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AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data.
Quinodoz, Mathieu; Peter, Virginie G; Bedoni, Nicola; Royer Bertrand, Béryl; Cisarova, Katarina; Salmaninejad, Arash; Sepahi, Neda; Rodrigues, Raquel; Piran, Mehran; Mojarrad, Majid; Pasdar, Alireza; Ghanbari Asad, Ali; Sousa, Ana Berta; Coutinho Santos, Luisa; Superti-Furga, Andrea; Rivolta, Carlo.
Afiliação
  • Quinodoz M; Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland.
  • Peter VG; Department of Ophthalmology, University of Basel, Basel, Switzerland.
  • Bedoni N; Department of Genetics and Genome Biology, University of Leicester, Leicester, UK.
  • Royer Bertrand B; Institute of Molecular and Clinical Ophthalmology Basel (IOB), Basel, Switzerland.
  • Cisarova K; Department of Ophthalmology, University of Basel, Basel, Switzerland.
  • Salmaninejad A; Department of Genetics and Genome Biology, University of Leicester, Leicester, UK.
  • Sepahi N; Institute of Experimental Pathology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
  • Rodrigues R; Service of Medical Genetics, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
  • Piran M; Service of Medical Genetics, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
  • Mojarrad M; Service of Medical Genetics, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
  • Pasdar A; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Ghanbari Asad A; Noncommunicable Diseases Research Center, Fasa University of Sciences, Fasa, Iran.
  • Sousa AB; Department of Medical Genetics, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte (CHULN), Lisbon Academic Medical Center (CAML), Lisbon, Portugal.
  • Coutinho Santos L; Noncommunicable Diseases Research Center, Fasa University of Sciences, Fasa, Iran.
  • Superti-Furga A; Bioinformatics and Computational Biology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Rivolta C; Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Nat Commun ; 12(1): 518, 2021 01 22.
Article em En | MEDLINE | ID: mdl-33483490
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Software / Genoma Humano / Mapeamento Cromossômico / Biologia Computacional / Polimorfismo de Nucleotídeo Único / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Suíça
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Software / Genoma Humano / Mapeamento Cromossômico / Biologia Computacional / Polimorfismo de Nucleotídeo Único / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Suíça