SDF Reader

Input Ports

This node has no input ports

Output Ports

Table with the read molecules

Table with illegal SDF records

Popular Predecessors

• SDF Writer15 %
• Table Row to Variable Loop Start14 %
• Path to String (Variable)6 %
• Table Row to Variable4 %
• Table Column to Variable4 %
• Show all 90 recommendations

Popular Successors

• RDKit From Molecule8 %
• Joiner5 %
• Column Filter3 %
• Row Filter3 %
• Molecule Type Cast2 %
• RDKit Canon SMILES2 %
• 3D Coordinates2 %
• Table to PDF (legacy)2 %
• RDKit Descriptor Calculation2 %
• SDF Extractor2 %
• MolConverter2 %
• SDF Writer2 %
• Concatenate2 %
• SDF Stripper1 %
• Reference Row Filter1 %
• Column Rename1 %
• Generate 3D Coordinates1 %
• Molecule to CDK1 %
• GroupBy< 1 %
• Fingerprints< 1 %
• RDKit Molecule Substructure Filter< 1 %
• OpenBabel< 1 %
• RDKit Fingerprint< 1 %
• Duplicate Row Filter< 1 %
• RDKit To Molecule< 1 %
• String Manipulation< 1 %
• Constant Value Column< 1 %
• Row Splitter< 1 %
• Molecule-to-MAE< 1 %
• Sorter< 1 %
• LigPrep< 1 %
• RDKit Substructure Filter< 1 %
• Cell Splitter< 1 %
• RDKit Salt Stripper< 1 %
• RDKit Two Component Reaction< 1 %
• Rule-based Row Filter< 1 %
• RowID< 1 %
• Loop End< 1 %
• RDKit Diversity Picker< 1 %
• Math Formula< 1 %
• Molecular Properties< 1 %
• Column Splitter< 1 %
• MarvinSpace< 1 %
• Table View (JavaScript)< 1 %
• Molecule Converter (Naomi)< 1 %
• Excel Writer< 1 %
• String To Number< 1 %
• CSV Writer< 1 %
• 3D Coordinates Generator< 1 %
• Reference Row Splitter< 1 %
• RDKit Functional Group Filter< 1 %
• Compute LeadIT Docking< 1 %
• Validation and Normalisation< 1 %
• RDKit Molecule Catalog Filter< 1 %
• Canonical SMILES< 1 %
• MCS Scaffold Finder< 1 %
• Column Combiner< 1 %
• Value Counter< 1 %
• RDKit To InChI< 1 %
• Rule-based Row Splitter< 1 %
• Lipinski's Rule-of-Five< 1 %
• Substructure Matcher< 1 %
• SD-to-Smiles< 1 %
• ChEMBLdb Connector Input< 1 %
• logD< 1 %
• Advanced MolConverter< 1 %
• Joiner< 1 %
• Counter Generation< 1 %
• Compute FlexS Alignments< 1 %
• Counting Loop Start< 1 %
• Molecule Filter (Naomi)< 1 %
• Column Renamer< 1 %
• Docking (FlexX)< 1 %
• Automated Matched Pairs< 1 %
• Normalizer< 1 %
• Rule Engine< 1 %
• RDKit Structure Normalizer< 1 %
• Similarity Matrix (from Molecules)< 1 %
• Variable to Table Column< 1 %
• Row Sampling< 1 %
• Renderer to Image< 1 %
• Table to PDF< 1 %
• RDKit Find Murcko Scaffolds< 1 %
• RDKit R-Group Decomposition< 1 %
• Parameterized Database Query< 1 %
• Loop End (2 ports)< 1 %
• Chunk Loop Start< 1 %
• Linear Regression Learner< 1 %
• MoleculeTransform< 1 %
• Unpivot< 1 %
• Major Microspecies< 1 %
• Python Script< 1 %
• Assess Affinity with Hyde in SeeSAR< 1 %
• PMI Calculation< 1 %
• Plane of Best Fit Calculator< 1 %
• Table Row To Variable Loop Start< 1 %
• Linear Correlation< 1 %
• RDKit R-Group Decomposition (deprecated)< 1 %
• RDKit Substructure Counter< 1 %
• Data to Report< 1 %
• Standardizer< 1 %
• Virtual Screening Metrics< 1 %
