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Linked-read analysis identifies mutations in single-cell DNA-sequencing data.
Bohrson, Craig L; Barton, Alison R; Lodato, Michael A; Rodin, Rachel E; Luquette, Lovelace J; Viswanadham, Vinay V; Gulhan, Doga C; Cortés-Ciriano, Isidro; Sherman, Maxwell A; Kwon, Minseok; Coulter, Michael E; Galor, Alon; Walsh, Christopher A; Park, Peter J.
Afiliación
  • Bohrson CL; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
  • Barton AR; Bioinformatics and Integrative Genomics PhD Program, Harvard Medical School, Boston, MA, USA.
  • Lodato MA; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
  • Rodin RE; Bioinformatics and Integrative Genomics PhD Program, Harvard Medical School, Boston, MA, USA.
  • Luquette LJ; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.
  • Viswanadham VV; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, MA, USA.
  • Gulhan DC; Broad Institute, Cambridge, MA, USA.
  • Cortés-Ciriano I; Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA.
  • Sherman MA; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, MA, USA.
  • Kwon M; Broad Institute, Cambridge, MA, USA.
  • Coulter ME; Program in Neuroscience and Harvard/MIT MD-PHD Program, Harvard Medical School, Boston, MA, USA.
  • Galor A; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
  • Walsh CA; Bioinformatics and Integrative Genomics PhD Program, Harvard Medical School, Boston, MA, USA.
  • Park PJ; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Nat Genet ; 51(4): 749-754, 2019 04.
Article en En | MEDLINE | ID: mdl-30886424
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mutación Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mutación Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos