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NAME

       sigma - Simple greedy multiple alignment of non-coding DNA sequences

SYNOPSIS

       sigma [options] [inputfile.fasta] [inputfile2.fasta ...]

       Each fasta file may contain a single sequence or multiple sequences;
       all sequences will be aligned together.

DESCRIPTION

       Sigma ("Simple greedy multiple alignment") is an alignment program with
       a new algorithm and scoring scheme designed specifically for non-coding
       DNA sequence. It uses a strategy of seeking the best possible gapless
       local alignments, at each step making the best possible alignment
       consistent with existing alignments, and scores the significance of the
       alignment based on the lengths of the aligned fragments and a
       background model which may be supplied or estimated from an auxiliary
       file of intergenic DNA. With real data, while "correctness" can’t be
       directly quantified for the alignment, running the PhyloGibbs motif
       finder on pre-aligned sequence suggests that Sigma’s alignments are
       superior.

OPTIONS

       -A --aligned_output
          Aligned, pretty-printed output (compare with -F option) (default:
          only this). See also -C.

       -b --bgprobfile filename
          Auxiliary file (in fasta format) from which to read background
          sequences (overridden by -B). Typically this is a file containing
          large quantities of similar non-coding sequence, from which
          background probabilities of single- and di-nucleotides may be
          estimated.

       -B --bgseqfile filename
          File containing background probabilities. The format is described
          further below.

       -C --caps_only
          Use only upper-case letters in output sequence, for compatibility
          with output of some other programs like ClustalW and MLagan. By
          default, output is mixed-case (as in Dialign), and lower-case bases
          are treated as not aligned.

       -F --fasta_output
          Multi-fasta output (can use both -A and -F in either order). See
          also -C.

       -n --ncorrel number
          Background correlation (default 2=dinucleotide; 1=single-site
          basecounts, 0=0.25 per base).

       -x, --significance number
          Set limit for how probable the match is by chance (default 0.002,
          smaller=more stringent).

       -h, --help
          Displays this list of options.

MORE HELP

       The "significance" parameter (-x) determines whether local alignments
       are accepted or rejected. The default at present is 0.002. Experiments
       on synthetic data (described in the paper) suggest that 0.002 is about
       the threshold where sigma fails to align phylogenetically-unrelated
       data that has moderate (yeast-like) dinucleotide correlation.

       Using a “background model” appropriate to the sequences being aligned
       greatly reduces spurious alignments on synthetic data (and, one hopes,
       on real data too). The simplest way to ensure this is to supply, via
       the -b parameter, a FASTA-format file containing large quantities of
       similar sequence data (eg, if one is aligning yeast sequences, supply a
       file containing all intergenic yeast sequence).

       Instead of this, if the single-site and dinucleotide frequencies are
       known already, they may be supplied in a file via the -B option. The
       file format should be: one entry per line, with the mononucleotide or
       dinucleotide (case-insensitive) followed by the frequency. (eg, "A
       0.3", "AT 0.16", etc on successive lines.) A sample file is in the
       "Background" subdirectory of the source distribution (on Debian
       systems, this file can be found in the
       /usr/share/doc/sigma-align/Background directory). A file like
       "yeast.nc.3.freq" in the "tests" subdirectory of the MEME source
       distribution works fine (trinucleotide counts are ignored).

REFERENCE

       Please cite Sigma: Rahul Siddharthan (2006) Multiple alignment of
       weakly-conserved non-coding DNA sequence BMC Bioinformatics 2006, 7:143
       doi:10.1186/1471-2105-7-143 Published 16 March 2006, available online
       at http://www.biomedcentral.com/1471-2105/7/143/

AUTHORS

       Rahul Siddharthan <rsidd@imsc.res.in>
          Wrote sigma. If you’re using Sigma for actual research, please let
          the author know so that he can alert you of bugfixes or new
          releases.

       Charles Plessy <charles-debian-nospam@plessy.org>
          Wrote the manpage in DocBook XML for the Debian distribution.

COPYRIGHT

       Copyright © 2006-2007 Rahul Siddharthan
       Copyright © 2006-2007 Charles Plessy

       Sigma is free software. You can redistribute it and/or modify it under
       the terms of the GNU General Public License as published by the Free
       Software Foundation.

       On Debian systems, the complete text of the GNU General Public License
       can be found in /usr/share/common-licenses/GPL.