Hi Meabh, I'm not familiar with such tools, but maybe you can merge the original files with read-count back to your result file -> "Join two Datasets side by side on a specified field".
Cheers, Bjoern > I am new to Galaxy and am using it for analysis of BLAST results and > phylogeny. I have uploaded a file with contig names, the BLAST GI > number, and the total read count for each contig. When I use Galaxy to > 'Summarize taxonomy' and 'Draw phylogeny', I have lost the total read > counts. Eg. In the results of these it tells me how many contigs > belong to Fungi or Metazoa, whereas each contig actually has a > different number of reads. > Is there any way to reflect this in Galaxy? > I hope this makes sense! > ___________________________________________________________ > The Galaxy User list should be used for the discussion of > Galaxy analysis and other features on the public server > at usegalaxy.org. Please keep all replies on the list by > using "reply all" in your mail client. For discussion of > local Galaxy instances and the Galaxy source code, please > use the Galaxy Development list: > > http://lists.bx.psu.edu/listinfo/galaxy-dev > > To manage your subscriptions to this and other Galaxy lists, > please use the interface at: > > http://lists.bx.psu.edu/ > > To search Galaxy mailing lists use the unified search at: > > http://galaxyproject.org/search/mailinglists/ ___________________________________________________________ The Galaxy User list should be used for the discussion of Galaxy analysis and other features on the public server at usegalaxy.org. Please keep all replies on the list by using "reply all" in your mail client. For discussion of local Galaxy instances and the Galaxy source code, please use the Galaxy Development list: http://lists.bx.psu.edu/listinfo/galaxy-dev To manage your subscriptions to this and other Galaxy lists, please use the interface at: http://lists.bx.psu.edu/ To search Galaxy mailing lists use the unified search at: http://galaxyproject.org/search/mailinglists/
