Identifier Index

[ A B C D E F G H I J K L M N O P Q R S T U V W X Y Z _ ]

N

nActs (in RunDetails)	negative (in ML.SLT.Risk)	not_equal (in ML.Cluster.ClusterUtils)
NaiveBayes (in ML)	negative (in ML.ScreenComposite)	not_equal (in ML.Cluster.ClusterVis)
NaiveBayesClassifier (in ML.NaiveBayes.ClassificationModel)	negative (in ML.files)	not_equal (in ML.Cluster.Clusters)
name (in Chem.AvailDescriptors)	negative (in PySVD.SVDPack)	not_equal (in ML.Cluster.Murtagh)
name (in Font)	negative (in PySVD.SVDSimilarity)	not_equal (in ML.Cluster.Resemblance)
name (in Chem.EState.EState_VSA)	NetNode (in ML.Neural)	not_equal (in ML.Cluster.Standardize)
name (in Chem.Fragments)	NetNode (in ML.Neural.NetNode)	not_equal (in ML.Composite.AdjustComposite)
nameCol (in RunDetails)	Network (in ML.Neural)	not_equal (in ML.Composite.BayesComposite)
NameModel() (in SigTreeNode)	Network (in ML.Neural.Network)	not_equal (in ML.Composite.Composite)
NameModel() (in KNNClassificationModel)	Neural (in ML)	not_equal (in ML.Data.MLData)
NameModel() (in KNNRegressionModel)	next() (in FastSDMolSupplier)	not_equal (in ML.Data.Quantize)
NameModel() (in NaiveBayesClassifier)	next() (in DbFpSupplier)	not_equal (in ML.Data.Stats)
nameTable (in Chem.PeriodicTable')	next() (in ThresholdScreener)	not_equal (in ML.Data.Transforms)
NameTree() (in TreeNode)	next() (in TopNScreener)	not_equal (in ML.DecTree.BuildQuantTree)
nBits (in RunDetails)	next() (in MolSupplier)	not_equal (in ML.DecTree.BuildSigTree)
nbrCount (in SubshapeBuilder)	next() (in SDMolSupplier)	not_equal (in ML.DecTree.CrossValidate)
nDistPointDict (in Chem.Pharm2D.Utils)	next() (in SmilesMolSupplier)	not_equal (in ML.DecTree.Forest)
nDumped (in Chem.ChemUtils.TemplateExpand)	next() (in TDTMolSupplier)	not_equal (in ML.DecTree.ID3)
Negate() (in FilterNode)	next() (in DbResultSet)	not_equal (in ML.DecTree.PruneTree)
negative (in Chem.BuildFragmentCatalog)	next() (in RandomAccessDbResultSet)	not_equal (in ML.DecTree.randomforest)
negative (in Chem.Crippen)	next() (in FilterNode)	not_equal (in ML.EnrichPlot)
negative (in Chem.EState.EState)	next() (in VLibNode)	not_equal (in ML.GrowComposite)
negative (in Chem.EState)	next() (in DbMolSupplyNode)	not_equal (in ML.InfoTheory.BitClusterer)
negative (in Chem.Features.FeatDirUtils)	next() (in DbPickleSupplyNode)	not_equal (in ML.InfoTheory.BitRank)
negative (in Chem.Features.FeatDirUtilsRD)	next() (in _lazyDataSeq)	not_equal (in ML.InfoTheory.entropy)
negative (in Chem.Fingerprints.ClusterMols)	next() (in SDSupplyNode)	not_equal (in ML.KNN.CrossValidate)
negative (in Chem.FragmentCatalog)	next() (in SmilesSupplyNode)	not_equal (in ML.MLUtils.VoteImg)
negative (in Chem.GraphDescriptors)	next() (in OutputNode)	not_equal (in ML.NaiveBayes.ClassificationModel)
negative (in Chem.Graphs)	next() (in SupplyNode)	not_equal (in ML.Neural.ActFuncs)
negative (in Chem.MolSurf)	next() (in TransformNode)	not_equal (in ML.Neural.NetNode)
negative (in Chem.Pharm2D.Signature)	NextItem() (in ForwardDbFpSupplier)	not_equal (in ML.Neural.Network)
negative (in Chem.Pharm2D.Utils)	NextItem() (in RandomAccessDbFpSupplier)	not_equal (in ML.Neural.Trainers)
negative (in Chem.Pharm3D.EmbedLib)	NextMol() (in ForwardDbMolSupplier)	not_equal (in ML.SLT.Risk)
negative (in Chem.Pharm3D.Pharmacophore)	NextMol() (in RandomAccessDbMolSupplier)	not_equal (in ML.ScreenComposite)