• Group Loop Start< 1 %
• Regression Predictor< 1 %
• Pivot< 1 %
• String Replacer< 1 %
• Dragon 7.0 Descriptors< 1 %
• Substructure Search< 1 %
• RDKit Add Conformers< 1 %
• Column Appender< 1 %
• Substructure Match Counter< 1 %
• pKa< 1 %
• Nominal Value Row Splitter< 1 %
• Smiles Directory Writer< 1 %
• Java Snippet Row Splitter< 1 %
• CDK to Molecule< 1 %
• RDKit One Component Reaction< 1 %
• RDKit Molecule to SVG< 1 %
• Filter Molecules with Naomi< 1 %
• Component Separator< 1 %
• Loop End< 1 %
• Category to Number< 1 %
• Column Merger< 1 %
• Numeric Row Splitter< 1 %
• Mol2 Writer< 1 %
• Fingerprint Bayesian Predictor< 1 %
• RDKit Remove Hs< 1 %
• SD Format Checker< 1 %
• ECFP/FCFP< 1 %
• Table Writer< 1 %
• Table Manipulator< 1 %
• Glide Ligand Docking< 1 %
• QikProp< 1 %
• Speedy SMILES Enumerate Stereoisomers< 1 %
• Ligands and Proteins Viewer< 1 %
• Upload (legacy)< 1 %
• Java Snippet< 1 %
• Round Double< 1 %
• Component Output< 1 %
• Random Number Assigner< 1 %
• Value Selection (legacy)< 1 %
• SMARTCyp 2.4.2< 1 %
• Mass Calculator< 1 %
• RDKit Open 3D Alignment< 1 %
• RDKit Optimize Geometry< 1 %
• RDKit SDF Difference Checker< 1 %
• SDF Writer< 1 %
• Excel Writer (XLS)< 1 %
• RDKit Molecule Fragmenter< 1 %
• PMI Triangle Scatter Plot< 1 %
• Library Preparation< 1 %
• Reaxys Reactions< 1 %
• Feature Remover< 1 %
• Indigo Fingerprint< 1 %
• MMP Molecule Fragment (3rd Gen)< 1 %
• Chemical Fingerprint< 1 %
• Fragmenter< 1 %
• LibraryMCS< 1 %
• Database Writer< 1 %
• Hierarchical Clustering< 1 %
• Set Operator< 1 %
• Cache< 1 %
• SDF Inserter< 1 %
• Generic Web Service Client< 1 %
• External Tool< 1 %
• XLS Writer< 1 %
• Java Snippet Row Filter< 1 %
• Structure Converter< 1 %
• Connectivity< 1 %
• 2D Coordinates< 1 %
• RDKit Add Hs< 1 %
• RDKit Chemical Transformation< 1 %
• RDKit Kekulizer< 1 %
• RDKit RMSD Filter< 1 %
• pyflare< 1 %
• Principal Moment of Intertia (PMI)-Derived Properties< 1 %
• CASE Switch Data (End)< 1 %
• Parameterized DB Query Reader< 1 %
• Ligands Viewer< 1 %
• Variable Timed Loop End< 1 %
• Variable to Table Column< 1 %
• Column Expressions< 1 %
• Generate FTrees< 1 %
• CIR< 1 %
• Space Query Generator (FTrees)< 1 %
• Molecule Properties< 1 %
• Standardizer< 1 %
• Molecule Transformation (beta)< 1 %
• Canvas Molecular Descriptors< 1 %
• MMP Molecule Fragment (RDKit)< 1 %
• 3D Alignment< 1 %
• Bi Reactor< 1 %
• Cell Replacer< 1 %
• Cell Splitter By Position< 1 %
• Column Renamer (Dictionary)< 1 %
• Reference Column Filter< 1 %
• Nominal Value Row Filter< 1 %
• Partitioning< 1 %
• Number To String (PMML)< 1 %
• Rank< 1 %
• Merge Variables< 1 %
• Molfile Writer< 1 %
• Parallel Chunk Start< 1 %
• MoSS MCSS Molecule Similarity< 1 %
• External SSH Tool< 1 %
• Standardize< 1 %
• 3D RMSD< 1 %
• RDKit Generate Coords< 1 %
• RDKit Aromatizer< 1 %
• RDKit Interactive Table< 1 %
• RDKit From IUPAC< 1 %
• RDKit MCS< 1 %
• SeeSAR Project Generator< 1 %
• AutoDock Vina< 1 %
• SMARTSViewer< 1 %
• Column Rename (Regex)< 1 %
