Pair-wise and multiple alignment of genomic sequences with CHAOS and
This service calculates pair-wise and multiple alignments of
genomic sequences using CHAOS
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
Greg Cooper et al. (2004),
BMC Bioinformatics 2004, 5:192
, see below.