| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 1934230 | Biochemical and Biophysical Research Communications | 2008 | 4 Pages | 
Abstract
												Alternative splicing is generally accepted as a mechanism that explains the discrepancy between the number of genes and proteins. We used peptide mass fingerprinting with a theoretical database and scoring method to discover and identify alternative splicing isoforms. Our theoretical database was built using published alternative splicing databases such as ECgene, H-DBAS, and TISA. According to our theoretical database of 190,529 isoforms, 37% of human genes have multiple isoforms. The isoforms produced from a gene partially share common peptide fragments because they have common exons, making it difficult to distinguish isoforms. Therefore, we developed a new method that effectively distinguishes a true isoform among multiple isoforms in a gene. In order to evaluate our algorithm, we made test sets for 4226 protein isoforms extracted from our theoretical database randomly. Consequently, 94% of true isoforms were identified by our scoring algorithm.
											Keywords
												
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											Authors
												Seung-Won Lee, Jae-Pil Choi, Hyun-Jin Kim, Ji-Man Hong, Cheol-Goo Hur, 
											