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Inconsistency and features of single nucleotide variants detected in whole exome sequencing versus transcriptome sequencing: A case study in lung cancer

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Year: 2015
Type: article
Source: Methods
DOI: 10.1016/j.ymeth.2015.04.016
Authors: Timothy D. O’Brien, Peilin Jia, Junfeng Xia, Uma Saxena, Hailing Jin, Huy Vuong, Pora Kim, Qingguo Wang, Martin J. Aryee, Mari Mino-Kenudson, Jeffrey A. Engelman, Long P. Le, A. John Iafrate, Rebecca S. Heist, William Pao, Zhongming Zhao
Institutions: Vanderbilt University, Massachusetts General Hospital, Vanderbilt University Medical Center, Harvard University
Language: English

Topic: Genomics and Rare Diseases
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: LUNGevity Foundation, Vanderbilt University, National Institutes of Health, National Cancer Institute, National Institute of General Medical Sciences, U.S. National Library of Medicine
Awards: Mapping the Genetic Architecture of Complex Disease via RNA-seq and GWAS, SPORE in GI Cancer, Training Program on Genetic Variation and Human Phenotypes, SPORE in Breast Cancer, Cancer Center Support Grant
OpenAlex ID: W1973489592
FWCI: 3.65
Cites: 34
Cited by: 43
Related to: 10
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