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

Mehrtash Babadi^#¹, Jack M Fu^#^{2

3

4}, Samuel K Lee^#⁵, Andrey N Smirnov^#⁵, Laura D Gauthier⁵, Mark Walker^{5

3}, David I Benjamin⁵, Xuefang Zhao^{2

3

4}, Konrad J Karczewski^{2

6

7}, Isaac Wong^{2

3}, Ryan L Collins^{2

3}, Alba Sanchis-Juan^{2

3

4}, Harrison Brand^{2

3

4}, Eric Banks⁵, Michael E Talkowski^{8

9

10

11

12}

Affiliations

¹ Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA. mehrtash@broadinstitute.org.
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. talkowsk@broadinstitute.org.
⁹ Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA. talkowsk@broadinstitute.org.
¹⁰ Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. talkowsk@broadinstitute.org.
¹¹ Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA. talkowsk@broadinstitute.org.
¹² Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA. talkowsk@broadinstitute.org.

^# Contributed equally.

PMID: 38263447
DOI: 10.1038/s41588-024-01663-4

Published Erratum

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

Mehrtash Babadi et al. Nat Genet. 2024 Mar.

. 2024 Mar;56(3):553.

doi: 10.1038/s41588-024-01663-4.

Authors

Affiliations

¹ Data Sciences Platform, Broad Institute of MIT and Harvard, Cambridge, MA, USA. mehrtash@broadinstitute.org.
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. talkowsk@broadinstitute.org.
⁹ Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA. talkowsk@broadinstitute.org.
¹⁰ Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. talkowsk@broadinstitute.org.
¹¹ Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA. talkowsk@broadinstitute.org.
¹² Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA. talkowsk@broadinstitute.org.

^# Contributed equally.

PMID: 38263447
DOI: 10.1038/s41588-024-01663-4

No abstract available

PubMed Disclaimer

Erratum for

GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data.
Babadi M, Fu JM, Lee SK, Smirnov AN, Gauthier LD, Walker M, Benjamin DI, Zhao X, Karczewski KJ, Wong I, Collins RL, Sanchis-Juan A, Brand H, Banks E, Talkowski ME. Babadi M, et al. Nat Genet. 2023 Sep;55(9):1589-1597. doi: 10.1038/s41588-023-01449-0. Epub 2023 Aug 21. Nat Genet. 2023. PMID: 37604963 Free PMC article.

Publication types

Actions

LinkOut - more resources

Full Text Sources
- Nature Publishing Group

Save citation to file

Email citation

Add to Collections

Add to My Bibliography

Your saved search

Create a file for external citation management software

Your RSS Feed

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

Affiliations

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

Authors

Affiliations

Erratum for

Publication types

LinkOut - more resources

Full Text Sources