• Missing Value Column Filter< 1 %
• Reaction Space Generator< 1 %
• MOL to SMARTS< 1 %
• MOE Descriptors< 1 %
• Hydrogen Adder< 1 %
• Molecule Properties< 1 %
• Murcko Scaffold< 1 %
• Valence Checker< 1 %
• Canvas Fingerprint Generation< 1 %
• KNIME-Maestro Connector< 1 %
• Align to Inertial Principal Axes< 1 %
• MolSearch< 1 %
• Naming< 1 %
• MarvinView< 1 %
• ChemSpider< 1 %
• 2D/3D Scatterplot< 1 %
• Table Row to Variable< 1 %
• Java Edit Variable< 1 %
• Column List Loop Start< 1 %
• Numeric Scorer< 1 %
• Column Aggregator< 1 %
• String Manipulation (Variable)< 1 %
• Similarity Search< 1 %
• Table to HTML< 1 %
• MoSS< 1 %
• Histogram Chart (JFreeChart)< 1 %
• VEGA 1.1.1 Models< 1 %
• Validation< 1 %
• 3D D-Similarity< 1 %
• XLogP< 1 %
• RDKit Molecule Extractor< 1 %
• Predictor< 1 %
• Patent< 1 %
• Ligand-based Pharmacophore Creator< 1 %
• Chemical File Writer< 1 %
• Ligand Preparation< 1 %
• Generate Smarts< 1 %
• Structure Filter< 1 %
• Validation and Normalisation (V2)< 1 %
• Induced Fit Docking< 1 %
• Flare Docking< 1 %
• Table Row to Variable Loop Start< 1 %
• DeepAutoQSAR Predict< 1 %
• Chemical Space Searcher (FTrees)< 1 %
• Reaction Product Enumerator< 1 %
• InChI< 1 %
• Spark Database Search< 1 %
• Spark Fragment Selector< 1 %
• InChi< 1 %
• Weight Splitter< 1 %
• Knime To SDF Port< 1 %
• Pharmacophore/Molecule Clustering< 1 %
• Fingerprint Clustering< 1 %
• Maestro Molecular Properties< 1 %
• Substructure Search< 1 %
• LigPrep (deprecated)< 1 %
• Lookup and Add Columns< 1 %
• Generate Unique Smiles< 1 %
• Speedy SMILES De-salt< 1 %
• Outlier Removal< 1 %
• Chemical Terms< 1 %
• logP< 1 %
• MCS< 1 %
• Reactor< 1 %
• Structure Checker< 1 %
• Molecule Difference Checker< 1 %
• Create File Name (legacy)< 1 %
• Loop End (Column Append)< 1 %
• Regression Predictor< 1 %
• Create Bit Vector< 1 %
• Column Auto Type Cast< 1 %
• Number To String< 1 %
• Column Resorter< 1 %
• Cross Joiner< 1 %
• Column Filter< 1 %
• Reference Column Splitter< 1 %
• Column Filter (PMML)< 1 %
• Missing Value< 1 %
• Shuffle< 1 %
• Rule-based Row Filter (Dictionary)< 1 %
• Interactive Table (legacy)< 1 %
• Distance Matrix Calculate< 1 %
• PMML Predictor< 1 %
• Math Formula (Multi Column)< 1 %
• Java Snippet (simple)< 1 %
• Java IF (Table)< 1 %
• Column Filter (legacy)< 1 %
• Table Editor (JavaScript)< 1 %
• Table to HTML String< 1 %
• Orion Model Predictor for Effiris Branch< 1 %
• Sarah Model Maker< 1 %
• Fingerprint Similarity< 1 %
• RDKit Calculate Charges< 1 %
• RDKit From InChI< 1 %
• PaDEL-Descriptor< 1 %
• Molecule to SMILES< 1 %
• Fingerprint Calculator< 1 %
• MolConvertTo3D< 1 %
• Bi Reactor (By Input)< 1 %
• Metabolizer< 1 %
• Aqueous Solubility< 1 %
• Desirability Ranking< 1 %
• X-Partitioner< 1 %
• Decision Tree Predictor< 1 %
• Number to String< 1 %
• String to Number< 1 %
• Rule Engine< 1 %
• Save Workflow< 1 %
• PPilot Connector< 1 %
• Python Script (2⇒1)< 1 %
• MAE-to-Smiles< 1 %
• Bemis-Murcko< 1 %
• Split Into Fragments< 1 %
• Table Row to Variable< 1 %
• DB Table Creator< 1 %
• LIBSVMPredictor< 1 %
• Python Script (legacy)< 1 %
• Path to String< 1 %
• HiLite Row Splitter< 1 %
• Run Maestro Command< 1 %
• Phase DB Creation< 1 %
• Fingerprint From String< 1 %
• MDS Projection (DistMatrix)< 1 %
• ComplianceChecker< 1 %
• DeepAutoQSAR Build< 1 %
• Tautomer Generator< 1 %
• Similarity Calculator (FTrees)< 1 %
• Write MDB< 1 %
• Component Combiner< 1 %
• Hydrogen Remover< 1 %
• Molecule to Indigo (deprecated)< 1 %
• Standard Properties< 1 %
• Shape Screening< 1 %
• Python Snippet< 1 %
• Python Snippet< 1 %
• Elemental Analysis< 1 %
• JChem Oracle Cartridge< 1 %
• Ligands Viewer< 1 %
• Activity Cliffs Viewer< 1 %
• File Reader< 1 %
• Cluster Assigner< 1 %
• Hierarchical Clustering (DistMatrix)< 1 %
• Random Forest Predictor< 1 %
• Cell Splitter< 1 %
• Column Appender< 1 %
• Low Variance Filter< 1 %
• Normalizer (Apply)< 1 %
• Create Temp Dir (legacy)< 1 %
• Matrix Distance< 1 %
• HeatMap (JFreeChart)< 1 %
• PaDEL 2D (beta)< 1 %
• 3D Viewer< 1 %
• Duplicate Remover< 1 %
• MMP Molecule Multi-cut Fragment (RDKit)< 1 %
• Distance (3-D)< 1 %
• Filter Apply Row Splitter< 1 %
• GET Request< 1 %
• Predict< 1 %
• MAE-to-SD< 1 %
• Protein Preparation Wizard< 1 %
• Reaction Based Enumeration< 1 %
• Path to String (Variable)< 1 %
• Virtual Screening< 1 %
• Compute LeadIT Docking< 1 %
• Fingerprint< 1 %
• Most Similar Molecule(s)< 1 %
• FieldTemplater< 1 %
• Dearomatizer< 1 %
• Generate 2D Coordinates< 1 %
• Reaction Automapper< 1 %
• R-Group Decomposer< 1 %
• Chiralator< 1 %
• Glide Ligand Docking< 1 %
• Stereoizer< 1 %
• Loop End (Upto 6 ports)< 1 %
• Uniquify IDs< 1 %
• Python Plot< 1 %
• Get MolName And Comment< 1 %
• Maccs Fingerprint< 1 %
• Pharmacophore from molecule< 1 %
• Pharmacophore (local files)< 1 %
• De Novo Structure Generator with Scheme Awareness< 1 %
• Fingerprint Similarity< 1 %
• Table to Image< 1 %
• Simple Regression Tree Predictor< 1 %
• Subset Matcher< 1 %
• Regex Split< 1 %
• Statistics< 1 %
• Scatter Plot (JFreeChart)< 1 %
• Excel Writer (XLS)< 1 %
• SimpleKMeans (3.7)< 1 %
• Python Script (1⇒1)< 1 %
• R Snippet< 1 %
• Dragon 7.0 Fingerprints< 1 %
• SMARTS Query< 1 %
• RDKit Adjust Query Properties< 1 %
• RDKit Count-Based Fingerprint< 1 %
• Interactive BioSolveIT Viewer< 1 %
• Wash< 1 %
• Align Binding Sites< 1 %
• Extract Atom/bond Properties< 1 %
• Run Maestro< 1 %
• Force Field Conformer Energies< 1 %
• IF Switch (Flow Variable Value)< 1 %
• Timed Loop End (1 port)< 1 %
• MMP Show Cuttable Bonds (RDKit)< 1 %
• Benchmark Start< 1 %
• MarvinTable< 1 %
• Uni Reactor< 1 %
• Pareto Ranking< 1 %
• K Nearest Neighbor< 1 %
• Auto-Binner< 1 %
• Interactive HiLite Collector< 1 %
• Ungroup< 1 %
• Binary Scorer< 1 %
• Affinity Calculator (HYDE)< 1 %
• SeeSAR Project Generator< 1 %
• Merge< 1 %
• Load SD-Files (SDF)< 1 %
• Top k Row Filter< 1 %
• Rule Engine Variable< 1 %
• Capture Workflow Start< 1 %
• Strings to Document< 1 %
