Sorry I should have copied the users group on this:

Yes that is a problem we have encountered. We have basically decided to use each part 
for what it is "advertised" to do best:  we use the HMM result as being slightly more 
accurate for eukaryotic data "For eukaryotic data, SignalP-HMM has a substantially 
improved discrimination between signal peptides and uncleaved signal anchors" (quote 
taken from their site) but take the cleavage position from the neural networks part 
"but it has a slightly lower accuracy in predicting the precise location of the 
cleavage site". The HMM result also has the advantage as well of being less ambigious 
ie it makes a clear call rather than leaving it to you to decide how many yes's 
constitutes a positive result. Hope this helps...

Sarah

Sarah Larkin McQuaid, PhD.
Sr. Scientific Investigator/Bioinformatics Group Leader,
Dept. of Cell and Molecular Biology,
Amylin Pharmaceuticals, Inc.
Phone: 858.642.7357
http://www.amylin.com

-----Original Message-----
From: Kerrie Dunstan [mailto:[EMAIL PROTECTED]]
Sent: Wednesday, December 11, 2002 3:26 PM
To: [EMAIL PROTECTED]
Subject: [artemis-users] signalP anyone??


You guys are my last resort! Sorry this is not
directly artemis-related.

Has anyone been using SignalP? If so do you use the
HMM of the Neural network model for predicting your
signal peptides or both? Have you noticed how the
results from each model are almost always conflicting?
Even if they both predict a signal peptide they almost
always give different cleavage sites, often by only 1
or 2 amino acids.
If anyone knows whether one model is more reliable
than the other or has also encountered this problem I
would appreciate your feedback! I have emailed the
Signal P distributors countless times and never get a
reply.

Thanks!
-Kerrie Dunstan

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