Identifier Index

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G

gain (in BitGainsInfo)	GetFPLength() (in FragCatalog)	GetSSSR() (in Chem)
gainsName (in RunDetails)	GetFuncGroup() (in FragCatParams)	GetStereo() (in Bond)
Gaussian (in FeatProfile)	GetGridPointIndex() (in UniformGrid3D_)	GetStereoAtoms() (in Bond)
Gen2DFingerprint() (in Chem.Pharm2D.Generate)	GetGridPointLoc() (in UniformGrid3D_)	GetSubshapeAlignments() (in SubshapeAligner)
Generate (in Chem.Pharm2D)	GetHiddenLayerNodeList() (in Network)	GetSubstructMatch() (in Mol)
GenerateDepictionMatching3DStructure() (in Chem.AllChem)	GetHybridization() (in Atom)	GetSubstructMatches() (in Mol)
GenerateSubshapeShape() (in SubshapeBuilder)	GetId() (in Conformer)	GetSummaries() (in Dbase.Pubmed.Searches)
GenerateSubshapeSkeleton() (in SubshapeBuilder)	GetIdx() (in Atom)	GetSupplementalData() (in ModelPackage)
Generator (in Chem.Pharm2D.LazyGenerator)	GetIdx() (in Bond)	GetSymbol() (in Atom)
GenericPicker (in SimDivFilters.SimilarityPickers)	GetImplicitValence() (in Atom)	GetSymmSSSR() (in Chem.rdmolops)
GenMACCSKeys() (in Chem.MACCSkeys)	GetIncludeBondOrder() (in SigFactory)	GetTableNames() (in DbConnect)
GenVarTable() (in ML.DecTree.ID3)	GetIncludeBondOrder() (in Pharm2DSig)	GetTableNames() (in Dbase.DbInfo)
Geometry	GetIndex() (in Cluster)	getTablesAndViewsSql (in Dbase.DbModule)
GetAcceptor1FeatVects() (in Chem.Features.FeatDirUtils)	GetIndexCombinations() (in Chem.Pharm2D.Utils)	getTablesSql (in Dbase.DbModule)
GetAcceptor1FeatVects() (in Chem.Features.FeatDirUtilsRD)	GetInputData() (in MLDataSet)	GetTanimotoDistMat() (in DataManip.Metric.rdMetricMatrixCalc)
GetAcceptor2FeatVects() (in Chem.Features.FeatDirUtils)	GetInputData() (in MLQuantDataSet)	GetTanimotoSimMat() (in DataManip.Metric.rdMetricMatrixCalc)
GetAcceptor2FeatVects() (in Chem.Features.FeatDirUtilsRD)	GetInputNodeList() (in Network)	GetTerminal() (in TreeNode)
GetAcceptor3FeatVects() (in Chem.Features.FeatDirUtilsRD)	GetInputOrder() (in Composite)	GetTestExamples() (in DecTreeNode)
GetActivityQuantBounds() (in Composite)	GetInputs() (in NetNode)	GetTestExamples() (in KNNModel)
GetAdjacencyMatrix() (in Chem.rdmolops)	GetIsAromatic() (in Atom)	GetTestExamples() (in NaiveBayesClassifier)
GetAlignmentTransform() (in Chem.AllChem)	GetIsAromatic() (in Bond)	GetTolerance() (in FragCatParams)
GetAlignmentTransform() (in Numerics.rdAlignment)	GetIsConjugated() (in Bond)	GetTopN() (in InfoBitRanker)
GetAllChildren() (in RecapHierarchyNode)	GetItemText() (in FastSDMolSupplier)	GetTopologicalTorsionFingerprint() (in Chem.rdMolDescriptors)
GetAllCombinations() (in Chem.Pharm2D.Utils)	GetItemText() (in SDMolSupplier)	GetTopologicalTorsionFingerprintAsIds() (in Chem.AtomPairs.Torsions)
GetAllData() (in Composite)	GetItemText() (in SmilesMolSupplier)	GetTotalNumHs() (in Atom)
GetAllData() (in MLDataSet)	GetItemText() (in TDTMolSupplier)	GetTotalVal() (in DiscreteValueVect)
GetAllData() (in MLQuantDataSet)	getiterator() (in JournalArticleRecord)	GetTotalVal() (in IntSparseIntVect)
GetAllData() (in Forest)	GetLabel() (in SigFactory)	GetTotalVal() (in LongSparseIntVect)
