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Identification of Sequence Variants in Genetic Disease-Causing Genes Using Targeted Next-Generation Sequencing

Overview of attention for article published in PLOS ONE, December 2011
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Title
Identification of Sequence Variants in Genetic Disease-Causing Genes Using Targeted Next-Generation Sequencing
Published in
PLOS ONE, December 2011
DOI 10.1371/journal.pone.0029500
Pubmed ID
Authors

Xiaoming Wei, Xiangchun Ju, Xin Yi, Qian Zhu, Ning Qu, Tengfei Liu, Yang Chen, Hui Jiang, Guanghui Yang, Ruan Zhen, Zhangzhang Lan, Ming Qi, Jinming Wang, Yi Yang, Yuxing Chu, Xiaoyan Li, Yanfang Guang, Jian Huang

Abstract

Identification of gene variants plays an important role in research on and diagnosis of genetic diseases. A combination of enrichment of targeted genes and next-generation sequencing (targeted DNA-HiSeq) results in both high efficiency and low cost for targeted sequencing of genes of interest.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 116 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Korea, Republic of 2 2%
France 1 <1%
Australia 1 <1%
Brazil 1 <1%
Sweden 1 <1%
United Kingdom 1 <1%
Denmark 1 <1%
United States 1 <1%
Unknown 107 92%

Demographic breakdown

Readers by professional status Count As %
Researcher 29 25%
Student > Ph. D. Student 16 14%
Student > Master 11 9%
Student > Bachelor 10 9%
Other 8 7%
Other 19 16%
Unknown 23 20%
Readers by discipline Count As %
Agricultural and Biological Sciences 44 38%
Biochemistry, Genetics and Molecular Biology 15 13%
Medicine and Dentistry 15 13%
Neuroscience 3 3%
Computer Science 3 3%
Other 9 8%
Unknown 27 23%