Predicting Gene Structures from Multiple RT-PCR Tests

被引:0
|
作者
Kovac, Jakub [1 ]
Vinar, Tomas [2 ]
Brejova, Brona [1 ]
机构
[1] Comenius Univ, Dept Comp Sci, Bratislava 84248, Slovakia
[2] Comenius Univ, Dept Appl Informat, Bratislava 84248, Slovakia
来源
关键词
gene finding; RT-PCR; NP-completeness; dynamic programming; splicing graph; IMPROVE;
D O I
暂无
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
It has been demonstrated that the use of additional information such as ESTs and protein homology can significantly improve accuracy of gene prediction. However, many sources of external information are still being omitted from consideration. Here, we investigate the use of product lengths from RT-PCR experiments in gene finding. We present hardness results and practical algorithms for several variants of the problem and apply our methods to a real RT-PCR data set in the Drosophila genome. We conclude that the use of RT-PCR data can improve the sensitivity of gene prediction and locate novel splicing variants.
引用
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页码:181 / +
页数:3
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