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Python Package for RNA structure prediction analysis.

Project description


This package is used for maniputating genome annotation and seqeunce files, such as Bed, GenePred, BAM, Wiggle and BigWig formats. Users interested in this package should contact for details. This package uses the Vienna RNA Package lib and H directories (external/RNAlib/fold) and RNAStructure libs (external/RNAlib/plot), and users should read the COPYING or ReadMe.txt files inside and behave accordingly. All files are copyrighted, but license is hereby granted for personal, academic and non-profit use. Commercial users should contact



PREREQUISITES 1. python 2.7, python-dev 2. numpy >= 1.4.1 (automatically installed) 3. ngslib >= 1.1.10 for NGS data processing (automatically installed) 4. fisher >= 0.1.4 for fisher exact test ((automatically installed) 4. sfold 2.2 stand-alone executable (


  1. Install from Python Package Index ( > easy_install –prefix=$HOME/local multifold
  2. Install from source file (including the demo example files) >easy_install –editable –build-directory package_source/ multifold >cd package_source >python install –prefix=install_path
  3. sfold 2.2
    Download the stand-alone executable from
    Run configure file
    >cd SFOLD2.2_HOME >./configure
    Test sfold in command line before use:
    If successful, add sfold binary file to system PATH by:


  • Data formats:
    FastD, FastC, FastS and EFastS to represent data used in MultiFold.
  • IO:
    Readers for each data format
  • Predictor:
    Wrappers of a series of RNA secondary structure prediction tools. RNAfold, mfold, UNAFold, sfold, et. al. Note: make sure the command/program is callable in shell before call it in MultiFold.
  • Algorithm:
    EM algoritm, Boltzmann sampling, structure distance calculation, et. al.
  • Utils:
    Utilites. Temperature conversion, structure format conversion, et. al.
  • ThreadSafeFile:
    Used in multiple processing procedures.

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