Bioinformatics
#1,956
of 7,745 outputs
Outputs of similar age
#88,590
of 332,771 outputs
Outputs of similar age from BMC Bioinformatics
#28
of 105 outputs
Altmetric has tracked 25,779,988 research outputs across all sources so far. Compared to these this one has done well and is in the 75th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 7,745 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 5.5. This one has gotten more attention than average, scoring higher than 73% 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 332,771 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 72% of its contemporaries.
We're also able to compare this research output to 105 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 73% of its contemporaries.