• String to Path (Variable)< 1 %
• Container Input (Table)< 1 %
• Compute FTrees Alignments (3D)< 1 %
• Interactive SeeSAR Viewer< 1 %
• CATS Descriptor< 1 %
• Duplicate Filter< 1 %
• Forge Align< 1 %
• Forge Build Field QSAR< 1 %
• Generate Spark Database< 1 %
• Filter< 1 %
• Reaction Splitter< 1 %
• Diversity Picker< 1 %
• MolUnique< 1 %
• Hierarchical Clustering< 1 %
• Extract Properties< 1 %
• Run PyMOL< 1 %
• Speedy SMILES Element Count (C, N, O)< 1 %
• MMP Calculate Maximum Cuts (RDKit)< 1 %
• MMP Molecule Filter< 1 %
• MMP Molecule Multi-cut Fragment (3rd Gen)< 1 %
• PDB Saver< 1 %
• PubChem Compounds< 1 %
• JChem Update< 1 %
• Markush Viewer< 1 %
• MolFragmenter< 1 %
• MolSimilarity< 1 %
• Screen3D< 1 %
• Sphere Exclusion< 1 %
• DbModelEval< 1 %
• Kendall Tau< 1 %
• SyGMa Metabolites< 1 %
• CheS-Mapper< 1 %
• Free-Wilson Matched Pairs< 1 %
• Zip Files (legacy)< 1 %
• CSV Writer< 1 %
• Table Writer< 1 %
• Backward Feature Elimination Filter< 1 %
• Hierarchical Cluster Assigner (local)< 1 %
• Decision Tree Learner< 1 %
• PCA Compute< 1 %
• Column Name Extractor< 1 %
• One to Many< 1 %
• Correlation Filter< 1 %
• Double to Integer< 1 %
• String Replace (Dictionary)< 1 %
• Table Transposer< 1 %
• Timer Info< 1 %
• Histogram (legacy)< 1 %
• Scatter Matrix (legacy)< 1 %
• DL4J Feedforward Learner (Classification) (legacy)< 1 %
• DL4J Feedforward Predictor (Classification) (legacy)< 1 %
• Table Indexer< 1 %
• Java Edit Variable (simple)< 1 %
• Strings To Document< 1 %
• Column Selection (legacy)< 1 %
• Image Writer< 1 %
• Python Predictor< 1 %
• Python Script (1⇒1)< 1 %
• Inchi< 1 %
• Fame< 1 %
• Fingerprinter< 1 %
• Hydrogen Manipulator< 1 %
• ClusteringKohonen< 1 %
• Tautomer Generator (Naomi)< 1 %
• Chemspace Search< 1 %
• Forge Score k Nearest Neighbor (kNN)< 1 %
• Organic Splitter< 1 %
• Maximum Common Substructure Search< 1 %
• Table Row To Variable Run-for-time Loop Start< 1 %
• MMP Molecule Filter (RDKit)< 1 %
• Dose Response (R)< 1 %
• Open in Python (deprecated)< 1 %
• CNMR Prediction< 1 %
• Mass Scalar Descriptor< 1 %
• R-group Composition< 1 %
• Stereoisomers< 1 %
• Clean Data< 1 %
• Extract pharmacophore points< 1 %
• Similar fragments< 1 %
• Extract URI Info< 1 %
• URL to File Path< 1 %
• Try (Variable Ports)< 1 %
• Variable to Table Column< 1 %
• Table Column to Variable< 1 %
• Expand Bit Vector< 1 %
• Domain Calculator< 1 %
• Extract Table Dimension< 1 %
• Oracle Connector< 1 %
• TIBCO File Writer< 1 %
• Heatmap (JavaScript)< 1 %
• Moving Aggregator< 1 %
• String to XML< 1 %
• Lhasa Type Caster< 1 %
• Atom Signatures< 1 %
• 3D D-Moments< 1 %
• CmdwInput< 1 %
• ChEBI Searcher< 1 %
• Molecule Aligner (FlexS)< 1 %
• Flare Align< 1 %
• Activity Profiling< 1 %
• Call Remote Workflow (Row Based)< 1 %
• Glide Sort Results< 1 %
• Ligfilter< 1 %
• Set MAE Properties< 1 %
• Templated Conformer Generation (RDKit)< 1 %
• Speedy SMILES Possible Stereoisomer Count< 1 %
• Notched Boxplot (JFreechart)< 1 %
• Structures PDB Mapper< 1 %
