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Conbase: a software for unsupervised discovery of clonal somatic mutations in single cells through read phasing.
Hård, Joanna; Al Hakim, Ezeddin; Kindblom, Marie; Björklund, Åsa K; Sennblad, Bengt; Demirci, Ilke; Paterlini, Marta; Reu, Pedro; Borgström, Erik; Ståhl, Patrik L; Michaelsson, Jakob; Mold, Jeff E; Frisén, Jonas.
Afiliação
  • Hård J; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden. joanna.hard@ki.se.
  • Al Hakim E; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
  • Kindblom M; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
  • Björklund ÅK; Department of Cell and Molecular Biology, National Bioinformatics Infrastructure Sweden, Scilifelab, Uppsala University, Uppsala, Sweden.
  • Sennblad B; Department of Cell and Molecular Biology, National Bioinformatics Infrastructure Sweden, Scilifelab, Uppsala University, Uppsala, Sweden.
  • Demirci I; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
  • Paterlini M; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
  • Reu P; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
  • Borgström E; Division of Gene Technology, Scilifelab, KTH Royal Institute of Technology, Solna, Sweden.
  • Ståhl PL; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
  • Michaelsson J; Center for Infectious Medicine, Department of Medicine, Karolinska Institutet, Huddinge, Sweden.
  • Mold JE; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
  • Frisén J; Department of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden. jonas.frisen@ki.se.
Genome Biol ; 20(1): 68, 2019 04 01.
Article em En | MEDLINE | ID: mdl-30935387

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Análise de Célula Única / Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Análise de Célula Única / Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article