Reducing the search space for causal genetic variants with VASP.

Field, Matthew A; Cho, Vicky; Cook, Matthew C; Enders, Anselm; Vinuesa, Carola G; Whittle, Belinda; Andrews, T Daniel; Goodnow, Chris C

Field, Matthew A; Cho, Vicky; Cook, Matthew C; Enders, Anselm; Vinuesa, Carola G; Whittle, Belinda; Andrews, T Daniel; Goodnow, Chris C.

Afiliação

Field MA; Department of Immunology, John Curtin School of Medical Research, Australian National University, Canberra City, ACT 2601, Australia.
Cho V; Australian Phenomics Facility, Australian National University, Canberra, ACT 2601, Australia.
Cook MC; Department of Immunology, John Curtin School of Medical Research, Australian National University, Canberra City, ACT 2601, Australia, Department of Immunology, The Canberra Hospital, Canberra, ACT 2605, Australia.
Enders A; Department of Immunology, John Curtin School of Medical Research, Australian National University, Canberra City, ACT 2601, Australia, Rammaciotti Immunisation Genomics Laboratory, John Curtin School of Medical Research, Australian National University, Canberra City, ACT 2601, Australia and.
Vinuesa CG; Department of Immunology, John Curtin School of Medical Research, Australian National University, Canberra City, ACT 2601, Australia.
Whittle B; Australian Phenomics Facility, Australian National University, Canberra, ACT 2601, Australia.
Andrews TD; Department of Immunology, John Curtin School of Medical Research, Australian National University, Canberra City, ACT 2601, Australia.
Goodnow CC; Department of Immunology, John Curtin School of Medical Research, Australian National University, Canberra City, ACT 2601, Australia, Immunogenomics Group, Immunology Research Program, Garvan Institute of Medical Research, Darlinghurst, NSW 2010, Australia.

Bioinformatics ; 31(14): 2377-9, 2015 Jul 15.

Article em En | MEDLINE | ID: mdl-25755272

Assuntos

Ligação Genética; Predisposição Genética para Doença; Variação Genética/genética; Software; Feminino; Marcadores Genéticos/genética; Heterozigoto; Sequenciamento de Nucleotídeos em Larga Escala/métodos; Humanos; Mutação INDEL/genética; Masculino; Linhagem; Polimorfismo de Nucleotídeo Único/genética

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Software / Predisposição Genética para Doença / Ligação Genética Idioma: En Ano de publicação: 2015 Tipo de documento: Article

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