Your browser doesn't support javascript.
loading
CANOES: detecting rare copy number variants from whole exome sequencing data.
Backenroth, Daniel; Homsy, Jason; Murillo, Laura R; Glessner, Joe; Lin, Edwin; Brueckner, Martina; Lifton, Richard; Goldmuntz, Elizabeth; Chung, Wendy K; Shen, Yufeng.
Afiliação
  • Backenroth D; Departments of Systems Biology and Biomedical Informatics, Columbia University Medical Center, New York, NY 10032, USA JP Sulzberger Columbia Genome Center, Columbia University Medical Center, New York, NY 10032, USA.
  • Homsy J; Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA 02114, USA Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
  • Murillo LR; Departments of Pediatrics and Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Glessner J; Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Lin E; Departments of Systems Biology and Biomedical Informatics, Columbia University Medical Center, New York, NY 10032, USA Departments of Pediatrics and Medicine, Columbia University Medical Center, New York, NY 10032, USA.
  • Brueckner M; Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, USA.
  • Lifton R; Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, USA Howard Hughes Medical Institute, Yale University, New Haven, CT 06510, USA.
  • Goldmuntz E; Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Chung WK; Departments of Pediatrics and Medicine, Columbia University Medical Center, New York, NY 10032, USA ys2411@columbia.edu.
  • Shen Y; Departments of Systems Biology and Biomedical Informatics, Columbia University Medical Center, New York, NY 10032, USA JP Sulzberger Columbia Genome Center, Columbia University Medical Center, New York, NY 10032, USA ys2411@columbia.edu.
Nucleic Acids Res ; 42(12): e97, 2014 Jul.
Article em En | MEDLINE | ID: mdl-24771342
Assuntos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Algoritmos / Análise de Sequência de DNA / Variações do Número de Cópias de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Exoma Limite: Humans Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Algoritmos / Análise de Sequência de DNA / Variações do Número de Cópias de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Exoma Limite: Humans Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos