Usage:

ame [options] <sequence file> <motif file>+

Description:

AME (Analysis of Motif Enrichment) scores a set of DNA sequences given a set of DNA-binding motifs, treating each position in the sequence as a the starting point of a possible binding event. AME counts the number of cases where the p-value of the binding event for each motif is below a given threshold, and performs a Fisher exact test versus the number of binding events in a background sequence set to determine the p-value of the count for each motif. The background set is appended to the main sequence set in the input file, and the offset within the file where the background starts is specified on the command line.

A previously described version of AME has a range of options not implemented in this version.

Input:

Output:

AME writes to a directory, ame_out, unless a different directory name is specified on the command line. The output directory contains outputs in two formats: HTML and plain text, in files named respectively ame.html and ame.txt.

Options:

The default output directory is ame_out, and is not overwritten (i.e., the default is the same as --o ame_out).

Notes

This version of AME does not implement a number of alternative scoring modes previously described. In the version, only Fisher exact test and total hits modes are implemented, with a fixed partition between foreground and background sequences. fix-partition in this version is therefore required rather than optional.

Citing ame

If AME is of use to you in your research, please cite:

Robert C. McLeay, Timothy L. Bailey (2009).
"Motif Enrichment Analysis: a unified framework and an evaluation on ChIP data."
BMC Bioinformatics 2010, 11:165, doi:10.1186/1471-2105-11-165.

Contact the authors

You can contact the authors via email:

Robert McLeay r.mcleay@imb.uq.edu.au, and Timothy Bailey t.bailey@imb.uq.edu.au.

Bug reports should be directed to Robert McLeay.