TY - GEN
T1 - Improvement of structure conservation index with centroid estimators
AU - Okada, Yohei
AU - Sato, Kengo
AU - Sakakibara, Yasubumi
PY - 2010
Y1 - 2010
N2 - RNAz, a support vector machine (SVM) approach for identifying functional non-coding RNAs (ncRNAs), has been proven to be one of the most accurate tools for this goal. Among the measurements used in RNAz, the Structure Conservation Index (SCI) which evaluates the evolutionary conservation of RNA secondary structures in terms of folding energies, has been reported to have an extremely high discrimination capability. However, for practical use of RNAz on the genome-wide search, a relatively high false discovery rate has unfortunately been estimated. It is conceivable that multiple alignments produced by a standard aligner that does not consider any secondary structures are not suitable for identifying ncRNAs in some cases and incur high false discovery rate. In this study, we propose C-SCI, an improved measurement based on the SCI applying γ-centroid estimators to incorporate the robustness against low quality multiple alignments. Our experiments show that the C-SCI achieves higher accuracy than the original SCI for not only human-curated structural alignments but also low quality alignments produced by CLUSTAL W. Furthermore, the accuracy of the C-SCI on CLUSTAL W alignments is comparable with that of the original SCI on structural alignments generated with RAF for which 4.7-fold expensive computational time is required on average.
AB - RNAz, a support vector machine (SVM) approach for identifying functional non-coding RNAs (ncRNAs), has been proven to be one of the most accurate tools for this goal. Among the measurements used in RNAz, the Structure Conservation Index (SCI) which evaluates the evolutionary conservation of RNA secondary structures in terms of folding energies, has been reported to have an extremely high discrimination capability. However, for practical use of RNAz on the genome-wide search, a relatively high false discovery rate has unfortunately been estimated. It is conceivable that multiple alignments produced by a standard aligner that does not consider any secondary structures are not suitable for identifying ncRNAs in some cases and incur high false discovery rate. In this study, we propose C-SCI, an improved measurement based on the SCI applying γ-centroid estimators to incorporate the robustness against low quality multiple alignments. Our experiments show that the C-SCI achieves higher accuracy than the original SCI for not only human-curated structural alignments but also low quality alignments produced by CLUSTAL W. Furthermore, the accuracy of the C-SCI on CLUSTAL W alignments is comparable with that of the original SCI on structural alignments generated with RAF for which 4.7-fold expensive computational time is required on average.
KW - centroid estimators
KW - non-coding RNAs
KW - structure conservation index
UR - https://www.scopus.com/pages/publications/79551474846
UR - https://www.scopus.com/pages/publications/79551474846#tab=citedBy
M3 - Conference contribution
C2 - 19908361
AN - SCOPUS:79551474846
SN - 9814295299
SN - 9789814295291
T3 - Pacific Symposium on Biocomputing 2010, PSB 2010
SP - 88
EP - 97
BT - Pacific Symposium on Biocomputing 2010, PSB 2010
PB - World Scientific
T2 - 15th Pacific Symposium on Biocomputing, PSB 2010
Y2 - 4 January 2010 through 8 January 2010
ER -