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

Backenroth, Daniel; Homsy, Jason; Murillo, Laura R; Glessner, Joe; Lin, Edwin; Brueckner, Martina; Lifton, Richard; Goldmuntz, Elizabeth; Chung, Wendy K; Shen, Yufeng.

Affiliation

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 de En | MEDLINE | ID: mdl-24771342

Sujet(s)

Texte intégral

Ajouter à My VHL

Imprimer

XML

PubMed Links

Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Algorithmes / Analyse de séquence d'ADN / Variations de nombre de copies de segment d'ADN / Séquençage nucléotidique à haut débit / Exome Limites: Humans Langue: En Journal: Nucleic Acids Res Année: 2014 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Royaume-Uni

Texte intégral

Ajouter à My VHL

Imprimer

XML

PubMed Links

Recherche sur Google