• Catch Errors (Data Ports)< 1 %
• Database Delete< 1 %
• Variable Condition Loop End< 1 %
• Random Forest Learner< 1 %
• String Manipulation (Multi Column)< 1 %
• Parallel Chunk End< 1 %
• Date Field Extractor (legacy)< 1 %
• EffirisPredictor< 1 %
• Convert Molecules with Naomi< 1 %
• Assess Affinity with Hyde in SeeSAR< 1 %
• Interactive BioSolveIT Table< 1 %
• ActMolecule from Molecule< 1 %
• Descriptor< 1 %
• Chemical Space Merger< 1 %
• Closest Neighbor(s)< 1 %
• Molecule Filter< 1 %
• Pharmacophore Search< 1 %
• Scaffold Classification Approach< 1 %
• Substructure Search< 1 %
• Activity Miner< 1 %
• Torch/Forge Molecule Viewer< 1 %
• XedMin< 1 %
• Create Property< 1 %
• Create Record< 1 %
• Combinatorial Reaction Enumeration (beta)< 1 %
• Isomer Enumerator< 1 %
• Reaction Builder< 1 %
• ICon< 1 %
• AutoDock 4< 1 %
• LDB Writer< 1 %
• CORINA< 1 %
• MolAPFSuperimpose< 1 %
• MolCalcProp< 1 %
• MolIcmDock< 1 %
• Molecule Properties< 1 %
• R-Group Decomposer Extended< 1 %
• Epik Classic< 1 %
• Generate Pairwise Matrix< 1 %
• Glide Ensemble Docking< 1 %
• Glide Merge< 1 %
• Ionizer< 1 %
• Molecule Writer (from MAE)< 1 %
• RMSD< 1 %
• Set Molecule Title< 1 %
• Table Viewer< 1 %
• Speedy SMILES Heavy Atom Count (HAC)< 1 %
• Speedy SMILES Explicit Chirality Splitter< 1 %
• Speedy SMILES Remove Multicomponent molecules Splitter< 1 %
• IF Switch (Flow Variable Value)< 1 %
• MMP Molecule Splitter< 1 %
• NameLookup< 1 %
• IC Synth< 1 %
• PubChem Substances< 1 %
• Fuse Fragments< 1 %
• JChem Search< 1 %
• PubChem Search< 1 %
• R-group Decomposition< 1 %
• Structural Frameworks< 1 %
• Tri Reactor< 1 %
• Get Structure< 1 %
• Molecule Properties< 1 %
• Multi Scoring< 1 %
• Pains< 1 %
• Pharmacophores Viewer< 1 %
• Pharmacophore< 1 %
• Ligands Overview Retriever< 1 %
• Reaction Vector Structure Generator< 1 %
• Similarity Viewer< 1 %
• File Meta Info< 1 %
• URL to File Path (Variable)< 1 %
• Extract Variables (Data)< 1 %
• Table Column to Variable< 1 %
• Image Writer (Table Column)< 1 %
• CSV Reader< 1 %
• Variable Condition Loop End< 1 %
• Generic Loop Start< 1 %
• Naive Bayes Predictor< 1 %
• RProp MLP Learner< 1 %
• PCA Apply< 1 %
• SVM Learner< 1 %
• Gradient Boosted Trees Learner< 1 %
• Tree Ensemble Predictor (Regression)< 1 %
• Perl Scripting< 1 %
• Concatenate (Optional in)< 1 %
• Case Converter< 1 %
• Number to Category (Apply)< 1 %
• Many to One< 1 %
• Table Validator (Reference)< 1 %
• Filter Apply< 1 %
• Missing Value (Apply)< 1 %
• Independent groups t-test< 1 %
• Empty Table Switch< 1 %
• End IF< 1 %
• IF Switch< 1 %
• Extract Table Spec< 1 %
• Interactive Histogram (legacy)< 1 %
• Box Plot (legacy)< 1 %
• Scatter Plot (legacy)< 1 %
• Color Manager< 1 %
• Shape Manager< 1 %
• Fingerprint Bayesian Learner< 1 %
• ColumnTextConverter< 1 %
• MISSING Generate 2D Coordinates< 1 %
• TimeDelay Loop Start< 1 %
• k-Medoids< 1 %
• JavaScript Conditional Box Plot< 1 %
• Call Local Workflow< 1 %
• String Matcher< 1 %
