accelerates sensitive genome searches
Now you can accelerate sensitive genome searches by an order of
magnitude using the SENCEL PARALIGN software. Running Sencel's
search software is the fastest
way to perform Smith-Waterman homology searches on standard hardware.
Furthermore, with the ParAlign algorithm, you can obtain
the same level of sensitivity at much higher speed. The speed is
achieved using Sencel's patent pending technology that relies on
the multimedia technology
embedded in most computers but not generally used by ordinary software.
You can evaluate the software by running free online
searches, or by registering
and downloading a copy of the
software and run it with a free evaluation license. See the PARALIGN
product sheet for an overview of its features.
PARALIGN version 5.0 released
PARALIGN version 5.0 was released on 9 April 2008. This release includes support for the
Linux i386 platform only. It works well with the latest releases of preformatted databases from NCBI. For more details about
the changes, see the release