Provided by: dialign_2.2.1-7_amd64 
NAME
dialign2-2 - Multiple alignment program using the segment-to-segment approach
SYNOPSIS
dialign2-2 [options] [seq_file]
seq_file is the name of the input sequence file; this must be a multiple FASTA file (all sequences in one
file).
DESCRIPTION
dialign2-2 is a program that constructs alignments from gapfree pairs of similar segments of the
sequences. If (possibly) coding nucleic acid sequences are to be aligned, DIALIGN optionally translates
the compared `nucleic acid segments´ to `peptide segments´ according to the genetic code -- without
presupposing any of the three possible reading frames, so all combinations of reading frames get checked
for significant similarity.
By default, DIALIGN creates a single file containing
• An alignment of the input sequences in DIALIGN format.
• The same alignment in FASTA format.
• A sequence tree in PHYLIP format. This tree is constructed by applying the UPGMA clustering method to
the DIALIGN similarity scores. It roughly reflects the different degrees of similarity among
sequences. For detailed phylogenetic analysis, we recommend the usual methods for phylogenetic
reconstruction.
The format of the output files is documented in /usr/share/doc/dialign/USER_GUIDE.gz. The FASTA, CLUSTALW
and MSF output formats are optionally available (see OPTIONS).
OPTIONS
-afc
Creates additional output file "*.afc" containing data of all fragments considered for alignment.
WARNING: this file can be HUGE!
-afc_v
Like "-afc" but verbose: fragments are explicitly printed. WARNING: this file can be EVEN BIGGER!
-anc
Anchored alignment. Requires a file seq_file.anc containing anchor points.
-cs
If segments are translated, not only the `Watson strand´ but also the `Crick strand´ is looked at.
-cw
Additional output file in CLUSTAL W format.
-ds
`DNA alignment speed up´. Non-translated nucleic acid fragments are taken into account only if they
start with at least two matches. Speeds up DNA alignment at the expense of sensitivity.
-fa
Additional output file in FASTA format.
-ff
Creates file *.frg containing information about all fragments that are part of the respective optimal
pairwise alignmnets plus information about consistency in the multiple alignment.
-fn out_file
Output files are named out_file.extension.
-fop
Creates file *.fop containing coordinates of all fragments that are part of the respective pairwise
alignments.
-fsm
Creates file *.fsm containing coordinates of all fragments that are part of the final alignment
-iw
Overlap weights switched off (by default, overlap weights are used if up to 35 sequences are
aligned). This option speeds up the alignment but may lead to reduced alignment quality.
-lgs
`Long genomic sequences´ - combines the following options: -ma, -thr 2, -lmax 30, -smin 8, -nta, -ff,
-fop, -ff, -cs, -ds, -pst.
-lgs_t
Like "-lgs" but with all segment pairs assessed at the peptide level (rather than ´mixed alignments´
as with the "-lgs" option). Therefore faster than -lgs but not very sensitive for non-coding regions.
-lmax x
Maximum fragment length = x (default: x = 40 or x = 120 for `translated´ fragments). Shorter x speeds
up the program but may affect alignment quality.
-lo
(Long Output) Additional file *.log with information abut fragments selected for pairwise alignment
and about consistency in multi-alignment proceedure.
-ma
`mixed alignments´ consisting of P-fragments and N-fragments if nucleic acid sequences are aligned.
-mask
Residues not belonging to selected fragments are replaced by `*´ characters in output alignment
(rather than being printed in lower-case characters)
-mat
Creates file *mat with substitution counts derived from the fragments that have been selected for
alignment.
-mat_thr t
Like "-mat" but only fragments with weight score > t are considered.
-max_link
"Maximum linkage" clustering used to construct sequence tree (instead of UPGMA).
-min_link
"Minimum linkage" clustering used.
-mot
"Motif" option.
-msf
Separate output file in MSF format.
-n
Input sequences are nucleic acid sequences. No translation of fragments.
