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Identifying individual risk rare variants using protein structure guided local tests (POINT).
Marceau West, Rachel; Lu, Wenbin; Rotroff, Daniel M; Kuenemann, Melaine A; Chang, Sheng-Mao; Wu, Michael C; Wagner, Michael J; Buse, John B; Motsinger-Reif, Alison A; Fourches, Denis; Tzeng, Jung-Ying.
Afiliação
  • Marceau West R; Department of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
  • Lu W; Department of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
  • Rotroff DM; Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, United States of America.
  • Kuenemann MA; Bioinformatics Research Center, North Carolina State University, Raleigh, North Carolina, United States of America.
  • Chang SM; Department of Statistics, National Cheng-Kung University, Tainan, Taiwan.
  • Wu MC; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Wagner MJ; Center for Pharmacogenomics and Individualized Therapy, University of North Carolina, Chapel Hill, North Carolina, United States of America.
  • Buse JB; Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, United States of America.
  • Motsinger-Reif AA; Department of Statistics, North Carolina State University, Raleigh, North Carolina, United States of America.
  • Fourches D; Bioinformatics Research Center, North Carolina State University, Raleigh, North Carolina, United States of America.
  • Tzeng JY; Bioinformatics Research Center, North Carolina State University, Raleigh, North Carolina, United States of America.
PLoS Comput Biol ; 15(2): e1006722, 2019 02.
Article em En | MEDLINE | ID: mdl-30779729

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article