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Publications
マクロジェングループの研究開発論文です。
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2018年 Cancer Immunol Res. (2018 Jul; 6(7), 848-859.)
Whole exome and transcriptome analyses integrated with microenvironmental immune signatures of lung squamous cell carcinoma.
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2017年 Nature Genetics. (2017 May; 49(7), 1082-1088.)
Whole-genome resequencing of 292 pigeonpea accessions identifies genomic regions associated with domestication and agronomic traits.
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2017年 PLoS One. (2017 Apr; 12(4), e0176462.)
Altered nucleocytoplasmic proteome and transcriptome distributions in an in vitro model of amyotrophic lateral sclerosis.
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2016年 Nature. (2016 Oct; 538, 243-247.)
De novo assembly and phasing of a Korean human genome.
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2016年 Oncotarget. (2016 Mar; 7(9), 10547-10556.)
Next-generation sequencing reveals somatic mutations that confer exceptional response to everolimus.
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2015年 PLoS One. (2015 Oct; 10(10), e0139716.)
Family-Based Association Study of Pulmonary Function in a Population in Northeast Asia.
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2015年 Nat Med. (2015 Apr; 21(4), 395-400.)
Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy.
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2014年 Nat Commun. (2014 Dec; 5, 5619.)
An epigenomic roadmap to induced pluripotency reveals DNA methylation as a reprogramming modulator.
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2014年 Nature. (2014 Dec; 516(7530), 192-197.)
Divergent reprogramming routes lead to alternative stem-cell states.
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2014年 Nature. (2014 Dec; 516(7530), 198-206.)
Genome-wide characterization of the routes to pluripotency.
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2013年 PLoS One. (2013 Dec; 8(12), e81975.)
Predictive efficacy of low burden EGFR mutation detected by next-generation sequencing on response to EGFR tyrosine kinase inhibitors in non-small-cell lung carcinoma.
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2012年 Genome Research(2012 Nov;22(11),2109-19)
The transcriptional landscape and mutational profile of lung adenocarcinoma
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2012年 Genome Research(2012 Mar; 22(3),436-45)
A transforming KIF5B and RET gene fusion in lung adenocarcinoma revealed from whole-genome and transcriptome sequencing
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2011年 Nature Genetics(2011 July;43,745-752)
Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals
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2010年 Nature Genetics(Nat. Genet 2010 May;42(5), 400-5)
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
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2009年 Nature(Nature, 2009 Aug 20;460(7258) 1011-5
A highly annotated whole-genome sequence of a Korean individual
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