GetAllDescriptorNames() (in ML.Descriptors.CompoundDescriptors)	GetLabel() (in Pharm2DSig)	GetTrainingExamples() (in DecTreeNode)
GetAllNodes() (in Network)	GetLabel() (in TreeNode)	GetTrainingExamples() (in KNNModel)
GetAllPharmacophoreMatches() (in Chem.Pharm3D.EmbedLib)	GetLabels() (in SigFactory)	GetTrainingExamples() (in NaiveBayesClassifier)
GetAromaticFeatVects() (in Chem.Features.FeatDirUtils)	GetLastOutputs() (in Network)	GetTree() (in Forest)
GetAromaticFeatVects() (in Chem.Features.FeatDirUtilsRD)	GetLeaves() (in RecapHierarchyNode)	GetTriangleMatches() (in SubshapeAligner)
GetAtomCoords() (in MolViewer)	GetLength() (in IntSparseIntVect)	GetTriangles() (in Chem.Pharm2D.Utils)
GetAtomCoords() (in MolViewer)	GetLength() (in LongSparseIntVect)	GetType() (in FreeChemicalFeature)
GetAtomFeatInfo() (in Chem.FeatFinderCLI)	GetLevel() (in TreeNode)	GetType() (in MolChemicalFeature)
GetAtomHeavyNeighbors() (in Chem.Pharm3D.EmbedLib)	GetLinks() (in Dbase.Pubmed.Searches)	GetTypeString() (in FragCatParams)
GetAtomicNum() (in Atom)	getLowerBound() (in Pharmacophore)	GetTypeStrings() (in Dbase.DbUtils)
GetAtomicNumber() (in PeriodicTable)	getLowerBound2D() (in Pharmacophore)	getUltimateParents() (in RecapHierarchyNode)
GetAtomicWeight() (in PeriodicTable)	GetLowerFragLength() (in FragCatParams)	getUpperBound() (in Pharmacophore)
GetAtomIds() (in MolChemicalFeature)	GetMass() (in Atom)	getUpperBound2D() (in Pharmacophore)
GetAtomMatch() (in Chem.ChemicalFeatures)	GetMatch() (in FragmentMatcher)	GetUpperFragLength() (in FragCatParams)
GetAtomPairAtomCode() (in Chem.rdMolDescriptors)	GetMatches() (in FragmentMatcher)	GetVal() (in UniformGrid3D_)
GetAtomPairFingerprint() (in Chem.rdMolDescriptors)	GetMaxCount() (in SigFactory)	GetValenceContrib() (in Bond)
GetAtomPairFingerprintAsBitVect() (in Chem.AtomPairs.Pairs)	GetMaxCount() (in Pharm2DSig)	GetValenceList() (in PeriodicTable)
GetAtomPosition() (in Conformer)	GetMaxDist() (in Pharm2DSig)	GetValPoint() (in UniformGrid3D_)
GetAtoms() (in Mol)	GetMetric() (in Cluster)	GetValueType() (in DiscreteValueVect)
GetAtomsMatchingBit() (in Chem.Pharm2D.Matcher)	GetMetricName() (in FingerprinterDetails)	GetVarNames() (in MLDataSet)
GetAtomWithIdx() (in Mol)	GetMinCanvasSize() (in DataStructs.HierarchyVis)	GetVoteDetails() (in Composite)
GetAvailTransforms() (in ML.Data.Transforms)	GetMinCount() (in SigFactory)	GetVoteDetails() (in CompositeServer)
GetBadExamples() (in DecTreeNode)	GetMinCount() (in Pharm2DSig)	GetVoteDetails() (in Forest)
GetBadExamples() (in KNNClassificationModel)	GetMinDist() (in Pharm2DSig)	GetWeights() (in NetNode)
GetBadExamples() (in KNNRegressionModel)	GetModel() (in Composite)	GetWrite2D() (in TDTWriter)
GetBadExamples() (in NaiveBayesClassifier)	GetModel() (in ModelPackage)	GetWriteNames() (in TDTWriter)
GetBeginAtom() (in Bond)	GetMol() (in MolCatalogEntry)	Go() (in ML.ScreenComposite)
GetBeginAtomIdx() (in Bond)	GetMol() (in MolChemicalFeature)	Gobbi_Pharm2D (in Chem.Pharm2D)
GetBin() (in Pharm2DSig)	GetMol() (in EditableMol)	GOWER (in ML.Cluster.Murtagh)
GetBins() (in SigFactory)	GetMoleculeBoundsMatrix() (in Chem.rdDistGeom)	GOWER (in ClusterMethod)
