GeneSCF specifications


Unique identifier OMICS_10275
Name GeneSCF
Alternative name Gene Set Clustering based on Functional annotation
Software type Package/Module
Interface Command line interface
Restrictions to use Academic or non-commercial use
Input data The standard input for GeneSCF is plain text document (text/plain) containing a list of genes in the form of official gene symbols.
Output data The final output from GeneSCF is a table (text/tab-separated file, TSV) with list of ranked functions based on the number of hits from the user provided gene list. It also contains column with probability value (P-value) obtained by Fisher’s exact test using the contingency table and also columns containing false discovery rate (FDR) values using different multiple hypothesis correction methods.
Operating system Unix/Linux
Programming languages Perl, Shell (Bash)
License GNU General Public License version 3.0
Computer skills Advanced
Version 1.1
Stability Stable
Requirements R, ggplot
Maintained Yes


  • Animals
    • Homo sapiens



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  • person_outline Chandrasekhar Kanduri <>

GeneSCF articles


GeneSCF: a real-time based functional enrichment tool with support for multiple organisms.

2016 BMC Bioinformatics
PMID: 27618934
DOI: 10.1186/s12859-016-1250-z
GeneSCF institution(s)
Department of Medical Genetics, Institute of Biomedicine, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
GeneSCF funding source(s)
This work was supported by the grants from the Knut and Alice Wallenberg Foundation (KAW) (Dnr KAW 2014.0057), Swedish Foundation for Strategic Research (RB13-0204), Swedish Cancer Research foundation (Cancerfonden: Kontrakt no. 150796), the Swedish Research Council (VR-M: K2014-67X-20781-07-4), Barncancerfonden (PR2014/0147), Ingabritt Och Arne Lundbergs forskningsstiftelse and LUA/ALF.

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