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Prediction of MicroRNA Precursors Using Parsimonious Feature Sets
Author(s) -
Petra Stepanowsky,
Éric Levy,
Jihoon Kim,
Xiaoqian Jiang,
Lucila OhnoMachado
Publication year - 2014
Publication title -
cancer informatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.606
H-Index - 31
ISSN - 1176-9351
DOI - 10.4137/cin.s13877
Subject(s) - random forest , microrna , computer science , feature selection , feature (linguistics) , artificial intelligence , computational biology , identification (biology) , set (abstract data type) , data mining , pattern recognition (psychology) , bioinformatics , machine learning , biology , gene , genetics , philosophy , botany , programming language , linguistics
MicroRNAs (miRNAs) are a class of short noncoding RNAs that regulate gene expression through base pairing with messenger RNAs. Due to the interest in studying miRNA dysregulation in disease and limits of validated miRNA references, identification of novel miRNAs is a critical task. The performance of different models to predict novel miRNAs varies with the features chosen as predictors. However, no study has systematically compared published feature sets. We constructed a comprehensive feature set using the minimum free energy of the secondary structure of precursor miRNAs, a set of nucleotide-structure triplets, and additional extracted sequence and structure characteristics. We then compared the predictive value of our comprehensive feature set to those from three previously published studies, using logistic regression and random forest classifiers. We found that classifiers containing as few as seven highly predictive features are able to predict novel precursor miRNAs as well as classifiers that use larger feature sets. In a real data set, our method correctly identified the holdout miRNAs relevant to renal cancer.

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