• Document Data Extractor< 1 %
• Document Viewer< 1 %
• Weka Cluster Assigner (3.7)< 1 %
• Weka Predictor (3.7)< 1 %
• External Tool (Labs)< 1 %
• Value Filter (legacy)< 1 %
• ROC Curve (JavaScript)< 1 %
• Trackmate Tracker< 1 %
• Python Predictor< 1 %
• Python View< 1 %
• Column Filter QuickForm (legacy)< 1 %
• Table Difference Checker< 1 %
• String to Date/Time (legacy)< 1 %
• Dumb Joiner< 1 %
• Remove Empty Rows< 1 %
• NameToStructure< 1 %
• Ceres Fingerprint< 1 %
• CIR< 1 %
• Ceres Substructure Matcher< 1 %
• Properties< 1 %
• Atom Type Hologrammer (Beta)< 1 %
• WhichCyp 1.2< 1 %
• MLFER Descriptors< 1 %
• Transformation Applier< 1 %
• Element Filter< 1 %
• Sugar Remover< 1 %
• RDKit Fingerprint Writer< 1 %
• RDKit Molecule Highlighting< 1 %
• RDKit SMILES Headers< 1 %
• CIR< 1 %
• Proteax as_pln< 1 %
• SeeSAR Interactive GUI< 1 %
• Sdf to Mol2< 1 %
• Groebke-Blackburn-Bienayme< 1 %
• Filter Duplicates< 1 %
• Fingerprint Clustering< 1 %
• MOE Fingerprints< 1 %
• Launch MOE< 1 %
• Murcko Framework< 1 %
• Forge Build k Nearest Neighbor (kNN)< 1 %
• Forge Score Activity Atlas< 1 %
• Forge Score Field QSAR< 1 %
• Forge Molecule Viewer< 1 %
• ReaxysLookup< 1 %
• Atom Replacer< 1 %
• Formula Filter< 1 %
• Fingerprint Similarity< 1 %
• InChI Generator< 1 %
• Tautomer Generator< 1 %
• Apply MDM Model< 1 %
• Dock In MVD< 1 %
• MolCenters< 1 %
• MolCluster< 1 %
• MolScreen< 1 %
• MolStandardize< 1 %
• PIBR Wash Structure< 1 %
• Conformer and Tautomer Predictor< 1 %
• AutoQSAR Build Model< 1 %
• AutoQSAR Predict< 1 %
• CombiGlide Library Enumeration< 1 %
• ConfGen< 1 %
• Desalter< 1 %
• Fragment Joiner< 1 %
• Hierarchical Clustering Report< 1 %
• Export to LiveDesign< 1 %
• MacroModel Conformational Search< 1 %
• Phase Screening< 1 %
• Premin< 1 %
• Property Filter (Propfilter)< 1 %
• REOS Filter< 1 %
• Tautomerizer< 1 %
• Glide XP Visualizer< 1 %
• Speedy SMILES Explicit Chirality Filter< 1 %
• Fingerprint From Counts list< 1 %
• Loop End (3 ports)< 1 %
• Chunk Loop Run-to-time Loop Start< 1 %
• MMP Molecule Splitter (RDKit)< 1 %
• Fragments to MMPs< 1 %
• Append Plate Well IDs< 1 %
• BrunsWatsonDemerit< 1 %
• Fast Tanimoto< 1 %
• FRP< 1 %
• Range Filter< 1 %
• R Snippet< 1 %
• BCUT< 1 %
• Conformers< 1 %
• Geometrical Descriptors< 1 %
• H Bond Donor/Acceptor< 1 %
• Heavy Scalar Descriptor< 1 %
• HNMR Prediction< 1 %
• Join Reaction< 1 %
• Markush Composer< 1 %
• Polarizability< 1 %
• Polar Surface Area< 1 %
• Tautomers< 1 %
• Topology Analysis< 1 %
• Uni Reactor (By Input)< 1 %
• Chemical Search< 1 %
• GPCRDB Structure-ligand interactions< 1 %
• CIR< 1 %
• Atom Selector< 1 %
• String to Molecule< 1 %
• Element Selector< 1 %
• Create Collection Column< 1 %
• File Meta Info (legacy)< 1 %
• Inject Variables (Data)< 1 %
• Table Row to Variable< 1 %
• Variable to Table Row< 1 %
• Database Looping< 1 %
• Interval Loop Start< 1 %
• Variable Loop End< 1 %
• Naive Bayes Learner< 1 %
• PNN Predictor< 1 %
• k-Means< 1 %
• K Nearest Neighbor< 1 %
