BlastR-fast and accurate database searches for non-coding RNAs

被引:23
|
作者
Bussotti, Giovanni [1 ,2 ]
Raineri, Emanuele [1 ,2 ,3 ]
Erb, Ionas [1 ,2 ]
Zytnicki, Matthias [1 ,2 ,4 ]
Wilm, Andreas [5 ]
Beaudoing, Emmanuel [1 ,2 ,6 ]
Bucher, Philipp [7 ,8 ]
Notredame, Cedric [1 ,2 ]
机构
[1] CRG, Bioinformat & Genom Program, Barcelona 08003, Spain
[2] UPF, Barcelona 08003, Spain
[3] CNAG Ctr Nacl Anal Genom, E-08028 Barcelona, Spain
[4] URGI INRA Versailles, Dept Plant Breeding & Genet, F-78026 Versailles, France
[5] Univ Coll Dublin, Conway Inst Biomol & Biomed Sci, Dublin 4, Ireland
[6] Univ Lausanne, Ctr Integrat Genom, Genom Technol Facil, CH-1015 Lausanne, Switzerland
[7] Ecole Polytech Fed Lausanne, ISREC, Sch Life Sci, CH-1015 Lausanne, Switzerland
[8] SIB, CH-1015 Lausanne, Switzerland
基金
新加坡国家研究基金会;
关键词
SECONDARY STRUCTURE; SEQUENCE ALIGNMENT; NUCLEOTIDE; IDENTIFICATION; SUBSTITUTION; ALGORITHM; EVOLUTION; HOMOLOGS; ELEMENTS; MODELS;
D O I
10.1093/nar/gkr335
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We present and validate BlastR, a method for efficiently and accurately searching non-coding RNAs. Our approach relies on the comparison of di-nucleotides using BlosumR, a new log-odd substitution matrix. In order to use BlosumR for comparison, we recoded RNA sequences into protein-like sequences. We then showed that BlosumR can be used along with the BlastP algorithm in order to search non-coding RNA sequences. Using Rfam as a gold standard, we benchmarked this approach and show BlastR to be more sensitive than BlastN. We also show that BlastR is both faster and more sensitive than BlastP used with a single nucleotide log-odd substitution matrix. BlastR, when used in combination with WU-BlastP, is about 5% more accurate than WU-BlastN and about 50 times slower. The approach shown here is equally effective when combined with the NCBI-Blast package. The software is an open source freeware available from www.tcoffee.org/blastr.html.
引用
收藏
页码:6886 / 6895
页数:10
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