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ADMIRE - Analysis of DNA methylation in genomic regions
=======================================================
ADMIRE is a semi-automatic analysis pipeline and visualization tool for Infinium HumanMethylation450K Chips.
Use ADMIRE online: https://bioinformatics.mpi-bn.mpg.de
Features
--------
- Automatic filtering and normalization
- Statistical testing and multiple testing correction
- Supports arbitrary number of samples and sample groups
- Differential methylation analysis on pre-calculated and individual genomic regions
- Provides ready-to-plug-in files for genome browsers (like IGV)
- Provides publication-ready figures for the most differentially methylated regions
- Performs gene set enrichment analysis on predefined and individual gene sets
Documentation
-------------
We have a extensive documentation with a use case available [here](http://admire.readthedocs.org).
Installation and Command-line usage
-----------------------------------
Make sure all prerequisites are met:
* [comb-p](https://github.com/brentp/combined-pvalues)
* [bedtools](https://github.com/arq5x/bedtools2)
* [R/Rscript](http://www.r-project.org/)
* [python - numpy](http://continuum.io/downloads)
* [python - matplotlib](http://continuum.io/downloads)
Install admire locally by running:
git clone https://github.molgen.mpg.de/loosolab/admire
export PATH=$PATH:dir/to/admire/src
```bash
Usage: admire [options]
Available options:
-c | Comma separated sample definition file (SampleSheet.csv)
-s | Tab separated sample definition file (design.txt)
-z | Compressed input of idat files (requires -c).
-e | Create quality control report in PDF
-r | Region file in bed format (regions.bed), use multiple -r parameters to calculate for multiple region files
-p | Detection p-value to exclude probes prior to analysis (0.01)
-t | Exclude probes where more than t% samples failed according to the detection p-value. (0.4)
-n | Normalization method (fn,swan,noob,illumina,raw,quantile)
-b | In case of functional normalization, skip noob background correction step
-d | In case of noob or functional normalization, skip dye correction step
-f | In case of quantile normalization, skip fixing outliers prior to analysis
-l | In case of quantile normalization, label samples as bad if their median signals are below a given value (10.5)
-m | In case of quantile normalization, remove bad samples
-q | Q-value cutoff for multiple testing correction (0.05)
-i | Render advanced plots for the best i regions (20)
-g | Gene set file for enrichment analysis, use multiple -g parameters to calculate enrichment over many gene sets
-o | tar-gz compress output into file given
-h | shows this help message
-v | shows version information
Options -c and -s are mutually exclusive.
```
How to cite?
------------
Please cite Preussner J, Bayer J, Kuenne C and Looso M. ADMIRE: ADMIRE: analysis and visualization of differential methylation in genomic regions using the Infinium HumanMethylation450 Assay. *Epigenetics & Chromatin* (**2015**), doi:10.1186/s13072-015-0045-1, when using admire in your work.
Contribute
----------
- Issue Tracker: github.molgen.mpg.de.com/loosolab/admire/issues
- Source Code: github.molgen.mpg.de.com/loosolab/admire
Support
-------
If you are having issues, please feel free to send an e-mail to Jens Preußner (jens.preussner@mpi-bn.mpg.de).
License
-------
The project is licensed under the MIT license.