- Unique identifier:
- Software type:
- Restrictions to use:
- Operating system:
- BSD 2-clause “Simplified” License, GNU General Public License version 3.0
- NumPy, SciPy, pandas, PyTables, Statsmodels, Matplotlib
- Alternative name:
- Command line interface, Graphical user interface
- Input format:
- Programming languages:
- Computer skills:
- Douglas M. Fowler <>
- Alan Rubin <>
Previous version: http://depts.washington.edu/sfields/software/enrich/ http://depts.washington.edu/sfields/software/enrich/docs/0.2/enrich.html
No open topic.
(Fowler et al., 2011)
Enrich: software for analysis of protein function by enrichment and depletion of variants.
PMID: 22006916 DOI: 10.1093/bioinformatics/btr577
(Rubin et al., 2017)
A statistical framework for analyzing deep mutational scanning data.
Bioinformatics Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia; Department of Medical Biology, University of Melbourne, Melbourne, VIC, Australia; Bioinformatics and Cancer Genomics Laboratory, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia; Department of Genome Sciences, University of Washington, Seattle, WA, USA; Institute for Protein Design, University of Washington, Seattle, WA, USA; Department of Pathology, University of Washington, Seattle, WA, USA; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, VIC, Australia; Department of Mathematics and Statistics, University of Melbourne, Melbourne, VIC, Australia; Department of Bioengineering, University of Washington, Seattle, WA, USA
Supported by the National Institute of General Medical Sciences (1R01GM109110 and 5R24GM115277 and P41GM103533); the National Institute of Biomedical Imaging and Bioengineering (5R21EB020277); the Washington Research Foundation (Washington Research Foundation Innovation Postdoctoral Fellowship) and the National Health and Medical Research Council of Australia (Program Grant 1054618).
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