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bp_mask_by_search(1p) [debian man page]

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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PSI-CD-HIT.PL(1)						   User Commands						  PSI-CD-HIT.PL(1)

NAME
psi-cd-hit.pl - runs similar algorithm like CD-HIT but using BLAST to calculate similarities DESCRIPTION
Usage psi-cd-hit [Options] Options -i in_dbname, required -o out_dbname, required -c clustering threshold (sequence identity), default 0.3 -ce clustering threshold (blast expect), default -1, it means by default it doesn't use expect threshold, but with positive value, the program cluster seqs if similarities meet either identity threshold or expect threshold -L coverage of shorter sequence ( aligned / full), default 0.0 -M coverage of longer sequence ( aligned / full), default 0.0 -R (1/0) use psi-blast profile? default 0 perform psi-blast / pdb-blast type search -G (1/0) use global identity? default 1 sequence identity calculated as total identical residues of local alignments / length of shorter seq if you prefer to use -G 0, it is suggested that you also use -L, such as -L 0.8, to prevent very short matches. -d length of description line in the .clstr file, default 30 if set to 0, it takes the fasta defline and stops at first space -l length_of_throw_away_sequences, default 10 -p profile search para, default "-a 2 -d nr80 -j 3 -F F -e 0.001 -b 500 -v 500" -bfdb profile database, default nr80 -s blast search para, default "-F F -e 0.000001 -b 100000 -v 100000" -be blast expect cutoff, default 0.000001 -b filename of list of hosts to run this program in parallel with ssh calls, you need provide a list of hosts -pbs No of jobs to send each time by PBS querying system you can not use both ssh and pbs at same time -k (1/0) keep blast raw output file, default 1 -rs steps of save restart file and clustering output, default 5000 everytime after process 5000 sequences, program write a restart file and current clustering information -restart restart file, readin a restart file if program crash, stoped, termitated, you can restart it by add a option "-restart sth.restart" -rf steps of re format blast database, default 200,000 if program clustered 200,000 seqs, it remove them from seq pool, and re format blast db to save time -local dir of local blast db, when run in parallel with ssh (not pbs), I can copy blast dbs to local drives on each node to save blast db reading time BUT, IT MAY NOT FASTER -J job, job_file, exe specific jobs like parse blast outonly DON'T use it, it is only used by this program itself -single files of ids those you known that they are singletons so I won't run them as queries ============================== by Weizhong Li, liwz@sdsc.edu ============================== If you find cd-hit useful, please kindly cite: "Clustering of highly homologous sequences to reduce thesize of large protein database", Weizhong Li, Lukasz Jaroszewski & Adam GodzikBioinformatics, (2001) 17:282-283 "Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences", Weizhong Li & Adam Godzik Bioinformatics, (2006) 22:1658-1659 psi-cd-hit.pl 4.6-2012-04-25 April 2012 PSI-CD-HIT.PL(1)
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