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ClinCNV: multi-sample germline CNV detection in NGS data

View ORCID ProfileGerman Demidov, View ORCID ProfileMarc Sturm, View ORCID ProfileStephan Ossowski
doi: https://doi.org/10.1101/2022.06.10.495642
German Demidov
1Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany
2Center for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain
3Universitat Pompeu Fabra (UPF), Barcelona, Spain
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  • For correspondence: german.m.demidov@gmail.com
Marc Sturm
1Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany
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Stephan Ossowski
1Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany
2Center for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain
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Article Information

doi 
https://doi.org/10.1101/2022.06.10.495642
History 
  • June 13, 2022.
Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.

Author Information

  1. German Demidov1,2,3,*,
  2. Marc Sturm1 and
  3. Stephan Ossowski1,2
  1. 1Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany
  2. 2Center for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain
  3. 3Universitat Pompeu Fabra (UPF), Barcelona, Spain
  1. ↵*Corresponding author; email: german.m.demidov{at}gmail.com
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Posted June 13, 2022.
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ClinCNV: multi-sample germline CNV detection in NGS data
German Demidov, Marc Sturm, Stephan Ossowski
bioRxiv 2022.06.10.495642; doi: https://doi.org/10.1101/2022.06.10.495642
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ClinCNV: multi-sample germline CNV detection in NGS data
German Demidov, Marc Sturm, Stephan Ossowski
bioRxiv 2022.06.10.495642; doi: https://doi.org/10.1101/2022.06.10.495642

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