TY - JOUR
T1 - MethEvo
T2 - an accurate evolutionary information-based methylation site predictor
AU - Islam, Sadia
AU - Mugdha, Shafayat Bin Shabbir
AU - Dipta, Shubhashis Roy
AU - Arafat, Md Easin
AU - Shatabda, Swakkhar
AU - Alinejad-Rokny, Hamid
AU - Dehzangi, Iman
N1 - Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer-Verlag London Ltd., part of Springer Nature.
PY - 2024/1
Y1 - 2024/1
N2 - Post Translational Modification (PTM) plays an essential role in the biological and molecular mechanisms. They are also considered as a vital element in cell signaling and networking pathways. Among different PTMs, Methylation is regarded as one of the most important types. Methylation plays a crucial role in maintaining the dynamic balance, stability, and remodeling of chromatins. Methylation also leads to different abnormalities in cells and is responsible for many serious diseases. Methylation can be detected by experimental approaches such as methylation-specific antibodies, mass spectrometry, or characterizing methylation sites using the radioactive labeling method. However, these approaches are time-consuming and costly. Therefore, there is a demand for fast and accurate computational techniques to solve these issues. This study proposes a novel machine learning approach called MethEvo to predict methylation sites in proteins. To build this model, we use an evolutionary-based bi-gram profile approach to extract features. We also use SVM as our classification technique to build MethEvo. Our results demonstrate that MethEvo achieves 98.7%, 98.8%, 98.4%, and 0.974 in terms of accuracy, specificity, sensitivity, and Matthews Correlation Coefficient (MCC). MethEvo and its source code are publicly available at: https://github.com/islamsadia88/MethEvo.
AB - Post Translational Modification (PTM) plays an essential role in the biological and molecular mechanisms. They are also considered as a vital element in cell signaling and networking pathways. Among different PTMs, Methylation is regarded as one of the most important types. Methylation plays a crucial role in maintaining the dynamic balance, stability, and remodeling of chromatins. Methylation also leads to different abnormalities in cells and is responsible for many serious diseases. Methylation can be detected by experimental approaches such as methylation-specific antibodies, mass spectrometry, or characterizing methylation sites using the radioactive labeling method. However, these approaches are time-consuming and costly. Therefore, there is a demand for fast and accurate computational techniques to solve these issues. This study proposes a novel machine learning approach called MethEvo to predict methylation sites in proteins. To build this model, we use an evolutionary-based bi-gram profile approach to extract features. We also use SVM as our classification technique to build MethEvo. Our results demonstrate that MethEvo achieves 98.7%, 98.8%, 98.4%, and 0.974 in terms of accuracy, specificity, sensitivity, and Matthews Correlation Coefficient (MCC). MethEvo and its source code are publicly available at: https://github.com/islamsadia88/MethEvo.
KW - Bi-gram profile
KW - Evolutionary-based features
KW - Methylation
KW - Post translational modification
KW - Support vector machine
UR - http://www.scopus.com/inward/record.url?scp=85138513581&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85138513581&partnerID=8YFLogxK
U2 - 10.1007/s00521-022-07738-9
DO - 10.1007/s00521-022-07738-9
M3 - Article
AN - SCOPUS:85138513581
SN - 0941-0643
VL - 36
SP - 201
EP - 212
JO - Neural Computing and Applications
JF - Neural Computing and Applications
IS - 1
ER -