OSIRIS

Record added by Jurg Ott (the original Rockefeller list)

Version

1.1

Description

OSIRIS is a tool for the retrieval of articles from MEDLINE related to the sequence variants reported for a human gene. The variations considered are single nucleotide polymorphisms (SNPs), insertion/deletion polymorphisms (indel), microsatellite, and named variations (e.g. Alu sequences).

Author

  • Julio Bonis

  • Laura Ines Furlong Ferran Sanz (University of Pompeu Fabra, Spain) (email: fsanz@imim.es)

    URL

    http://ibi.imim.es/osirisform.html

    Reference

    Bonis, Furlong, Sanz (2006), “OSIRIS: a tool for retrieving literature about sequence variants”, Bioinformatics, 22(20):2567-2569.