Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (178K) Freely available
Right arrow Supplementary Material
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (5)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Gopal, S.
Right arrow Articles by Gaasterland, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gopal, S.
Right arrow Articles by Gaasterland, T.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2003, Vol. 31, No. 20 5877-5885
© 2003 Oxford University Press

An organism-specific method to rank predicted coding regions in Trypanosoma brucei

Shuba Gopal*, George A. M. Cross1 and Terry Gaasterland

Laboratory of Computational Genomics and 1 Laboratory of Molecular Parasitology, The Rockefeller University, 1230 York Avenue, Box 250, New York, NY 10021, USA

*To whom correspondence should be addressed. Tel: +1 585 475 4498; Fax: +1 475 2533; Email: shuba{at}genomes.rockefeller.edu

Genome annotation in differently evolved organisms presents challenges because the lack of sequence-based homology limits the ability to determine the function of putative coding regions. To provide an alternative to annotation by sequence homology, we developed a method that takes advantage of unusual trypanosomatid biology and skews in nucleotide composition between coding regions and upstream regions to rank putative open reading frames based on the likelihood of coding. The method is 93% accurate when tested on known genes. We have applied our method to the full complement of open reading frames on Chromosome I of Trypanosoma brucei, and we can predict with high confidence that 226 putative coding regions are likely to be functional. Methods such as the one described here for discriminating true coding regions are critical for genome annotation when other sources of evidence for function are limited.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
H. Zhang, Y. Hou, L. Miranda, D. A. Campbell, N. R. Sturm, T. Gaasterland, and S. Lin
Spliced leader RNA trans-splicing in dinoflagellates
PNAS, March 13, 2007; 104(11): 4618 - 4623.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
T. N. Siegel, K. S. W. Tan, and G. A. M. Cross
Systematic Study of Sequence Motifs for RNA trans Splicing in Trypanosoma brucei
Mol. Cell. Biol., November 1, 2005; 25(21): 9586 - 9594.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.