Mercurial > repos > pjbriggs > macs21
diff macs21_wrapper.xml @ 8:78c15c0a96ae draft
Uploaded new version with minor fixes and updates to help text.
author | pjbriggs |
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date | Tue, 21 Apr 2015 10:33:52 -0400 |
parents | 344dd37d1704 |
children | 7aecd0908b3c |
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--- a/macs21_wrapper.xml Tue Apr 21 08:29:16 2015 -0400 +++ b/macs21_wrapper.xml Tue Apr 21 10:33:52 2015 -0400 @@ -328,50 +328,56 @@ <!--none yet for macs2--> </tests> <help> - -.. class:: warningmark - -**This is a modified version of the standard Galaxy toolshed "MACS2" tool, -which has been customised for users at the University of Manchester to work -with MACS 2.1.0.** - -It is based on the 16:14f378e35191 revision of the tool at - - * http://toolshed.g2.bx.psu.edu/view/modencode-dcc/macs2 - ------- - **What it does** -With the improvement of sequencing techniques, chromatin immunoprecipitation -followed by high throughput sequencing (ChIP-Seq) is getting popular to study -genome-wide protein-DNA interactions. To address the lack of powerful ChIP-Seq -analysis method, we present a novel algorithm, named Model-based Analysis of -ChIP-Seq (MACS), for identifying transcript factor binding sites. MACS captures -the influence of genome complexity to evaluate the significance of enriched -ChIP regions, and MACS improves the spatial resolution of binding sites through -combining the information of both sequencing tag position and orientation. MACS -can be easily used for ChIP-Seq data alone, or with control sample with the -increase of specificity. +MACS (Model-based Analysis of ChIP-seq) provides algorithms for transcript +factor binding sites. The program can be used either for ChIP-Seq data alone, +or with control sample datat to improve specificity. -View the original MACS2 documentation: +View the MACS2 documentation at: https://github.com/taoliu/MACS/blob/master/README.rst ------ **Usage** -**Peak Calling**: Main MACS2 Function to Call peaks from alignment results. +The tool interfaces with two main functions in MACS: -**Compare .bdg files**: Deduct noise by comparing two signal tracks in bedGraph. - + * **callpeaks** (the main function) calls peaks from alignment results + * **bdgcmp** deducts noise by comparing two signal tracks in bedGraph format. ------ -**Citation** +**Credits** + +This Galaxy tool was based on the MACS2 tool hosted in the Galaxy toolshed at + + * http://toolshed.g2.bx.psu.edu/view/modencode-dcc/macs2 -For the underlying tool, please cite Zhang Y, Liu T, Meyer CA, Eeckhoute J, Johnson DS, Bernstein BE, Nusbaum C, Myers RM, Brown M, Li W, Liu XS. Model-based analysis of ChIP-Seq (MACS). Genome Biol. 2008;9(9):R137. +(specifically the 16:14f378e35191 revision of the tool) which is credited to Ziru +Zhou. This version is a reimplemented version developed within the Bioinformatics +Core Facility at the University of Manchester, which uses more up-to-date Galaxy +syntax and adds some extra features. + +The tool runs Tao Liu's MACS2 software: + + * https://github.com/taoliu/MACS + +The reference for MACS is: -Integration of MACS2 with Galaxy performed by Ziru Zhou ( ziruzhou@gmail.com ). Please send your comments/questions to modENCODE DCC at help@modencode.org. + * Zhang Y, Liu T, Meyer CA, Eeckhoute J, Johnson DS, Bernstein BE, Nusbaum C, + Myers RM, Brown M, Li W, Liu XS. Model-based analysis of ChIP-Seq (MACS). + Genome Biol. 2008;9(9):R137. + +Please kindly acknowledge both this Galaxy tool and the MACS2 package if you +use it. </help> + <citations> + <!-- + See https://wiki.galaxyproject.org/Admin/Tools/ToolConfigSyntax#A.3Ccitations.3E_tag_set + Can be either DOI or Bibtex + Use http://www.bioinformatics.org/texmed/ to convert PubMed to Bibtex + --> + <citation type="doi">10.1186/gb-2008-9-9-r137</citation> + </citations> </tool>