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Paper Details

Combining callers improves the detection of copy number variants from whole-genome sequencing.
Eur J Hum Genet
18
2022
Author NameAffiliation
Manuel HoltgreweBerlin Institute of Health
Manuel HoltgreweCharite Universitatsmedizin Berlin
Marten J??gerCharite Universitatsmedizin Berlin
Marten J??gerBerlin Institute of Health
Malte SpielmannInstitute of Medical and Human Genetics, Charite Universitatsmedizin
Malte SpielmannMax Planck Institute for Molecular Genetics
Malte SpielmannInstitute of Human Genetics, University of Lubeck
Peter M KrawitzInstitut fur Genomische Statistik und Bioinformatik
Denise HornInstitute of Medical and Human Genetics, Charite Universitatsmedizin
Stefan MundlosInstitute of Medical and Human Genetics, Charite Universitatsmedizin
Stefan MundlosMax Planck Institute for Molecular Genetics
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