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Plant Physiol, March 2001, Vol. 125, pp. 1166-1174

Rice Bioinformatics. Analysis of Rice Sequence Data and Leveraging the Data to Other Plant Species1

Qiaoping Yuan, John Quackenbush, Razvan Sultana, Mihaela Pertea, Steven L. Salzberg, and C. Robin Buell*

The Institute for Genomic Research, 9712 Medical Center Drive, Rockville, Maryland 20850

Rice (Oryza sativa) is a model species for monocotyledonous plants, especially for members in the grass family. Several attributes such as small genome size, diploid nature, transformability, and establishment of genetic and molecular resources make it a tractable organism for plant biologists. With an estimated genome size of 430 Mb (Arumuganathan and Earle, 1991), it is feasible to obtain the complete genome sequence of rice using current technologies. An international effort has been established and is in the process of sequencing O. sativa spp. japonica var "Nipponbare" using a bacterial artificial chromosome/P1 artificial chromosome shotgun sequencing strategy. Annotation of the rice genome is performed using prediction-based and homology-based searches to identify genes. Annotation tools such as optimized gene prediction programs are being developed for rice to improve the quality of annotation. Resources are also being developed to leverage the rice genome sequence to partial genome projects such as expressed sequence tag projects, thereby maximizing the output from the rice genome project. To provide a low level of annotation for rice genomic sequences, we have aligned all rice bacterial artificial chromosome/P1 artificial chromosome sequences with The Institute of Genomic Research Gene Indices that are a set of nonredundant transcripts that are generated from nine public plant expressed sequence tag projects (rice, wheat, sorghum, maize, barley, Arabidopsis, tomato, potato, and barrel medic). In addition, we have used data from The Institute of Genomic Research Gene Indices and the Arabidopsis and Rice Genome Projects to identify putative orthologues and paralogues among these nine genomes.


1 This work was supported in part by the U.S. Department of Agriculture (grant no. 99-35317-8275 to C.R.B.), by the National Science Foundation (grant no. DBI998282 to C.R.B.), and by the U.S. Department of Energy (grant no. DE-FG02-99ER20357 to C.R.B.). This work was also supported by the U.S. Department of Energy (grant no. DE-FG02-99ER62852 to J.Q.) and by the U.S. National Science Foundation (grant nos. DBI-9983070, DBI-9813392, and DBI-9975866 to J.Q.). J.Q. was also supported in part by the National Science Foundation (grant no. KDI-9980088). S.L.S. and M.P. were supported in part by the National Institutes of Health (grant no. R01-LM06845) and by the National Science Foundation (grant nos. KDI-9980088 and IIS-9902923).

* Corresponding author; e-mail rbuell{at}tigr.org; fax 301-838-0208.

© 2001 American Society of Plant Physiologists



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