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Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data.
Babadi, Mehrtash; Fu, Jack M; Lee, Samuel K; Smirnov, Andrey N; Gauthier, Laura D; Walker, Mark; Benjamin, David I; Zhao, Xuefang; Karczewski, Konrad J; Wong, Isaac; Collins, Ryan L; Sanchis-Juan, Alba; Brand, Harrison; Banks, Eric; Talkowski, Michael E.
Afiliación
  • Babadi M; Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA. mehrtash@broadinstitute.org.
  • Fu JM; Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Lee SK; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Smirnov AN; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
  • Gauthier LD; Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Walker M; Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Benjamin DI; Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Zhao X; Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Karczewski KJ; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Wong I; Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Collins RL; Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Sanchis-Juan A; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Brand H; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
  • Banks E; Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Talkowski ME; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
Nat Genet ; 56(3): 553, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38263447

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos