“…1AB for an example), with standard methods such as RNAfold [18], GTfold [32], and CyloFold [6]. Then they extract a lot of handcrafted features, some of which are Watson-Crick nucleotide pairing (A-U, C-G), loop length [43,42], sequence length [43], dinucleotide pair frequencies [43,20,42,4,34], trinucleotide pair frequencies (constituting 64 features) [43,20], melting temperature [43], mini-mum free energy [44,43,9]. These features are used as inputs to machine learning methods such as support vector machines (SVM) [42,4,46], random forests [34], neural networks [37,43,35,20] and hidden Markov models [1].…”