The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs

被引:1901
作者
Schattner, P
Brooks, AN
Lowe, TM
机构
[1] Univ Calif Santa Cruz, Dept Biomol Engn, Santa Cruz, CA 95064 USA
[2] Univ Calif Santa Cruz, UCSC RNA Ctr, Santa Cruz, CA 95064 USA
[3] Univ Calif San Diego, Div Biol Sci, Cell & Dev Biol Sect, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Ctr Genet Mol, La Jolla, CA 92093 USA
关键词
D O I
10.1093/nar/gki366
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
Transfer RNAs (tRNAs) and small nucleolar RNAs (snoRNAs) are two of the largest classes of non-protein-coding RNAs. Conventional gene finders that detect protein-coding genes do not find tRNA and snoRNA genes because they lack the codon structure and statistical signatures of protein-coding genes. Previously, we developed tRNAscanSE, snoscan and snoGPS for the detection of tRNAs, methylation-guide snoRNAs and pseudouridylation-guide snoRNAs, respectively. tRNAscan-SE is routinely applied to completed genomes, resulting in the identification of thousands of tRNA genes. Snoscan has successfully detected methylationguide snoRNAs in a variety of eukaryotes and archaea, and snoGPS has identified novel pseudouridylation- guide snoRNAs in yeast and mammals. Although these programs have been quite successful at RNA gene detection, their use has been limited by the need to install and configure the software packages on UNIX workstations. Here, we describe online implementations of these RNA detection tools that make these programs accessible to a wider range of research biologists. The tRNAscan-SE, snoscan and snoGPS servers are available at http://lowelab. ucsc. edu/ tRNAscanSE/,http://lowelab. ucsc.edu/snoscan/and http://lowelab.ucsc.edu/snoGPS/, respectively.
引用
收藏
页码:W686 / W689
页数:4
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