Trees
Indices
Help
RDKit
[
hide private
]
[
frames
] |
no frames
]
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
_
]
P
Packager
(in
rdkit.ML.ModelPackage
)
PEOE_VSA_()
(in
rdkit.Chem.MolSurf
)
ProcessGainsData()
(in
rdkit.Chem.BuildFragmentCatalog
)
PackageToXml()
(in
rdkit.ML.ModelPackage.PackageUtils
)
periodicData
(in
rdkit.Chem.PeriodicTable'
)
ProcessGainsFile()
(in
rdkit.Chem.FragmentCatalog
)
PackageUtils
(in
rdkit.ML.ModelPackage
)
periodicTable
(in
rdkit.Chem.GraphDescriptors
)
ProcessIt()
(in
rdkit.ML.AnalyzeComposite
)
PackPoint()
(in
SimilarityCalculator
)
PeriodicTable
(in
rdkit.Chem.rdchem
)
ProcessMol()
(in
rdkit.Chem.MolDb.Loader
)
Pairs
(in
rdkit.Chem.AtomPairs
)
PeriodicTable'
(in
rdkit.Chem
)
ProcessSimpleList()
(in
CompoundDescriptorCalculator
)
params
(in
FeatMap
)
permutation()
(in
rdkit.ML.Data.DataUtils
)
PROTRUDE
(in
SubshapeDistanceMetric
)
parents
(in
RecapHierarchyNode
)
Pharm2D
(in
rdkit.Chem
)
ProtrudeDistance()
(in
rdkit.Geometry.rdGeometry
)
Parse()
(in
FeatMapParser
)
Pharm2DSig
(in
rdkit.Chem.Pharm2D.Signature
)
PruneChild()
(in
TreeNode
)
ParseArgs()
(in
rdkit.Chem.BuildFragmentCatalog
)
Pharm3D
(in
rdkit.Chem
)
PruneMatchesUsingDirection()
(in
SubshapeAligner
)
ParseArgs()
(in
rdkit.Chem.Fingerprints.FingerprintMols
)
Pharmacophore
(in
rdkit.Chem.Pharm3D
)
PruneMatchesUsingFeatures()
(in
SubshapeAligner
)
ParseArgs()
(in
rdkit.ML.BuildComposite
)
Pharmacophore
(in
rdkit.Chem.Pharm3D.Pharmacophore
)
PruneMatchesUsingShape()
(in
SubshapeAligner
)
ParseArgs()
(in
rdkit.ML.GrowComposite
)
pi
(in
rdkit.Chem.Features.FeatDirUtils
)
PruneTree
(in
rdkit.ML.DecTree
)
ParseArgs()
(in
rdkit.ML.ScreenComposite
)
pi
(in
rdkit.ML.Descriptors.Parser
)
PruneTree()
(in
rdkit.ML.DecTree.PruneTree
)
ParseChemicals()
(in
JournalArticleRecord
)
pi
(in
rdkit.PySVD.SVDPack
)
ps
(in
rdkit.Chem.BRICS
)
ParseFeatPointBlock()
(in
FeatMapParser
)
pi
(in
rdkit.PySVD.SVDSimilarity
)
Pubmed
(in
rdkit.Dbase
)
ParseKeywords()
(in
JournalArticleRecord
)
Pick()
(in
HierarchicalClusterPicker
)
PubmedUtils
(in
rdkit.Dbase.Pubmed
)
ParseParamBlock()
(in
FeatMapParser
)
Pick()
(in
MaxMinPicker
)
pyDiceSimilarity()
(in
rdkit.DataStructs.SparseIntVect
)
parser
(in
rdkit.Chem.Features.ShowFeats
)
Pickle()
(in
Composite
)
PyInfoEntropy()
(in
rdkit.ML.InfoTheory.entropy
)
Parser
(in
rdkit.ML.Descriptors
)
Pickle()
(in
Forest
)
PyInfoEntropy()
(in
rdkit.ML.InfoTheory.entropy
)
PEOE_VSA1()
(in
rdkit.Chem.MolSurf
)
Pickle()
(in
TreeNode
)
PyInfoGain()
(in
rdkit.ML.InfoTheory.entropy
)
PEOE_VSA10()
(in
rdkit.Chem.MolSurf
)
placeHolder
(in
rdkit.Dbase.DbModule
)
pyLabuteASA()
(in
rdkit.Chem.MolSurf
)
PEOE_VSA11()
(in
rdkit.Chem.MolSurf
)
Point2D
(in
rdkit.Geometry.rdGeometry
)
PyMol
(in
rdkit.Chem
)
PEOE_VSA12()
(in
rdkit.Chem.MolSurf
)
Point3D
(in
rdkit.Geometry.rdGeometry
)
pyMolLogP()
(in
rdkit.Chem.Crippen
)
PEOE_VSA13()
(in
rdkit.Chem.MolSurf
)
PointND
(in
rdkit.Geometry.rdGeometry
)
pyMolMR()
(in
rdkit.Chem.Crippen
)
PEOE_VSA14()
(in
rdkit.Chem.MolSurf
)
power
(in
rdkit.Chem.Features.FeatDirUtils
)
pyMolWt()
(in
rdkit.Chem.Descriptors
)
PEOE_VSA2()
(in
rdkit.Chem.MolSurf
)
power
(in
rdkit.PySVD.SVDPack
)
pyScorePair()
(in
rdkit.Chem.AtomPairs.Pairs
)
PEOE_VSA3()
(in
rdkit.Chem.MolSurf
)
power
(in
rdkit.PySVD.SVDSimilarity
)
pyScorePath()
(in
rdkit.Chem.AtomPairs.Torsions
)
PEOE_VSA4()
(in
rdkit.Chem.MolSurf
)
PredictExample()
(in
KNNRegressionModel
)
pySparseIntVect
(in
rdkit.DataStructs.SparseIntVect
)
PEOE_VSA5()
(in
rdkit.Chem.MolSurf
)
PrepareDataFromDetails()
(in
rdkit.ML.ScreenComposite
)
PySVD
(in rdkit)
PEOE_VSA6()
(in
rdkit.Chem.MolSurf
)
PrincipalComponents()
(in
rdkit.ML.Data.Stats
)
pythonExe
(in
RDConfig
)
PEOE_VSA7()
(in
rdkit.Chem.MolSurf
)
Print()
(in
Cluster
)
pythonTestCommand
(in
RDConfig
)
PEOE_VSA8()
(in
rdkit.Chem.MolSurf
)
Print()
(in
TreeNode
)
PEOE_VSA9()
(in
rdkit.Chem.MolSurf
)
ProcessCompoundList()
(in
CompoundDescriptorCalculator
)
Trees
Indices
Help
RDKit
Generated by Epydoc 3.0.1 on Fri Apr 3 06:05:31 2009
http://epydoc.sourceforge.net