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Efficient discovery of unique signatures on whole-genome EST databases
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Proceedings of the 2005 ACM symposium on Applied computing table of contents
Santa Fe, New Mexico
SESSION: Bioinformatics (BIO) table of contents
Pages: 100 - 104  
Year of Publication: 2005
ISBN:1-58113-964-0
Authors
Hsiao Ping Lee  National Tsing Hua University, Hsinchu, Taiwan, ROC
Tzu Fang Sheu  National Tsing Hua University, Hsinchu, Taiwan, ROC
Yin Te Tsai  Providence University, Shalu, Taiwan, ROC
Sponsor
SIGAPP: ACM Special Interest Group on Applied Computing
Publisher
ACM  New York, NY, USA
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ABSTRACT

Expressed Sequence Tags (EST) are widely used for the discovery of new genes, particularly those involved in human disease processes. A subsequence in an EST dataset is unique if it appears only in one EST sequence of the dataset but does not appear in any other EST sequence. The unique subsequences can be regarded as signatures that distinguish an EST from all the others, and provide valuable information for many applications, such as PCR primer designs and microarray experiments. The discoveries of unique signatures on large-scale EST datasets are previously computational challenges. In this paper, we propose two efficient algorithms to extract the unique signatures from EST databases. The algorithms perform impressive discovery efficiencies in the experiments on real human ESTs.


REFERENCES

Note: OCR errors may be found in this Reference List extracted from the full text article. ACM has opted to expose the complete List rather than only correct and linked references.

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Collaborative Colleagues:
Hsiao Ping Lee: colleagues
Tzu Fang Sheu: colleagues
Yin Te Tsai: colleagues