Pair-wise and multiple alignment of genomic sequences with CHAOS and
DIALIGN
This service calculates pair-wise and multiple alignments of
genomic sequences using
CHAOS and
DIALIGN as
described in
If you use our software for your research, please
cite this article.
CHAOS is used to rapidly identify strong sequence similarities that
serve as anchor points to speed-up the DIALIGN alignment procedure.
Details about the CHAOS/DIALIGN procedure are available
here.
In addition, our web page now offers the interactive
multi-alignment visualisation
tool
ABC
by
Greg Cooper et al. (2004),
BMC Bioinformatics 2004, 5:192, see below.
Program Input: