Author Correction: GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data

Affiliations

• ¹ Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA. [email protected].
• ² Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
• ³ Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
• ⁴ Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
• ⁵ Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
• ⁶ Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
• ⁷ Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
• ⁸ Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA. [email protected].
• ⁹ Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA. [email protected].
• ¹⁰ Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. [email protected].
• ¹¹ Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA. [email protected].
• ¹² Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA. [email protected].