Variations on RNA folding and alignment:: lessons from Benasque

被引:55
作者
Bompfuenewerer, Athanasius F.
Backofen, Rolf
Bernhart, Stephan H.
Hertel, Jana
Hofacker, Ivo L.
Stadler, Peter F.
Will, Sebastian
机构
[1] Univ Leipzig, Dept Comp Sci, Bioinformat Grp, D-04107 Leipzig, Germany
[2] Univ Leipzig, Interdisciplinary Ctr Bioinformat, D-04107 Leipzig, Germany
[3] Univ Vienna, Dept Theoret Chem, A-1090 Vienna, Austria
[4] Univ Freiburg, Dept Comp Sci, Bioinformat Grp, D-79110 Freiburg, Germany
[5] Santa Fe Inst, Santa Fe, NM 87501 USA
基金
奥地利科学基金会;
关键词
RNA folding; secondary structure alignment; dynamic programming;
D O I
10.1007/s00285-007-0107-5
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dynamic programming algorithms solve many standard problems of RNA bioinformatics in polynomial time. In this contribution we discuss a series of variations on these standard methods that implement refined biophysical models, such as a restriction of RNA folding to canonical structures, and an extension of structural alignments to an explicit scoring of stacking propensities. Furthermore, we demonstrate that a local structural alignment can be employed for ncRNA gene finding. In this context we discuss scanning variants for folding and alignment algorithms.
引用
收藏
页码:129 / 144
页数:16
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