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MATLAB scripts that use miR target prediction databases (TargetScan 7.1, DIANA-microT CDS) to enrich a statistical analysis (Pearson's correlation, mutual information) of miR and mRNA data from the Ludwig Melbourne melanoma (LM-MEL) cell line panel data

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uomsystemsbiology/LMMEL-miR-miner

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LMMEL-miR-miner

A collection of scripts to predict putative miR-mRNA interactions where miR activity may be associated with melanoma phenotype switching. These scripts can be split by the programming language used:

MATLAB script(s)

The MATLAB script find_LMMEL_active_miRs.m (and associated functions wtihin MATLAB_functions), integrates miR target prediction databases (TargetScan 7.1, DIANA-microT CDS) to enrich a statistical analysis (Pearson's correlation, mutual information) of miR and mRNA data from the Ludwig Melbourne melanoma (LM-MEL) cell line panel data. The output from this script includes a number of putative miR:mRNA interactions.

R script(s)

The R scripts included here examine the TCGA SKCM raw data files and create text files which are used as input for the python scripts.

python script

The python script create_TCGA_plots.py is a standalone script which searches for specified miR:mRNA interactions within the TCGA SKCM data and plots figure panels which are matched to specific results identified from the cell line analaysis.

These scripts accompanies the manuscript:

MC Andrews/J Cursons, DG Hurley, M Anaka, JS Cebon, A Behren, EJ Crampin (2016). Systems analysis identifies miR-29b regulation of invasiveness in melanoma. BMC Molecular Cancer, (Accepted Nov 2016).

  • doi: to-be-assigned

Contacts

For further information, please contact:

Dr. Miles Andrews

  • Department of Genomic Medicine and Department of Surgical Oncology, MD Anderson Cancer Center, USA
  • ex: Cancer Immunobiology Laboratory, Olivia Newton-John Cancer Research Institute, Australia
  • mcandrews (at) mdanderson.org

Dr. Joe Cursons

  • Bioinformatics Division, Walter and Eliza Hall Institute of Medical Research, Australia
  • ex: Systems Biology Laboratory, University of Melbourne, Australia
  • cursons.j (at) wehi.edu.au

Dr. Daniel Hurley

  • Systems Biology Laboratory, University of Melbourne, Australia
  • daniel.hurley (at) unimelb.edu.au

Dr. Andreas Behren

  • Cancer Immunobiology Laboratory, Olivia Newton-John Cancer Research Institute, Australia
  • andreas.behren (at) onjcri.org.au

Prof. Jonathan Cebon

  • Cancer Immunobiology Laboratory, Olivia Newton-John Cancer Research Institute, Australia
  • jonathan.cebon (at) onjcri.org.au

Prof. Edmund Crampin

  • Systems Biology Laboratory, University of Melbourne, Australia
  • edmund.crampin (at) unimelb.edu.au

Virtual Reference Environment

For users unfamiliar with python, a Virtual Reference Environment will be available for this
project, containing all scripts, data and documentation in an easily-deployed format.

For further information on Virtual Reference Environments, please refer to the Online Documentation

Accompanying Data

These scripts use a number of data sources, including:

LM-MEL Cell Line Panel: miR and mRNA abundance data

TCGA Skin and Cutaneous Melanoma (SKCM) data: miR and mRNA abundance data from clinical samples

TargetScan v7.1

DIANA-microT CDS (v5.0)

miRTarBase

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MATLAB scripts that use miR target prediction databases (TargetScan 7.1, DIANA-microT CDS) to enrich a statistical analysis (Pearson's correlation, mutual information) of miR and mRNA data from the Ludwig Melbourne melanoma (LM-MEL) cell line panel data

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