negative (in ML.AnalyzeComposite)	NextMol() (in MolSupplier)	not_equal (in ML.files)
negative (in ML.BuildComposite)	NHOHCount() (in Chem.Lipinski)	not_equal (in PySVD.SVDPack)
negative (in ML.Cluster.Butina)	NHOHSmarts (in Chem.Lipinski)	not_equal (in PySVD.SVDSimilarity)
negative (in ML.Cluster.ClusterUtils)	noCarbonSymbols (in MolDrawing)	nPerClass (in BitGainsInfo)
negative (in ML.Cluster.ClusterVis)	NOCount() (in Chem.Lipinski)	nPointDistDict (in Chem.Pharm2D.Utils)
negative (in ML.Cluster.Clusters)	NOCountSmarts (in Chem.Lipinski)	numAtomPairFingerprintBits (in AtomPairsParameters)
negative (in ML.Cluster.Murtagh)	Node (in VLib)	NumAtomRings() (in RingInfo)
negative (in ML.Cluster.Resemblance)	nodeColor (in VisOpts)	NumBitsInCommon() (in DataStructs.cDataStructs)
negative (in ML.Cluster.Standardize)	NodeLib (in VLib)	NumBondRings() (in RingInfo)
negative (in ML.Composite.AdjustComposite)	nodeRad (in VisOpts)	numBranchBits (in AtomPairsParameters)
negative (in ML.Composite.BayesComposite)	NoMerge (in DirMergeMode)	NumChildren() (in VectCollection)
negative (in ML.Composite.Composite)	NoMerge (in MergeMetric)	NumCombinations() (in Chem.Pharm2D.Utils)
negative (in ML.Data.MLData)	NONE (in BondDir)	Numerics
negative (in ML.Data.Quantize)	NORMAL (in Chem.Features.ShowFeats)	numericTypes (in ML.Data.MLData)
negative (in ML.Data.Stats)	Normalize() (in Point2D)	numFeatThresh (in SubshapeAligner)
negative (in ML.Data.Transforms)	Normalize() (in Point3D)	numFpBits (in Chem.AtomPairs.Pairs)
negative (in ML.DecTree.BuildQuantTree)	Normalize() (in PointND)	NumHAcceptors() (in Chem.Lipinski)
negative (in ML.DecTree.BuildSigTree)	not_equal (in Chem.BuildFragmentCatalog)	NumHDonors() (in Chem.Lipinski)
negative (in ML.DecTree.CrossValidate)	not_equal (in Chem.Crippen)	NumHeteroatoms() (in Chem.Lipinski)
negative (in ML.DecTree.Forest)	not_equal (in Chem.EState.EState)	numMols (in RunDetails)
negative (in ML.DecTree.ID3)	not_equal (in Chem.EState)	NumMols() (in SDWriter)
negative (in ML.DecTree.PruneTree)	not_equal (in Chem.Features.FeatDirUtils)	NumMols() (in SmilesWriter)
negative (in ML.DecTree.randomforest)	not_equal (in Chem.Features.FeatDirUtilsRD)	NumMols() (in TDTWriter)
negative (in ML.EnrichPlot)	not_equal (in Chem.Fingerprints.ClusterMols)	NumOnBits() (in BitVect)
negative (in ML.GrowComposite)	not_equal (in Chem.FragmentCatalog)	NumOnBits() (in SparseBitVect)
negative (in ML.InfoTheory.BitClusterer)	not_equal (in Chem.GraphDescriptors)	numPathBits (in Chem.AtomPairs.Pairs)
negative (in ML.InfoTheory.BitRank)	not_equal (in Chem.Graphs)	numPathBits (in AtomPairsParameters)
negative (in ML.InfoTheory.entropy)	not_equal (in Chem.MolSurf)	numPiBits (in AtomPairsParameters)
negative (in ML.KNN.CrossValidate)	not_equal (in Chem.Pharm2D.Signature)	NumPiElectrons() (in Chem.AtomPairs.Utils)
negative (in ML.MLUtils.VoteImg)	not_equal (in Chem.Pharm2D.Utils)	NumRings() (in RingInfo)
negative (in ML.NaiveBayes.ClassificationModel)	not_equal (in Chem.Pharm3D.EmbedLib)	NumRotatableBonds() (in Chem.Lipinski)
negative (in ML.Neural.ActFuncs)	not_equal (in Chem.Pharm3D.Pharmacophore)	numTable (in Chem.PeriodicTable')
negative (in ML.Neural.NetNode)	not_equal (in ML.AnalyzeComposite)	numTypeBits (in AtomPairsParameters)
negative (in ML.Neural.Network)	not_equal (in ML.BuildComposite)	NumValenceElectrons() (in Chem.Descriptors)
negative (in ML.Neural.Trainers)	not_equal (in ML.Cluster.Butina)