• PCA< 1 %
• Logistic Regression Learner< 1 %
• PCA< 1 %
• Random Forest Learner< 1 %
• Random Forest Predictor< 1 %
• PMML Validation Data Appender< 1 %
• Auto-Binner (Apply)< 1 %
• Numeric Binner< 1 %
• Column Comparator< 1 %
• Column to Grid< 1 %
• Linear Correlation< 1 %
• Constant Value Column Filter< 1 %
• Row Filter (Labs)< 1 %
• Missing Value< 1 %
• Number to String (PMML)< 1 %
• String to Number (PMML)< 1 %
• Reference Column Resorter< 1 %
• RowID< 1 %
• Rule Engine Variable (Dictionary)< 1 %
• Interactive Pie chart (legacy)< 1 %
• ROC Curve (legacy)< 1 %
• Workflow Executor< 1 %
• SDF Inserter< 1 %
• SDF Writer< 1 %
• DB Table Creator< 1 %
• 2D Density Plot (Plotly)< 1 %
• Box Plot< 1 %
• Histogram< 1 %
• Histogram (JavaScript)< 1 %
• Pharmacophores Viewer< 1 %
• Stacked Area Chart< 1 %
• Violin Plot (Plotly)< 1 %
• Variable Expressions< 1 %
• DL4J Feedforward Predictor (Regression) (legacy)< 1 %
• JPython Script 1:1 (Legacy)< 1 %
• Rule Viewer (local) (Legacy)< 1 %
• Open TIBCO Spotfire< 1 %
• DF< 1 %
• Scatter Plot (JavaScript)< 1 %
• Column Filter Widget< 1 %
• Table to JSON< 1 %
• Image Viewer< 1 %
• Call Workflow (Table Based)< 1 %
• Python Script (1⇒2)< 1 %
• Python Edit Variable (legacy)< 1 %
• Python View (legacy)< 1 %
• R Learner< 1 %
• Data to Report (BIRT)< 1 %
• String to Date&Time< 1 %
• Standardizer< 1 %
• Substructure Matcher< 1 %
• Submit< 1 %
• Orion Model Learner< 1 %
• SMARTCyp 2.4.2< 1 %
• Transformation Applier (V2)< 1 %
• Orion Model Learner< 1 %
• Depiction< 1 %
• OPSIN< 1 %
• Sum Formula< 1 %
• Bash< 1 %
• Presto Request< 1 %
• ROCColoring< 1 %
• Clustering-Kohonen< 1 %
• Largest Fragment< 1 %
• Gaussian< 1 %
• Sequence Convert< 1 %
• Forge Score Machine Learning< 1 %
• Aromatizer< 1 %
• Gold Desktop Input< 1 %
• Omega2< 1 %
• Library Filter< 1 %
• Fingerprint Similarity Calculator< 1 %
• Table Merger< 1 %
• ReadFilesToText< 1 %
• Desmond System Builder< 1 %
• Fragments from Molecules< 1 %
• LiveDesign Input< 1 %
• Neutralizer< 1 %
• String-to-Type< 1 %
• TIBCO Spotfire File Writer< 1 %
• RMSD Conformer List Filter< 1 %
• PDB Loader< 1 %
• Number Formatter< 1 %
• Charge< 1 %
• Markush Enumeration< 1 %
• Pharmacophore Fingerprint< 1 %
• Set Atom Selection< 1 %
• Similarity Calculator< 1 %
• Variable to Table Row< 1 %
• Table Creator< 1 %
• Recursive Loop Start< 1 %
• Scorer< 1 %
• Scorer< 1 %
• Category to Number (Apply)< 1 %
• Row Splitter (Labs)< 1 %
• Table Difference Finder< 1 %
• Conditional Box Plot (legacy)< 1 %
• DB Insert< 1 %
• DB Writer< 1 %
• Random Label Assigner< 1 %
• Bar Chart< 1 %
• JPython Function (Legacy)< 1 %
• Term to Structure< 1 %
• Column Selection Configuration< 1 %
• Range Slider Filter Definition< 1 %
• Line Plot (JavaScript)< 1 %
• Date&Time Widget< 1 %
• JSON Reader< 1 %
• Score Erosion< 1 %
• Webpage Retriever< 1 %
• Element Splitter< 1 %
• Fragment Fingerprint< 1 %
• Validation and Normalisation (V3)< 1 %
• Ceres Pattern Matcher (OB)< 1 %
• JoinSorted< 1 %