Knotify+: Toward the Prediction of RNA H-Type Pseudoknots, Including Bulges and Internal Loops

The accurate “base pairing” in RNA molecules, which leads to the prediction of RNA secondary structures, is crucial in order to explain unknown biological operations. Recently, COVID-19, a widespread disease, has caused many deaths, affecting humanity in an unprecedented way. SARS-CoV-2, a single-st...

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Main Authors: Evangelos Makris, Angelos Kolaitis, Christos Andrikos, Vrettos Moulos, Panayiotis Tsanakas, Christos Pavlatos
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/13/2/308
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author Evangelos Makris
Angelos Kolaitis
Christos Andrikos
Vrettos Moulos
Panayiotis Tsanakas
Christos Pavlatos
author_facet Evangelos Makris
Angelos Kolaitis
Christos Andrikos
Vrettos Moulos
Panayiotis Tsanakas
Christos Pavlatos
author_sort Evangelos Makris
collection DOAJ
description The accurate “base pairing” in RNA molecules, which leads to the prediction of RNA secondary structures, is crucial in order to explain unknown biological operations. Recently, COVID-19, a widespread disease, has caused many deaths, affecting humanity in an unprecedented way. SARS-CoV-2, a single-stranded RNA virus, has shown the significance of analyzing these molecules and their structures. This paper aims to create a pioneering framework in the direction of predicting specific RNA structures, leveraging syntactic pattern recognition. The proposed framework, Knotify+, addresses the problem of predicting H-type pseudoknots, including bulges and internal loops, by featuring the power of context-free grammar (CFG). We combine the grammar’s advantages with maximum base pairing and minimum free energy to tackle this ambiguous task in a performant way. Specifically, our proposed methodology, Knotify+, outperforms state-of-the-art frameworks with regards to its accuracy in core stems prediction. Additionally, it performs more accurately in small sequences and presents a comparable accuracy rate in larger ones, while it requires a smaller execution time compared to well-known platforms. The Knotify+ source code and implementation details are available as a public repository on GitHub.
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spelling doaj.art-0e69ef3d61b84719be7c6ebab58111752023-11-16T19:23:20ZengMDPI AGBiomolecules2218-273X2023-02-0113230810.3390/biom13020308Knotify+: Toward the Prediction of RNA H-Type Pseudoknots, Including Bulges and Internal LoopsEvangelos Makris0Angelos Kolaitis1Christos Andrikos2Vrettos Moulos3Panayiotis Tsanakas4Christos Pavlatos5School of Electrical and Computer Engineering, National Technical University of Athens, 9 Iroon Polytechniou St., 15780 Athens, GreeceSchool of Electrical and Computer Engineering, National Technical University of Athens, 9 Iroon Polytechniou St., 15780 Athens, GreeceSchool of Electrical and Computer Engineering, National Technical University of Athens, 9 Iroon Polytechniou St., 15780 Athens, GreeceSchool of Electrical and Computer Engineering, National Technical University of Athens, 9 Iroon Polytechniou St., 15780 Athens, GreeceSchool of Electrical and Computer Engineering, National Technical University of Athens, 9 Iroon Polytechniou St., 15780 Athens, GreeceHellenic Air Force Academy, Dekelia Air Base, Acharnes, 13671 Athens, GreeceThe accurate “base pairing” in RNA molecules, which leads to the prediction of RNA secondary structures, is crucial in order to explain unknown biological operations. Recently, COVID-19, a widespread disease, has caused many deaths, affecting humanity in an unprecedented way. SARS-CoV-2, a single-stranded RNA virus, has shown the significance of analyzing these molecules and their structures. This paper aims to create a pioneering framework in the direction of predicting specific RNA structures, leveraging syntactic pattern recognition. The proposed framework, Knotify+, addresses the problem of predicting H-type pseudoknots, including bulges and internal loops, by featuring the power of context-free grammar (CFG). We combine the grammar’s advantages with maximum base pairing and minimum free energy to tackle this ambiguous task in a performant way. Specifically, our proposed methodology, Knotify+, outperforms state-of-the-art frameworks with regards to its accuracy in core stems prediction. Additionally, it performs more accurately in small sequences and presents a comparable accuracy rate in larger ones, while it requires a smaller execution time compared to well-known platforms. The Knotify+ source code and implementation details are available as a public repository on GitHub.https://www.mdpi.com/2218-273X/13/2/308H-type pseudoknot structureRNAbulgesinternal loopsparserCFG
spellingShingle Evangelos Makris
Angelos Kolaitis
Christos Andrikos
Vrettos Moulos
Panayiotis Tsanakas
Christos Pavlatos
Knotify+: Toward the Prediction of RNA H-Type Pseudoknots, Including Bulges and Internal Loops
Biomolecules
H-type pseudoknot structure
RNA
bulges
internal loops
parser
CFG
title Knotify+: Toward the Prediction of RNA H-Type Pseudoknots, Including Bulges and Internal Loops
title_full Knotify+: Toward the Prediction of RNA H-Type Pseudoknots, Including Bulges and Internal Loops
title_fullStr Knotify+: Toward the Prediction of RNA H-Type Pseudoknots, Including Bulges and Internal Loops
title_full_unstemmed Knotify+: Toward the Prediction of RNA H-Type Pseudoknots, Including Bulges and Internal Loops
title_short Knotify+: Toward the Prediction of RNA H-Type Pseudoknots, Including Bulges and Internal Loops
title_sort knotify toward the prediction of rna h type pseudoknots including bulges and internal loops
topic H-type pseudoknot structure
RNA
bulges
internal loops
parser
CFG
url https://www.mdpi.com/2218-273X/13/2/308
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