Literature DB >> 17933013

Stem kernels for RNA sequence analyses.

Yasubumi Sakakibara1, Kris Popendorf, Nana Ogawa, Kiyoshi Asai, Kengo Sato.   

Abstract

Several computational methods based on stochastic context-free grammars have been developed for modeling and analyzing functional RNA sequences. These grammatical methods have succeeded in modeling typical secondary structures of RNA, and are used for structural alignment of RNA sequences. However, such stochastic models cannot sufficiently discriminate member sequences of an RNA family from nonmembers and hence detect noncoding RNA regions from genome sequences. A novel kernel function, stem kernel, for the discrimination and detection of functional RNA sequences using support vector machines (SVMs) is proposed. The stem kernel is a natural extension of the string kernel, specifically the all-subsequences kernel, and is tailored to measure the similarity of two RNA sequences from the viewpoint of secondary structures. The stem kernel examines all possible common base pairs and stem structures of arbitrary lengths, including pseudoknots between two RNA sequences, and calculates the inner product of common stem structure counts. An efficient algorithm is developed to calculate the stem kernels based on dynamic programming. The stem kernels are then applied to discriminate members of an RNA family from nonmembers using SVMs. The study indicates that the discrimination ability of the stem kernel is strong compared with conventional methods. Furthermore, the potential application of the stem kernel is demonstrated by the detection of remotely homologous RNA families in terms of secondary structures. This is because the string kernel is proven to work for the remote homology detection of protein sequences. These experimental results have convinced us to apply the stem kernel in order to find novel RNA families from genome sequences.

Mesh:

Substances:

Year:  2007        PMID: 17933013     DOI: 10.1142/s0219720007003028

Source DB:  PubMed          Journal:  J Bioinform Comput Biol        ISSN: 0219-7200            Impact factor:   1.122


  6 in total

1.  Robust and accurate prediction of noncoding RNAs from aligned sequences.

Authors:  Yutaka Saito; Kengo Sato; Yasubumi Sakakibara
Journal:  BMC Bioinformatics       Date:  2010-10-15       Impact factor: 3.169

Review 2.  Informatic resources for identifying and annotating structural RNA motifs.

Authors:  Ajish D George; Scott A Tenenbaum
Journal:  Mol Biotechnol       Date:  2008-11-01       Impact factor: 2.695

3.  Genome-wide searching with base-pairing kernel functions for noncoding RNAs: computational and expression analysis of snoRNA families in Caenorhabditis elegans.

Authors:  Kensuke Morita; Yutaka Saito; Kengo Sato; Kotaro Oka; Kohji Hotta; Yasubumi Sakakibara
Journal:  Nucleic Acids Res       Date:  2009-01-07       Impact factor: 16.971

4.  Directed acyclic graph kernels for structural RNA analysis.

Authors:  Kengo Sato; Toutai Mituyama; Kiyoshi Asai; Yasubumi Sakakibara
Journal:  BMC Bioinformatics       Date:  2008-07-22       Impact factor: 3.169

5.  Software.ncrna.org: web servers for analyses of RNA sequences.

Authors:  Kiyoshi Asai; Hisanori Kiryu; Michiaki Hamada; Yasuo Tabei; Kengo Sato; Hiroshi Matsui; Yasubumi Sakakibara; Goro Terai; Toutai Mituyama
Journal:  Nucleic Acids Res       Date:  2008-04-25       Impact factor: 16.971

6.  Accurate Classification of RNA Structures Using Topological Fingerprints.

Authors:  Jiajie Huang; Kejie Li; Michael Gribskov
Journal:  PLoS One       Date:  2016-10-18       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.