iRSpot-TNCPseAAC

swMATH22412MaRDI QIDQ34204FDOQ34204

Author name not available (Why is that?)

Cited In (31)

• SPrenylC-PseAAC: a sequence-based model developed via Chou's 5-steps rule and general PseAAC for identifying S-prenylation sites in proteins
• VR-BFDT: a variance reduction based binary fuzzy decision tree induction method for protein function prediction
• A two-layer classification framework for protein fold recognition
• A Hooke's law-based approach to protein folding rate
• Identifying 5-methylcytosine sites in RNA sequence using composite encoding feature into Chou's PseKNC
• IMem-2LSAAC: a two-level model for discrimination of membrane proteins and their types by extending the notion of SAAC into Chou's pseudo amino acid composition
• Machine learning approaches for discrimination of extracellular matrix proteins using hybrid feature space
• Using weighted features to predict recombination hotspots in \textit{Saccharomyces cerevisiae}
• Classify vertebrate hemoglobin proteins by incorporating the evolutionary information into the general PseAAC with the hybrid approach
• pSuc-Lys: predict lysine succinylation sites in proteins with PseAAC and ensemble random forest approach
• An effective haplotype assembly algorithm based on hypergraph partitioning
• An extension of fuzzy topological approach for comparison of genetic sequences
• Neural network and SVM classifiers accurately predict lipid binding proteins, irrespective of sequence homology
• Protein fold recognition by alignment of amino acid residues using kernelized dynamic time warping
• Discrimination of acidic and alkaline enzyme using Chou's pseudo amino acid composition in conjunction with probabilistic neural network model
• Prediction of \(\beta\)-lactamase and its class by Chou's pseudo-amino acid composition and support vector machine
• Chou's pseudo amino acid composition improves sequence-based antifreeze protein prediction
• fabp4 is central to eight obesity associated genes: a functional gene network-based polymorphic study
• Constructing a linear QSAR for some metabolizable drugs by human or pig flavin-containing monooxygenases using some molecular features selected by a genetic algorithm trained SVM
• A set of descriptors for identifying the protein-drug interaction in cellular networking
• Human proteins characterization with subcellular localizations
• RBSURFpred: modeling protein accessible surface area in real and binary space using regularized and optimized regression
• NucPosPred: predicting species-specific genomic nucleosome positioning via four different modes of general PseKNC
• pLoc\_bal-mGneg: predict subcellular localization of Gram-negative bacterial proteins by quasi-balancing training dataset and general PseAAC
• Communities in the iron superoxide dismutase amino acid network
• Fu-SulfPred: identification of protein S-sulfenylation sites by fusing forests via Chou's general PseAAC
• Analysis and prediction of ion channel inhibitors by using feature selection and Chou's general pseudo amino acid composition
• iMethyl-STTNC: identification of N\(^6\)-methyladenosine sites by extending the idea of SAAC into Chou's PseAAC to formulate RNA sequences
• Prediction of success for polymerase chain reactions using the Markov maximal order model and support vector machine
• iPPI-PseAAC(CGR): identify protein-protein interactions by incorporating chaos game representation into PseAAC
• Distribution bias of the sequence matching between exons and introns in exon joint and EJC binding region in \textit{C. elegans}

This page was built for software: iRSpot-TNCPseAAC