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 _ ]

I

i (in VLib.NodeLib.demo)	info() (in logger)	InsertColumnData() (in DbConnect)
I (in re)	InfoBitRanker (in ML.InfoTheory.rdInfoTheory)	InsertData() (in DbConnect)
id (in BitGainsInfo)	InfoGain() (in ML.InfoTheory.rdInfoTheory)	INTERSECT (in SubshapeCombineOperations)
ID3 (in ML.DecTree)	InfoTheory (in ML)	IntSparseIntVect (in DataStructs.cDataStructs)
ID3() (in ML.DecTree.ID3)	InfoType (in ML.InfoTheory.rdInfoTheory)	InvertChirality() (in Atom)
ID3Boot() (in ML.DecTree.ID3)	Init() (in Chem.Draw.DrawUtils)	io (in VLib.NodeLib.demo)
idx1 (in Chem.BuildFragmentCatalog)	init() (in FastSDMolSupplier)	IONIC (in BondType)
idx1 (in Chem.Fingerprints.ClusterMols)	Init() (in FragmentMatcher)	Ipc() (in Chem.GraphDescriptors)
idx1 (in Chem.Fingerprints.FingerprintMols)	Init() (in Pharm2DSig)	Is3D() (in Conformer)
idx1 (in Chem.Fingerprints.MolSimilarity)	Init() (in ModelPackage)	IsAtomInRingOfSize() (in RingInfo)
idx2 (in Chem.BuildFragmentCatalog)	InitFromDaylightString() (in DataStructs)	IsBondInRingOfSize() (in RingInfo)
idx2 (in Chem.Fingerprints.ClusterMols)	initFromFeat() (in FeatMapPoint)	IsInRing() (in Atom)
idx2 (in Chem.Fingerprints.FingerprintMols)	initFromFile() (in ExplicitPharmacophore)	IsInRing() (in Bond)
idx2 (in Chem.Fingerprints.MolSimilarity)	initFromLines() (in ExplicitPharmacophore)	IsInRingSize() (in Atom)
Ignore (in FeatDirScoreMode)	InitFromSequence() (in pySparseIntVect)	IsInRingSize() (in Bond)
IGNORECASE (in re)	initFromString() (in ExplicitPharmacophore)	isNaN() (in Chem.Pharm3D.EmbedLib)
includeAtomNumbers (in MolDrawing)	Initialize() (in ForceField)	isPresent() (in Logger.Logger)
IndexToRDId() (in Dbase.StorageUtils)	InitializePyMol() (in MolViewer)	IsTerminal() (in Cluster)
inFileName (in RunDetails)	InitRandomNumbers() (in ML.Data.DataUtils)
INFO (in RDLogger)	Insert() (in TopNContainer)