GetBit() (in Generator)	GetMolFeature() (in MolChemicalFeatureFactory)	GraphDescriptors (in Chem)
GetBit() (in Pharm2DSig)	GetMolFrags() (in Chem.rdmolops)	Graphs (in Chem)
GetBit() (in VectCollection)	GetMolsMatchingBit() (in Chem.FragmentCatalog)	greater (in Chem.BuildFragmentCatalog)
GetBit() (in ExplicitBitVect)	GetMoreTerminalPoints() (in Chem.Subshape.BuilderUtils)	greater (in Chem.Crippen)
GetBit() (in SparseBitVect)	GetName() (in Cluster)	greater (in Chem.EState.EState)
GetBitDescription() (in Pharm2DSig)	GetName() (in TreeNode)	greater (in Chem.EState)
GetBitDescription() (in MolCatalog)	GetName() (in KNNModel)	greater (in Chem.Features.FeatDirUtils)
GetBitDescription() (in FragCatalog)	GetName() (in NaiveBayesClassifier)	greater (in Chem.Features.FeatDirUtilsRD)
GetBitDiscrims() (in FragCatalog)	GetNamedData() (in MLDataSet)	greater (in Chem.Fingerprints.ClusterMols)
GetBitEntryId() (in MolCatalog)	GetNamedData() (in MLQuantDataSet)	greater (in Chem.FragmentCatalog)
GetBitEntryId() (in FragCatalog)	GetNeighbors() (in Atom)	greater (in Chem.GraphDescriptors)
GetBitFuncGroupIds() (in FragCatalog)	GetNeighbors() (in KNNModel)	greater (in Chem.Graphs)
GetBitIdx() (in Pharm2DSig)	GetNextId() (in Dbase.StorageUtils)	greater (in Chem.MolSurf)
GetBitInfo() (in Pharm2DSig)	GetNextRDId() (in Dbase.StorageUtils)	greater (in Chem.Pharm2D.Signature)
GetBitOrder() (in FragCatalog)	GetNode() (in Network)	greater (in Chem.Pharm2D.Utils)
GetBits() (in BitEnsemble)	GetNode() (in VLib.NodeLib.DbMolSupply)	greater (in Chem.Pharm3D.EmbedLib)
GetBond() (in FragmentMatcher)	GetNode() (in VLib.NodeLib.DbPickleSupplier)	greater (in Chem.Pharm3D.Pharmacophore)
GetBondBetweenAtoms() (in Mol)	GetNodeList() (in ML.Cluster.ClusterUtils)	greater (in ML.AnalyzeComposite)
GetBondDir() (in Bond)	GetNodesDownToCentroids() (in ML.Cluster.ClusterUtils)	greater (in ML.BuildComposite)
GetBonds() (in Atom)	GetNoImplicit() (in Atom)	greater (in ML.Cluster.Butina)
GetBonds() (in Mol)	GetNonzeroElements() (in IntSparseIntVect)	greater (in ML.Cluster.ClusterUtils)
GetBondType() (in Bond)	GetNonzeroElements() (in LongSparseIntVect)	greater (in ML.Cluster.ClusterVis)
GetBondWithIdx() (in Mol)	GetNotes() (in ModelPackage)	greater (in ML.Cluster.Clusters)
GetCalculator() (in ModelPackage)	GetNOuterElecs() (in PeriodicTable)	greater (in ML.Cluster.Murtagh)
GetCatalogParams() (in FragCatalog)	GetNPossibleVals() (in MLDataSet)	greater (in ML.Cluster.Resemblance)
GetChildren() (in VectCollection)	GetNPts() (in MLDataSet)	greater (in ML.Cluster.Standardize)
GetChildren() (in Cluster)	GetNResults() (in MLDataSet)	greater (in ML.Composite.AdjustComposite)
GetChildren() (in TreeNode)	GetNumAtoms() (in Conformer)	greater (in ML.Composite.BayesComposite)
GetChildren() (in VLibNode)	GetNumAtoms() (in Mol)	greater (in ML.Composite.Composite)
GetChiralTag() (in Atom)	GetNumBins() (in SigFactory)	greater (in ML.Data.MLData)
GetClassificationDetails() (in NaiveBayesClassifier)	GetNumBins() (in Pharm2DSig)	greater (in ML.Data.Quantize)
GetClusters() (in BitClusterer)	GetNumBits() (in BitEnsemble)	greater (in ML.Data.Stats)
