PhenIX specifications

Unique identifier:
OMICS_09742
Interface:
Web user interface
Input data:
PhenIX requires a VCF file mapped to hg19/Gchr37, as well as a list of HPO terms representing the phenotype observed in the patient.
Stability:
Stable
Name:
Phenotypic Interpretation of eXomes
Restrictions to use:
None
Computer skills:
Basic
Maintained:
Yes
  • Animals
    • Homo sapiens

PhenIX support

Maintainer

  • Peter N. Robinson <>

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Publications

Institution(s)

Institute for Medical Genetics and Human Genetics, Charité Universitätsmedizin Berlin, Augustenburger Platz 1, Berlin, Germany; Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznan, Poland; Labor Berlin–Charité Vivantes GmbH, Humangenetik, Berlin, Germany; Max Planck Institute for Molecular Genetics, Ihnestr. Berlin, Germany; Berlin-Brandenburg Center for Regenerative Therapies, Charité Universitätsmedizin Berlin, Berlin, Germany; Max Delbrück Center for Molecular Medicine, Berlin, Germany; Cologne Center for Genomics, University of Cologne, Cologne, Germany; Agilent Technologies, Waldbronn, Germany; Department of Electrical Engineering, STADIUS Center for Dynamical Systems, Signal Processing and Data Analytics, KU Leuven, Leuven, Belgium; Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA; University Library and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Sciences University, Portland, OR, USA; Mouse Informatics Group, Wellcome Trust Sanger Institute, Hinxton, UK; Institute for Bioinformatics, Department of Mathematics and Computer Science, Freie Universität Berlin, Takustr. 9, Berlin, Germany

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