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- W2000557348 abstract "With the avalanche of genomic and proteomic data generated in the postgenomic age, it is highly desirable to develop automated methods for rapidly and effectively analyzing and predicting the structure, function, and other properties of DNA and protein. The machine learning methods have become an important strategy for the discovery of potential knowledge in genomics and proteomics. Researches in recent years have shown tremendous advances in the properties prediction of DNA fragments and protein sequences by various pattern recognition methods. These techniques provide economical and timesaving solutions for identifying the properties of DNA and protein. This special issue was hosted for the recent development of the application of machine learning methods in genomics and proteomics.In this special issue, five works focused on the protein classification. How to extract key features from a protein was a key step in the discrimination of protein class. B. Liu et al. proposed to use Position-Specific Score Matrix (PSSM) and Accessible Surface Area (ASA) to formulate protein samples. The hidden Markov support vector machine (HM-SVM) was employed to predict protein binding site. Simulation in fivefold cross-validation on a benchmark dataset including 1124 protein chains showed that their method is more accurate for protein binding site prediction than some state-of-the art methods. This method can also be applied in DNA binding site, vitamin binding site, and posttranslational modification of proteins.Based on chemical shift (CS) information derived from nuclear magnetic resonance (NMR), F. Yonge proposed a novel feature to predict protein supersecondary structures. The quadratic discriminant (QD) analysis was selected as the prediction algorithm. Overall accuracy in threefold cross-validation is 77.3% for predicting four types of supersecondary structures. According to the concept of pseudo amino acids, G.-L. Fan et al. proposed the average chemical shifts (ACS) composition and established an online webserver called acACS which was calculated from average chemical shift information and protein secondary structure. By using SVM as the classification algorithm, the acACS was used in the discrimination between acidic and alkaline enzymes and between bioluminescent and nonbioluminescent proteins. Encouraging results were achieved. The protein secondary structure, structure class, and disorder region can be predicted using the AC-based method.L. Nanni et al. proposed to combine different features to improve protein prediction. These features include amino acids composition, PSSM, and substitution matrix representation (SMR). Each feature is used to train a separate SVM. Total of 15 benchmark datasets were used to evaluate the performance of their proposed method. Comparative results show that the PSSM always produces good accuracies. However, no single descriptor is superior to all others across all test datasets. The major contribution in this paper is to propose an ensemble of classifiers for sequence-based protein classification.H. Lin et al. briefly reviewed the development of ion channel prediction using machine learning method. They initially introduced how to construct a valid and objective benchmark dataset to train and test the predictor. Subsequently, the mathematical descriptors were presented to formulate the ion channel sequences. Moreover, two feature selection techniques on how to optimize feature set were described. Finally, the support vector machine was suggested performing classification. The methods introduced in that review can be generalized into other protein prediction fields as well.The paper from P. Feng et al. was the unique work focused on DNA prediction using machine learning method. They proposed a novel descriptor called pseudo K-tuple nucleotide composition (PseKNC) to formulate the DNA sequences. The feature is calculated from K-tuple nucleotide composition and the structural correlation of DNA dinucleotides. Subsequently, the SVM was used to predict DNase I hypersensitive sites. The jackknife cross-validated accuracy is 83%, which is competitive with that of the existing method. This new descriptor can also be widely used in DNA regulatory elements prediction.Hao LinWei ChenRamu AnandakrishnanDariusz Plewczynski" @default.
- W2000557348 created "2016-06-24" @default.
- W2000557348 creator A5017541508 @default.
- W2000557348 creator A5021916927 @default.
- W2000557348 creator A5031644457 @default.
- W2000557348 creator A5041539298 @default.
- W2000557348 date "2015-01-01" @default.
- W2000557348 modified "2023-09-27" @default.
- W2000557348 title "Application of Machine Learning Method in Genomics and Proteomics" @default.
- W2000557348 cites W1550117682 @default.
- W2000557348 cites W1563088657 @default.
- W2000557348 cites W1607979445 @default.
- W2000557348 cites W1821507858 @default.
- W2000557348 cites W1906857739 @default.
- W2000557348 cites W1964904258 @default.
- W2000557348 cites W1966258773 @default.
- W2000557348 cites W1966991202 @default.
- W2000557348 cites W1969051510 @default.
- W2000557348 cites W1969299022 @default.
- W2000557348 cites W1972437239 @default.
- W2000557348 cites W1972848687 @default.
- W2000557348 cites W1974003283 @default.
- W2000557348 cites W1976133477 @default.
- W2000557348 cites W1977927254 @default.
- W2000557348 cites W1978736122 @default.
- W2000557348 cites W1980608565 @default.
- W2000557348 cites W1980897319 @default.
- W2000557348 cites W1981091069 @default.
- W2000557348 cites W1983065094 @default.
- W2000557348 cites W1984511561 @default.
- W2000557348 cites W1984907844 @default.
- W2000557348 cites W1986161806 @default.
- W2000557348 cites W1989298127 @default.
- W2000557348 cites W1992991025 @default.
- W2000557348 cites W1993791542 @default.
- W2000557348 cites W1996989509 @default.
- W2000557348 cites W1997996819 @default.
- W2000557348 cites W2002573639 @default.
- W2000557348 cites W2004524557 @default.
- W2000557348 cites W2008671051 @default.
- W2000557348 cites W2008708467 @default.
- W2000557348 cites W2011334977 @default.
- W2000557348 cites W2012273317 @default.
- W2000557348 cites W2014731953 @default.
- W2000557348 cites W2020816856 @default.
- W2000557348 cites W2020969907 @default.
- W2000557348 cites W2021408532 @default.
- W2000557348 cites W2024648909 @default.
- W2000557348 cites W2026029065 @default.
- W2000557348 cites W2026469255 @default.
- W2000557348 cites W2026710881 @default.
- W2000557348 cites W2029120587 @default.
- W2000557348 cites W2029904979 @default.
- W2000557348 cites W2030242529 @default.
- W2000557348 cites W2031292508 @default.
- W2000557348 cites W2031614119 @default.
- W2000557348 cites W2034070267 @default.
- W2000557348 cites W2036154117 @default.
- W2000557348 cites W2036956828 @default.
- W2000557348 cites W2042507562 @default.
- W2000557348 cites W2043976158 @default.
- W2000557348 cites W2044523575 @default.
- W2000557348 cites W2045092298 @default.
- W2000557348 cites W2046192291 @default.
- W2000557348 cites W2054068479 @default.
- W2000557348 cites W2058833671 @default.
- W2000557348 cites W2059971420 @default.
- W2000557348 cites W2059980912 @default.
- W2000557348 cites W2060596828 @default.
- W2000557348 cites W2063231296 @default.
- W2000557348 cites W2064984002 @default.
- W2000557348 cites W2066363861 @default.
- W2000557348 cites W2068922715 @default.
- W2000557348 cites W2074156599 @default.
- W2000557348 cites W2077467360 @default.
- W2000557348 cites W2078841894 @default.
- W2000557348 cites W2087985973 @default.
- W2000557348 cites W2088117005 @default.
- W2000557348 cites W2089047063 @default.
- W2000557348 cites W2090557416 @default.
- W2000557348 cites W2090958772 @default.
- W2000557348 cites W2092544746 @default.
- W2000557348 cites W2094840358 @default.
- W2000557348 cites W2097892623 @default.
- W2000557348 cites W2098105438 @default.
- W2000557348 cites W2098875971 @default.
- W2000557348 cites W2106386982 @default.
- W2000557348 cites W2108211735 @default.
- W2000557348 cites W2108898978 @default.
- W2000557348 cites W2109109045 @default.
- W2000557348 cites W2110813122 @default.
- W2000557348 cites W2113613985 @default.
- W2000557348 cites W2116089841 @default.
- W2000557348 cites W2117176840 @default.
- W2000557348 cites W2117403572 @default.
- W2000557348 cites W2117502874 @default.
- W2000557348 cites W2119792902 @default.
- W2000557348 cites W2124158580 @default.
- W2000557348 cites W2124557638 @default.
- W2000557348 cites W2125463451 @default.