iPTM-mLys
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IPTM-mLys
Cited in
(only showing first 100 items - show all)- ESA-UbiSite
- iDNA4mC
- Fu-SulfPred
- HMMBinder
- XGBFEMF
- Meta-4mCpred
- 4mCPred
- Deep4mC
- iDNA-MS
- Identify Gram-negative bacterial secreted protein types by incorporating different modes of PSSM into Chou's general PseAAC via Kullback-Leibler divergence
- Characterization of BioPlex network by topological properties
- Prediction of metastasis in advanced colorectal carcinomas using CGH data
- BlaPred: predicting and classifying \(\beta\)-lactamase using a 3-tier prediction system via Chou's general PseAAC
- pLoc\_bal-mGneg: predict subcellular localization of Gram-negative bacterial proteins by quasi-balancing training dataset and general PseAAC
- iRNA-PseKNC(2methyl): identify RNA 2'-O-methylation sites by convolution neural network and Chou's pseudo components
- Predicting protein sub-Golgi locations by combining functional domain enrichment scores with pseudo-amino acid compositions
- Prediction of S-sulfenylation sites using mRMR feature selection and fuzzy support vector machine algorithm
- Predicting apoptosis protein subcellular localization by integrating auto-cross correlation and PSSM into Chou's PseAAC
- 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
- Effective DNA binding protein prediction by using key features via Chou's general PseAAC
- iPPI-PseAAC(CGR): identify protein-protein interactions by incorporating chaos game representation into PseAAC
- Analysis and prediction of animal toxins by various Chou's pseudo components and reduced amino acid compositions
- pSSbond-PseAAC: prediction of disulfide bonding sites by integration of PseAAC and statistical moments
- iPHLoc-ES: identification of bacteriophage protein locations using evolutionary and structural features
- Sequence-based discrimination of protein-RNA interacting residues using a probabilistic approach
- Identifying N\(^6\)-methyladenosine sites using extreme gradient boosting system optimized by particle swarm optimizer
- SPrenylC-PseAAC: a sequence-based model developed via Chou's 5-steps rule and general PseAAC for identifying S-prenylation sites in proteins
- Dforml(KNN)-PseAAC: detecting formylation sites from protein sequences using K-nearest neighbor algorithm via Chou's 5-step rule and pseudo components
- Predicting protein submitochondrial locations by incorporating the pseudo-position specific scoring matrix into the general Chou's pseudo-amino acid composition
- 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
- Predicting membrane protein types by incorporating a novel feature set into Chou's general PseAAC
- Highly accurate prediction of protein self-interactions by incorporating the average block and PSSM information into the general PseAAC
- LogitBoost
- pSuc-Lys
- iLM-2L
- iEnhancer-2L
- 2D-MH
- AFP-Pred
- UniProt
- iDNA-Prot
- iPro54-PseKNC
- iPPI-Esml
- iDHS-EL
- iSS-Hyb-mRMR
- iPPBS-Opt
- iSuc-PseOpt
- iMethyl-PseAAC
- iRSpot-PseDNC
- iRNA-Methyl
- iNitro-Tyr
- iSNO-PseAAC
- iSNO-AAPair
- Pse-in-One
- ngLOC
- Prnam-PC
- PseKNC
- DORAEMON
- Pse-analysis
- iACP
- iCar-PseCp
- iHyd-PseCp
- iPhos-PseEvo
- iPhos-PseEn
- iOri-Human
- pSumo-CD
- RVMAB
- iRNA-AI
- iRNA-PseColl
- iATC-mHyb
- iRNA-2methyl
- iRNAm5C-PseDNC
- iPreny-PseAAC
- pLoc-mAnimal
- pLoc-mVirus
- pLoc-mEuk
- DPP-PseAAC
- POSSUM
- iRSpot-EL
- iPromoter-2L
- NucPosPred
- PSLDoc
- iHSP-PseRAAAC
- iKcr-PseEns
- iTIS-PseKNC
- OOgenesis_Pred
- PINGU
- PREvaIL
- MitProt-Pred
- pLoc-mGneg
- pLoc-mPlant
- iNuc-STNC
- iROS-gPseKNC
- Unb-DPC
- Phage_Finder
- PHYPred
- PHACTS
- Phast
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