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Statistical aspects of discerning indel-type structural variation via DNA sequence alignment

Overview of attention for article published in BMC Genomics, August 2009
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3 Wikipedia pages

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Title
Statistical aspects of discerning indel-type structural variation via DNA sequence alignment
Published in
BMC Genomics, August 2009
DOI 10.1186/1471-2164-10-359
Pubmed ID
Authors

Michael C Wendl, Richard K Wilson

Abstract

Structural variations in the form of DNA insertions and deletions are an important aspect of human genetics and especially relevant to medical disorders. Investigations have shown that such events can be detected via tell-tale discrepancies in the aligned lengths of paired-end DNA sequencing reads. Quantitative aspects underlying this method remain poorly understood, despite its importance and conceptual simplicity. We report the statistical theory characterizing the length-discrepancy scheme for Gaussian libraries, including coverage-related effects that preceding models are unable to account for.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 40 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 5%
Germany 1 3%
Brazil 1 3%
Unknown 36 90%

Demographic breakdown

Readers by professional status Count As %
Researcher 17 43%
Student > Ph. D. Student 10 25%
Professor > Associate Professor 3 8%
Student > Bachelor 2 5%
Student > Master 2 5%
Other 4 10%
Unknown 2 5%
Readers by discipline Count As %
Agricultural and Biological Sciences 22 55%
Mathematics 3 8%
Computer Science 3 8%
Biochemistry, Genetics and Molecular Biology 2 5%
Engineering 2 5%
Other 5 13%
Unknown 3 8%
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 07 November 2020.
All research outputs
#8,535,472
of 25,374,647 outputs
Outputs from BMC Genomics
#3,907
of 11,244 outputs
Outputs of similar age
#42,144
of 123,272 outputs
Outputs of similar age from BMC Genomics
#30
of 62 outputs
Altmetric has tracked 25,374,647 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 11,244 research outputs from this source. They receive a mean Attention Score of 4.8. This one has gotten more attention than average, scoring higher than 58% 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 123,272 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 18th percentile – i.e., 18% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 62 others from the same source and published within six weeks on either side of this one. This one is in the 12th percentile – i.e., 12% of its contemporaries scored the same or lower than it.