PhenoSpD: an integrated toolkit for phenotypic correlation estimation and multiple testing correction using GWAS summary statistics.

Zheng, Jie; Richardson, Tom G; Millard, Louise A C; Hemani, Gibran; Elsworth, Benjamin L; Raistrick, Christopher A; Vilhjalmsson, Bjarni; Neale, Benjamin M; Haycock, Philip C; Smith, George Davey; Gaunt, Tom R

Zheng, Jie; Richardson, Tom G; Millard, Louise A C; Hemani, Gibran; Elsworth, Benjamin L; Raistrick, Christopher A; Vilhjalmsson, Bjarni; Neale, Benjamin M; Haycock, Philip C; Smith, George Davey; Gaunt, Tom R.

Afiliação

Zheng J; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, BS8 2BN, UK.
Richardson TG; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, BS8 2BN, UK.
Millard LAC; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, BS8 2BN, UK.
Hemani G; Intelligent Systems Laboratory, University of Bristol, Tyndall Ave, Bristol, BS8 1TH, UK.
Elsworth BL; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, BS8 2BN, UK.
Raistrick CA; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, BS8 2BN, UK.
Vilhjalmsson B; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, BS8 2BN, UK.
Neale BM; Åarhus Center for Bioinformatics BIRC, Aarhus University, Nordre Ringgade, 1,8000, Aarhus C, Denmark.
Haycock PC; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, 415 Main St, Cambridge, MA, 02142, USA.
Smith GD; Analytical and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.
Gaunt TR; MRC Integrative Epidemiology Unit, University of Bristol, Oakfield House, Bristol, BS8 2BN, UK.

Gigascience ; 7(8)2018 08 01.

Article em En | MEDLINE | ID: mdl-30165448

Assuntos

Estudo de Associação Genômica Ampla/métodos; Polimorfismo de Nucleotídeo Único; Software; Humanos; Desequilíbrio de Ligação; Modelos Genéticos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Software / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Gigascience Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido

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