GetColumnInfoFromCursor() (in Dbase.DbInfo)	GetNumBits() (in VectCollection)	greater (in ML.Data.Transforms)
GetColumnNames() (in DbFpSupplier)	GetNumBits() (in ExplicitBitVect)	greater (in ML.DecTree.BuildQuantTree)
GetColumnNames() (in DbMolSupplier)	GetNumBits() (in SparseBitVect)	greater (in ML.DecTree.BuildSigTree)
GetColumnNames() (in DbConnect)	GetNumBonds() (in Mol)	greater (in ML.DecTree.CrossValidate)
GetColumnNames() (in Dbase.DbInfo)	GetNumConformers() (in Mol)	greater (in ML.DecTree.Forest)
GetColumnNames() (in DbResultBase)	GetNumDigits() (in TDTWriter)	greater (in ML.DecTree.ID3)
GetColumnNamesAndTypes() (in DbConnect)	GetNumEntries() (in MolCatalog)	greater (in ML.DecTree.PruneTree)
GetColumnNamesAndTypes() (in Dbase.DbInfo)	GetNumEntries() (in FragCatalog)	greater (in ML.DecTree.randomforest)
GetColumnNamesAndTypes() (in DbResultBase)	GetNumExplicitHs() (in Atom)	greater (in ML.EnrichPlot)
GetColumns() (in DbConnect)	GetNumFeatureDefs() (in MolChemicalFeatureFactory)	greater (in ML.GrowComposite)
GetColumns() (in Dbase.DbUtils)	GetNumFeatures() (in FeatMap)	greater (in ML.InfoTheory.BitClusterer)
GetColumnTypes() (in DbResultBase)	GetNumFuncGroups() (in FragCatParams)	greater (in ML.InfoTheory.BitRank)
GetCommandLine() (in ML.BuildComposite)	GetNumHidden() (in Network)	greater (in ML.InfoTheory.entropy)
GetComposites() (in ML.GrowComposite)	GetNumHits() (in Dbase.Pubmed.Searches)	greater (in ML.KNN.CrossValidate)
GetConfidenceInterval() (in ML.Data.Stats)	GetNumImplicitHs() (in Atom)	greater (in ML.MLUtils.VoteImg)
GetConformer() (in Mol)	GetNumMolFeatures() (in MolChemicalFeatureFactory)	greater (in ML.NaiveBayes.ClassificationModel)
GetConformers() (in Mol)	GetNumNodes() (in Network)	greater (in ML.Neural.ActFuncs)
GetCorrMatrix() (in BitCorrMatGenerator)	GetNumOffBits() (in ExplicitBitVect)	greater (in ML.Neural.NetNode)
GetCount() (in Composite)	GetNumOffBits() (in SparseBitVect)	greater (in ML.Neural.Network)
GetCount() (in Forest)	GetNumOnBits() (in ExplicitBitVect)	greater (in ML.Neural.Trainers)
GetCursor() (in DbConnect)	GetNumOnBits() (in SparseBitVect)	greater (in ML.SLT.Risk)
GetData() (in DbConnect)	GetNumPatterns() (in SigFactory)	greater (in ML.ScreenComposite)
GetData() (in Dbase.DbUtils)	GetNumPatterns() (in Pharm2DSig)	greater (in ML.files)
GetData() (in Cluster)	GetNumProductTemplates() (in ChemicalReaction)	greater (in PySVD.SVDPack)
GetData() (in TreeNode)	GetNumReactantTemplates() (in ChemicalReaction)	greater (in PySVD.SVDSimilarity)
GetDataCount() (in DbConnect)	GetNumX() (in UniformGrid3D_)	greater_equal (in Chem.BuildFragmentCatalog)
GetDataSet() (in CompositeRun)	GetNumY() (in UniformGrid3D_)	greater_equal (in Chem.Crippen)
GetDataset() (in ModelPackage)	GetNumZ() (in UniformGrid3D_)	greater_equal (in Chem.EState.EState)
GetDataSetInfo() (in CompositeRun)	GetNVars() (in MLDataSet)	greater_equal (in Chem.EState)
GetDataTuple() (in Composite)	GetOccupancyVect() (in UniformGrid3D_)	greater_equal (in Chem.Features.FeatDirUtils)
GetDataTuple() (in Forest)	GetOffset() (in UniformGrid3D_)	greater_equal (in Chem.Features.FeatDirUtilsRD)
