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Haplotype phasing and inheritance of copy number variants in nuclear families.
Palta, Priit; Kaplinski, Lauris; Nagirnaja, Liina; Veidenberg, Andres; Möls, Märt; Nelis, Mari; Esko, Tõnu; Metspalu, Andres; Laan, Maris; Remm, Maido.
Afiliación
  • Palta P; Department of Bioinformatics, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
  • Kaplinski L; Department of Bioinformatics, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia; Estonian Biocentre, Tartu, Estonia.
  • Nagirnaja L; Human Molecular Genetics Research Group, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
  • Veidenberg A; Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
  • Möls M; Estonian Biocentre, Tartu, Estonia; Chair of Mathematical Statistics, Institute of Mathematical Statistics, University of Tartu, Tartu, Estonia.
  • Nelis M; The Estonian Genome Center of University of Tartu, Tartu, Estonia.
  • Esko T; The Estonian Genome Center of University of Tartu, Tartu, Estonia; Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia; Division of Endocrinology, Boston Children's Hospital, Boston, Massachusetts, United States of America; Department of Genetics
  • Metspalu A; Estonian Biocentre, Tartu, Estonia; The Estonian Genome Center of University of Tartu, Tartu, Estonia; Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
  • Laan M; Human Molecular Genetics Research Group, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
  • Remm M; Department of Bioinformatics, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia; Estonian Biocentre, Tartu, Estonia.
PLoS One ; 10(4): e0122713, 2015.
Article en En | MEDLINE | ID: mdl-25853576
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Haplotipos / Genoma Humano / Variaciones en el Número de Copia de ADN Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Finlandia
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Haplotipos / Genoma Humano / Variaciones en el Número de Copia de ADN Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2015 Tipo del documento: Article País de afiliación: Finlandia