-nt
Input sequences are nucleic acid sequences and `nucleic acid segments´ are translated to `peptide
segments´.
-nta
`No textual alignment´. Textual alignment suppressed. This option makes sense if other output files
are of intrest -- e.g. the fragment files created with -ff, -fop, -fsm or -lo.
-o
Fast version, resulting alignments may be slightly different.
-ow
Overlap weights enforced (By default, overlap weights are used only if up to 35 sequences are aligned
since calculating overlap weights is time consuming). Warning: overlap weights generally improve
alignment quality but the running time increases in the order O(n^4) with the number of sequences.
This is why, by default, overlap weights are used only for sequence sets with < 36 sequences.
-pst
"Print status". Creates and updates a file *.sta with information about the current status of the
program run. This option is recommended if large data sets are aligned since it allows the user to
estimate the remaining running time.
-smin x
Minimum similarity value for first residue pair (or codon pair) in fragments. Speeds up protein
alignment or alignment of translated DNA fragments at the expense of sensitivity.
-stars x
Maximum number of `*´ characters indicating degree of local similarity among sequences. By default,
no stars are used but numbers between 0 and 9, instead.
-stdo
Results written to standard output.
-ta
Standard textual alignment printed (overrides suppression of textual alignments in special options,
e.g. -lgs).
-thr x
Threshold T = x.
-xfr
"Exclude fragments". List of fragments can be specified that are NOT considered for pairwise
alignment.
General remark: If contradictory options are used, subsequent options override previous ones, e.g.:
dialign2-2 -nt -n seq_file runs the program with the "-n" option (no translation!), while dialign2-2 -n
-nt seq_file runs it with the "-nt" option (translation!).
SEE ALSO
The full documentation is in /usr/share/doc/dialign/.
The website of dialign: http://dialign.gobics.de/
DIALIGN2 has been re-implemented in dialign-tx(1). See http://dialign-tx.gobics.de/
ENVIRONMENT VARIABLES
You can create an environment variable `DIALIGN2_DIR´ pointing to a directory where the substitution
matrices are (see FILES). When installed from the Debian package, it is not necessary to set this
environnement variable to run DIALIGN.
FILES
DIALIGN2 needs the files tp400_dna, tp400_prot, tp400_trans and BLOSUM. When DIALIGN is installed from
the Debian package, they are stored in /usr/share/dialign/.
DIALIGN 2 uses the BLOSUM62 amino acid substitution matrix. In the current version, it is NOT possible to
replace BLOSUM62 by other similarity matrices.
REFERENCE
B. Morgenstern (1999). DIALIGN 2: improvement of the segment-to-segment approach to multiple sequence
alignment. Bioinformatics 15, 211 - 218. Public research assisted by DIALIGN should cite this article.
AUTHORS
Burkhard Morgenstern <bmorgen@gwdg.de> Author of DIALIGN Said Abdeddaim Author of DIALIGN Charles Plessy <plessy@debian.org> Wrote this manpage
COPYRIGHT
DIALIGN was written by Burkhard Morgenstern and Said Abdeddaim at University of Bielefeld (FSPM and
International Graduate School in Bioinformatics and Genome Research), GSF (ISG, IBB, MIPS/IBI), North
Carolina State University, Universite de Rouen, MPI fuer Biochemie (Martinsried), University of
Goettingen, Institute of Microbiology and Genetics.
This manual page was adapted from the DIALIGN manual by Charles Plessy <plessy@debian.org> for the Debian
system (but may be used by others). Permission is granted to copy, distribute and/or modify this document
under the terms of the GNU Lesser General Public License, Version 2.1 any later version published by the
Free Software Foundation.
On Debian systems, the complete text of the GNU Lesser General Public License can be found in
/usr/share/common-licenses/LGPL.
Copyright © 1999 Burkhard Morgenstern (for DIALIGN)
Copyright © 2006, 2007, 2008 Charles Plessy (for this manpage)