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bp_search2alnblocks(1p) [debian man page]

BP_SEARCH2ALNBLOCKS(1p) 				User Contributed Perl Documentation				   BP_SEARCH2ALNBLOCKS(1p)

NAME
search2alnblocks - Turn SearchIO parseable reports(s) into a set of aligned blocks SYNOPSIS
search2alnblocks --minid PERCENTID --minlen LEN --minevalue EVALUE file1. blast file2.blast ...> out.fas DESCRIPTION
This script will parse and filter BLAST (or other formats Bio::SearchIO can parse) output and format the alignment as blocks of alignments based on the HSPs. Note this can only work if the input file parsed contains the necessary. Typically this can be used to turn BLAST output into a FASTA alignment format for input into the QRNA comparative gene finder for RNA genes (E.Rivas). OPTIONS
--maxevalue Maximum E-value for an HSP --minevalue Minimum E-value for an HSP --minlen Minimum length of an HSP [default 0] --maxid Maximum Percent Id [default 100] (to help remove sequences which are really close) --minid Minimum Percent Identity for an HSP [default 0] -i/--input An optional input filename (expects input on STDIN by default) -o/--output An optional output filename (exports to STDOUT by default) -f/--format Specify a different Search Alignment format- {fasta, axt, waba, blast, blastxml} are all permitted although the format must have actual alignment sequence for this script to work See L<Bio::SearchIO> for more information. -of/--outformat Output format for the alignment blocks, anything L<Bio::AlignIO> supports. -v/--verbose Turn on debugging AUTHOR - Jason Stajich Jason Stajich, jason-at-bioperl-dot-org. perl v5.14.2 2012-03-02 BP_SEARCH2ALNBLOCKS(1p)

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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)
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