bp_search2tribe(1p) [debian man page]

BP_SEARCH2TRIBE(1p)					User Contributed Perl Documentation				       BP_SEARCH2TRIBE(1p)

NAME

       search2tribe - Turn SearchIO parseable reports(s) into TRIBE matrix

SYNOPSIS

       Usage:
	 search2tribe [-o outputfile] [-f reportformat] [-w/--weight] file1 file2 ..

DESCRIPTION

       This script is probably too slow for most people's uses.  It is better to use something like scripts/searchio/fastam9_to_table, -m 9 output
       from BLAST, or the blast2table from the BLAST O'Reilly book to get a tabular output from these programs and then feed the table into MCL
       with the mcxdeblast script and the --m9 option.

       This script will turn a protein Search report (BLASTP, FASTP, SSEARCH) into a Markov Matrix for TribeMCL clustering.

       The options are:

	  -o filename	       - the output filename [default STDOUT]
	  -f format	       - search result format (blast, fasta)
				 (ssearch is fasta format). default is blast.
	  -w or --weight VALUE - Change the default weight for E(0.0) hits
				 to VALUE (default=200 (i.e. 1e-200) )
	  -h		       - this help menu

       Additionally specify the filenames you want to process on the command-line.  If no files are specified then STDIN input is assumed.  You
       specify this by doing: search2tribe < file1 file2 file3

AUTHOR

       Jason Stajich, jason-at-bioperl-dot-org

perl v5.14.2							    2012-03-02						       BP_SEARCH2TRIBE(1p)

BP_MASK_BY_SEARCH(1p)					User Contributed Perl Documentation				     BP_MASK_BY_SEARCH(1p)

NAME

       mask_by_search - mask sequence(s) based on its alignment results

SYNOPSIS

	 mask_by_search.pl -f blast genomefile blastfile.bls > maskedgenome.fa

DESCRIPTION

       Mask sequence based on significant alignments of another sequence.  You need to provide the report file and the entire sequence data which
       you want to mask.  By default this will assume you have done a TBLASTN (or TFASTY) and try and mask the hit sequence assuming you've
       provided the sequence file for the hit database.  If you would like to do the reverse and mask the query sequence specify the -t/--type
       query flag.

       This is going to read in the whole sequence file into memory so for large genomes this may fall over.  I'm using DB_File to prevent keeping
       everything in memory, one solution is to split the genome into pieces (BEFORE you run the DB search though, you want to use the exact file
       you BLASTed with as input to this program).

       Below the double dash (--) options are of the form --format=fasta or --format fasta or you can just say -f fasta

       By -f/--format I mean either are acceptable options.  The =s or =n or =c specify these arguments expect a 'string'

       Options:
	   -f/--format=s    Search report format (fasta,blast,axt,hmmer,etc)
	   -sf/--sformat=s  Sequence format (fasta,genbank,embl,swissprot)
	   --hardmask	    (booelean) Hard mask the sequence
			    with the maskchar [default is lowercase mask]
	   --maskchar=c     Character to mask with [default is N], change
			    to 'X' for protein sequences
	   -e/--evalue=n    Evalue cutoff for HSPs and Hits, only
			    mask sequence if alignment has specified evalue
			    or better
	   -o/--out/
	   --outfile=file   Output file to save the masked sequence to.
	   -t/--type=s	    Alignment seq type you want to mask, the
			    'hit' or the 'query' sequence. [default is 'hit']
	   --minlen=n	    Minimum length of an HSP for it to be used
			    in masking [default 0]
	   -h/--help	    See this help information

AUTHOR - Jason Stajich
       Jason Stajich, jason-at-bioperl-dot-org.

perl v5.14.2							    2012-03-02						     BP_MASK_BY_SEARCH(1p)