sequence walker for human donor splice junctions

Delila Server Entry Page


The Delila servers supply web access to Delila tools. They can be used to:

Results are displayed using sequence walkers.

US patent 5867402

Some aspects of the individual information theory programs are covered by US patent 5867402. However, the patent has been abandoned, so you are free to use the programs as open source.

Papers Citing This (former) Web Server

These are papers by groups other than us.

  1. 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.
  2. 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

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Schneider Lab

origin: 2000 Nov 21
updated: 2022 Aug 01
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