GetDbNames() (in Dbase.DbInfo)	GetOnBits() (in Pharm2DSig)	greater_equal (in Chem.Fingerprints.ClusterMols)
getDbSql (in Dbase.DbModule)	GetOnBits() (in BitVect)	greater_equal (in Chem.FragmentCatalog)
GetDefaultValence() (in PeriodicTable)	GetOnBits() (in SparseBitVect)	greater_equal (in Chem.GraphDescriptors)
GetDegree() (in Atom)	GetOnBits() (in VectCollection)	greater_equal (in Chem.Graphs)
GetDescription() (in MolCatalogEntry)	GetOnBits() (in ExplicitBitVect)	greater_equal (in Chem.MolSurf)
GetDescriptorFuncs() (in MolecularDescriptorCalculator)	GetOnBits() (in SparseBitVect)	greater_equal (in Chem.Pharm2D.Signature)
GetDescriptorNames() (in Composite)	GetOrder() (in MolCatalogEntry)	greater_equal (in Chem.Pharm2D.Utils)
GetDescriptorNames() (in CompositeServer)	GetOrVect() (in VectCollection)	greater_equal (in Chem.Pharm3D.EmbedLib)
GetDescriptorNames() (in CompoundDescriptorCalculator)	GetOtherAtom() (in Bond)	greater_equal (in Chem.Pharm3D.Pharmacophore)
GetDescriptorNames() (in DescriptorCalculator)	GetOtherAtomIdx() (in Bond)	greater_equal (in ML.AnalyzeComposite)
GetDescriptorNames() (in DescriptorServer)	GetOutputNodeList() (in Network)	greater_equal (in ML.BuildComposite)
GetDescriptorNames() (in MolecularDescriptorCalculator)	GetOwningMol() (in Atom)	greater_equal (in ML.Cluster.Butina)
GetDescriptorSummaries() (in MolecularDescriptorCalculator)	GetOwningMol() (in Conformer)	greater_equal (in ML.Cluster.ClusterUtils)
GetDirMatch() (in FeatMapPoint)	GetParent() (in TreeNode)	greater_equal (in ML.Cluster.ClusterVis)
GetDist2() (in FeatMapPoint)	GetParents() (in VLibNode)	greater_equal (in ML.Cluster.Clusters)
GetDistanceMatrix() (in Chem.Fingerprints.ClusterMols)	GetPattern() (in Pharm2DSig)	greater_equal (in ML.Cluster.Murtagh)
GetDistanceMatrix() (in Chem.rdmolops)	GetPatterns() (in SigFactory)	greater_equal (in ML.Cluster.Resemblance)
GetDonor1FeatVects() (in Chem.Features.FeatDirUtils)	GetPeriodicTable() (in Chem)	greater_equal (in ML.Cluster.Standardize)
GetDonor1FeatVects() (in Chem.Features.FeatDirUtilsRD)	GetPoints() (in Cluster)	greater_equal (in ML.Composite.AdjustComposite)
GetDonor2FeatVects() (in Chem.Features.FeatDirUtils)	GetPointsPositions() (in Cluster)	greater_equal (in ML.Composite.BayesComposite)
GetDonor2FeatVects() (in Chem.Features.FeatDirUtilsRD)	GetPos() (in FreeChemicalFeature)	greater_equal (in ML.Composite.Composite)
GetDonor3FeatVects() (in Chem.Features.FeatDirUtils)	GetPos() (in MolChemicalFeature)	greater_equal (in ML.Data.MLData)
GetDonor3FeatVects() (in Chem.Features.FeatDirUtilsRD)	GetPosition() (in Cluster)	greater_equal (in ML.Data.Quantize)
GetElementSymbol() (in PeriodicTable)	GetPossibleScaffolds() (in Chem.Pharm2D.Utils)	greater_equal (in ML.Data.Stats)
GetEndAtom() (in Bond)	GetPrincipleQuantumNumber() (in Chem.EState.EState)	greater_equal (in ML.Data.Transforms)
GetEndAtomIdx() (in Bond)	GetProp() (in Atom)	greater_equal (in ML.DecTree.BuildQuantTree)
GetEntryBitId() (in MolCatalog)	GetProp() (in Bond)	greater_equal (in ML.DecTree.BuildSigTree)
