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Paper Details

GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data.
Nat Genet
16
2023
CNV, CNVs, Copy number variants, GATK, exomes, exons, gCNV, human, per, rare coding CNVs
Author NameAffiliation
Mehrtash BabadiBroad Institute of MIT and Harvard
Laura GauthierBroad Institute of MIT and Harvard
Konrad J KarczewskiProgram in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Konrad J KarczewskiStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Konrad J KarczewskiMassachusetts General Hospital
Konrad J KarczewskiProgram in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Konrad J KarczewskiMassachusetts General Hospital
Konrad J KarczewskiStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Eric BanksBroad Institute of MIT and Harvard
Eric BanksBroad Institute of MIT and Harvard
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