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inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing

Overview of attention for article published in Evolutionary Bioinformatics, September 2020
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Citations

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Title
inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing
Published in
Evolutionary Bioinformatics, September 2020
DOI 10.1177/1176934320956577
Pubmed ID
Authors

Saowwapark Chanwigoon, Sakkayaphab Piwluang, Duangdao Wichadakul

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 22 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 22 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 23%
Other 3 14%
Student > Master 3 14%
Student > Ph. D. Student 3 14%
Student > Bachelor 2 9%
Other 2 9%
Unknown 4 18%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 9 41%
Agricultural and Biological Sciences 2 9%
Medicine and Dentistry 2 9%
Nursing and Health Professions 1 5%
Veterinary Science and Veterinary Medicine 1 5%
Other 1 5%
Unknown 6 27%