Ancestral Reconstruction Pipeline: Difference between revisions

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* -g gid1,gid2,gid3,gid4... <list of common separated coge genome ids>  
* -g gid1,gid2,gid3,gid4... <list of common separated coge genome ids>  
* -w w1,w2,w3,w4 <list of comma separated weights for genomes -- note these are paired ordered data with the -g option?>  
* -w w1,w2,w3,w4 <list of comma separated weights for genomes -- note these are paired ordered data with the -g option?>  
-
*-wa <threshold minimum adjacency score for keeping a contig.  Called 'weightOfAdjacent' in original config file>
*-cl <threshold minimum contig length.  Called 'minimumGeneGroupLength' in original config file>
*-b <Number of bins for assignment to ancestral chromosomes.  Called 'AncChrNumber' in original config file> (Note:  this may be removed if this info can be derived from the input.>
Note:  genomeInContigIndex is specified in the config file.  This is the weighting for each subgenome.  Need to discuss how best to deal with these.

Revision as of 21:34, 25 April 2014

Plan for refactoring

GetGenomes: remove config file, add option to specify output dir for output files

  • -d<directory of input synmap files>
  • -g gid1,gid2,gid3,gid4... <list of common separated coge genome ids>
  • -w w1,w2,w3,w4 <list of comma separated syntenic depths for genomes -- note these are paired ordered data with the -g option?>
  • -s < subgenome_file>
  • -o <output directory for SubGenomeInGeneOrder OrthologSets GenomeInString files>

MWMPython: http://jorisvr.nl/maximummatching.html needs command line options for

  • -i <input file or directory>
      • File type is a set of vertex vertex weight
      • note: if directory, will batch process all files
  • -o <outfile or directory>

GetContigInput

  • Remove config file dependency
  • -g gid1,gid2,gid3,gid4... <list of common separated coge genome ids>
  • -w w1,w2,w3,w4 <list of comma separated weights for genomes -- note these are paired ordered data with the -g option?>
  • -wa <threshold minimum adjacency score for keeping a contig. Called 'weightOfAdjacent' in original config file>
  • -cl <threshold minimum contig length. Called 'minimumGeneGroupLength' in original config file>
  • -b <Number of bins for assignment to ancestral chromosomes. Called 'AncChrNumber' in original config file> (Note: this may be removed if this info can be derived from the input.>

Note: genomeInContigIndex is specified in the config file. This is the weighting for each subgenome. Need to discuss how best to deal with these.