weight(1) [debian man page]
WEIGHT(1) General Commands Manual WEIGHT(1) NAME
weight - calculates sequence weights for an alignment SYNOPSIS
weight [-options] <alignment file> DESCRIPTION
This manual page documents briefly the weight command. weight is a program that calculates weights for a sequence alignment. OPTIONS
Available options: -b <f> Use BLOSUM weighting scheme at <f> fractional identity. -f <f> Filter out seqs w/ fractional ident > <x> [0-1]. -h Help; print version and usage info. -o <file> Save weight-annotated alignment in <outfile>. -p Use position based weight scheme (Henikoff & Henikoff). -s <n> Sample <n> sequences at random into a new alignment. -v Use Voronoi weight scheme (Sibbald & Argos). --informat <s> Specify alignment file format <s>. Allowed formats: SELEX, MSF, Clustal, a2m, PHYLIP. --quiet Suppress verbose banner. SEE ALSO
afetch(1), alistat(1), compalign(1), compstruct(1), revcomp(1), seqsplit(1), seqstat(1), sfetch(1), shuffle(1), sindex(1), sreformat(1), stranslate(1), AUTHOR
Sean Eddy HHMI/Department of Genetics Washington University School of Medicine 4444 Forest Park Blvd., Box 8510 St Louis, MO 63108 USA Phone: 1-314-362-7666 FAX : 1-314-362-2157 Email: eddy@genetics.wustl.edu This manual page was written by Nelson A. de Oliveira <naoliv@gmail.com>, for the Debian project (but may be used by others). Mon, 01 Aug 2005 15:28:08 -0300 WEIGHT(1)
Check Out this Related Man Page
seqstat(1) Biosquid Manual seqstat(1) NAME
seqstat - show statistics and format for a sequence file SYNOPSIS
seqstat [options] seqfile DESCRIPTION
seqstat reads a sequence file seqfile and shows a number of simple statistics about it. The printed statistics include the name of the format, the residue type of the first sequence (protein, RNA, or DNA), the number of sequences, the total number of residues, and the average and range of the sequence lengths. OPTIONS
-a Show additional verbose information: a table with one line per sequence showing name, length, and description line. These lines are prefixed with a * character to enable easily grep'ing them out and sorting them. -h Print brief help; includes version number and summary of all options, including expert options. -B (Babelfish). Autodetect and read a sequence file format other than the default (FASTA). Almost any common sequence file format is recognized (including Genbank, EMBL, SWISS-PROT, PIR, and GCG unaligned sequence formats, and Stockholm, GCG MSF, and Clustal align- ment formats). See the printed documentation for a complete list of supported formats. EXPERT OPTIONS
--informat <s> Specify that the sequence file is in format <s>, rather than the default FASTA format. Common examples include Genbank, EMBL, GCG, PIR, Stockholm, Clustal, MSF, or PHYLIP; see the printed documentation for a complete list of accepted format names. This option overrides the default expected format (FASTA) and the -B Babelfish autodetection option. --quiet Suppress the verbose header (program name, release number and date, the parameters and options in effect). SEE ALSO
afetch(1), alistat(1), compalign(1), compstruct(1), revcomp(1), seqsplit(1), sfetch(1), shuffle(1), sindex(1), sreformat(1), stranslate(1), weight(1). AUTHOR
Biosquid and its documentation are Copyright (C) 1992-2003 HHMI/Washington University School of Medicine Freely distributed under the GNU General Public License (GPL) See COPYING in the source code distribution for more details, or contact me. Sean Eddy HHMI/Department of Genetics Washington University School of Medicine 4444 Forest Park Blvd., Box 8510 St Louis, MO 63108 USA Phone: 1-314-362-7666 FAX : 1-314-362-2157 Email: eddy@genetics.wustl.edu Biosquid 1.9g January 2003 seqstat(1)