GetEntryBitId() (in FragCatalog)	GetProp() (in Mol)	greater_equal (in ML.DecTree.CrossValidate)
GetEntryDescription() (in MolCatalog)	GetPropNames() (in Mol)	greater_equal (in ML.DecTree.Forest)
GetEntryDescription() (in FragCatalog)	GetPtNames() (in MLDataSet)	greater_equal (in ML.DecTree.ID3)
GetEntryDownIds() (in MolCatalog)	GetPts() (in TopNContainer)	greater_equal (in ML.DecTree.PruneTree)
GetEntryDownIds() (in FragCatalog)	GetQuantBounds() (in Composite)	greater_equal (in ML.DecTree.randomforest)
GetEntryFuncGroupIds() (in FragCatalog)	GetQuantBounds() (in MLDataSet)	greater_equal (in ML.EnrichPlot)
GetEntryOrder() (in FragCatalog)	GetQuantBounds() (in QuantTreeNode)	greater_equal (in ML.GrowComposite)
GetError() (in Composite)	GetRcovalent() (in PeriodicTable)	greater_equal (in ML.InfoTheory.BitClusterer)
GetError() (in Forest)	GetRecords() (in Dbase.Pubmed.Searches)	greater_equal (in ML.InfoTheory.BitRank)
GetEuclideanDistMat() (in DataManip.Metric.rdMetricMatrixCalc)	GetReportlabTable (in Dbase.DbReport)	greater_equal (in ML.InfoTheory.entropy)
GetExamples() (in DecTreeNode)	GetResults() (in MLDataSet)	greater_equal (in ML.KNN.CrossValidate)
GetExamples() (in KNNModel)	GetResults() (in MLQuantDataSet)	greater_equal (in ML.MLUtils.VoteImg)
GetExamples() (in NaiveBayesClassifier)	GetRingInfo() (in Mol)	greater_equal (in ML.NaiveBayes.ClassificationModel)
GetExclusionSMARTS() (in FragmentMatcher)	GetRvdw() (in PeriodicTable)	greater_equal (in ML.Neural.ActFuncs)
GetExplicitValence() (in Atom)	GetScreenImage() (in ML.ScreenComposite)	greater_equal (in ML.Neural.NetNode)
GetExtraPointPos() (in ForceField)	GetSearchIds() (in Dbase.Pubmed.Searches)	greater_equal (in ML.Neural.Network)
GetExtras() (in TopNContainer)	GetSearchURL() (in Dbase.Pubmed.PubmedUtils)	greater_equal (in ML.Neural.Trainers)
GetFactory() (in MolChemicalFeature)	GetSelectedAtoms() (in MolViewer)	greater_equal (in ML.SLT.Risk)
GetFamily() (in FreeChemicalFeature)	GetSelectedAtoms() (in MolViewer)	greater_equal (in ML.ScreenComposite)
GetFamily() (in MolChemicalFeature)	GetShapeShapeDistance() (in Chem.Subshape.SubshapeAligner)	greater_equal (in ML.files)
GetFeatFeatDistMatrix() (in Chem.FeatMaps.FeatMapUtils)	GetShortestPathsOnly() (in SigFactory)	greater_equal (in PySVD.SVDPack)
GetFeatFeatScore() (in FeatMap)	GetShortestPathsOnly() (in Pharm2DSig)	greater_equal (in PySVD.SVDSimilarity)
GetFeature() (in FeatMap)	GetSignature() (in SigFactory)	grid (in ShapeWithSkeleton)
getFeature() (in Pharmacophore)	GetSingleFingerprint() (in SimilarityScreener)	gridDims (in SubshapeBuilder)
GetFeatures() (in FeatMap)	GetSize() (in Pharm2DSig)	gridSpacing (in SubshapeBuilder)
getFeatures() (in Pharmacophore)	GetSize() (in UniformGrid3D_)	Grow() (in Composite)
GetFingerprints() (in Chem.Fingerprints.MolSimilarity)	GetSMARTS() (in FragmentMatcher)	Grow() (in Forest)
GetFormalCharge() (in Atom)	GetSmarts() (in Atom)	GrowComposite (in ML)
GetFormalCharge() (in Chem.rdmolops)	GetSmarts() (in Bond)	GrowIt() (in ML.GrowComposite)
GetFPForMol() (in FragFPGenerator)	GetSmartsMatchCDXML() (in Chem)
GetFPLength() (in MolCatalog)	GetSpacing() (in UniformGrid3D_)