Delila Server Entry Page
servers supply web access to Delila tools.
Presently they can be used to:
Results are displayed using
- Analyze sites in E. coli:
- Analyze human splice junctions and their mutations or polymorphisms
You may access the server either as a guest, in which case
you will have a limited number of allowed visits,
or as a registered user,
in which case you will have unlimited access.
To access as a guest, use:
If you are a registered user, please use that name.
THE SERVER IS NOT AVAILABLE.
There is a detailed online procedure that describes how
to obtain access to the Delila Servers:
Delila Server Orders
as of 2001 June 22)
Some aspects of the individual information theory programs are covered
by US patent 5867402. The programs may not be redistributed or used
without a signed agreement with the National Institutes of Health.
Please contact us at:
Note: commercial licenses must be done differently.
contact the Technology Transfer Branch.
Papers Citing This Web Server
These are papers by groups other than us.
Am J Hum Genet 2002 Apr;70(4):955-64
Newfoundland Rod-Cone Dystrophy, an
Early-Onset Retinal Dystrophy, Is Caused by
Splice-Junction Mutations in RLBP1.
Eichers ER, Green JS, Stockton DW, Jackman CS, Whelan J, McNamara
JA, Johnson GJ, Lupski JR, Katsanis N.
American Journal of Medical Genetics 109:291-297 (2002)
Searching for evidence of DFNB2,
Lisa M. Astuto, Philip M. Kelley, James W. Askew,
Michael D. Weston, Richard J.H. Smith, Abdulrahman F.
Alswaid, Mona Al-Rakaf, William J. Kim
origin: 2000 Nov 21
updated: 2012 Dec 11
U.S. Department of Health and Human Services
National Institutes of Health
National Cancer Institute