Logo Search packages:      
Sourcecode: cdk version File versions  Download package


/* $Revision: 11674 $ $Author: rajarshi $ $Date: 2008-07-20 22:05:08 -0400 (Sun, 20 Jul 2008) $
 * Copyright (C) 2008 Rajarshi Guha <rajarshi@users.sourceforge.net>
 * Contact: cdk-devel@lists.sourceforge.net
 * This program is free software; you can redistribute it and/or
 * modify it under the terms of the GNU Lesser General Public License
 * as published by the Free Software Foundation; either version 2.1
 * of the License, or (at your option) any later version.
 * All we ask is that proper credit is given for our work, which includes
 * - but is not limited to - adding the above copyright notice to the beginning
 * of your source code files, and to any copyright notice that you may distribute
 * with programs based on this work.
 * This program is distributed in the hope that it will be useful,
 * but WITHOUT ANY WARRANTY; without even the implied warranty of
 * GNU Lesser General Public License for more details.
 * You should have received a copy of the GNU Lesser General Public License
 * along with this program; if not, write to the Free Software
 * Foundation, Inc., 51 Franklin St, Fifth Floor, Boston, MA 02110-1301 USA.
package org.openscience.cdk.fingerprint;

import org.openscience.cdk.annotations.TestClass;
import org.openscience.cdk.annotations.TestMethod;
import org.openscience.cdk.config.fragments.EStateFragments;
import org.openscience.cdk.exception.CDKException;
import org.openscience.cdk.interfaces.IAtomContainer;
import org.openscience.cdk.smiles.smarts.SMARTSQueryTool;

import java.util.BitSet;

 * This fingerprinter generates 79 bit fingerprints using the E-State fragments.
 * <p>The E-State fragments are those described in {@cdk.cite HALL1995} and the SMARTS
 * patterns were taken from <a href="http://www.rdkit.org">RDKit</a>. Note that this
 * fingerprint simply indicates the presence or occurrence of the fragments. If you need
 * counts of the fragments take a look at {@link org.openscience.cdk.qsar.descriptors.molecular.KierHallSmartsDescriptor},
 * which also lists the substructures corresponding to each bit position.
 * <p>This class assumes that aromaticity perception and atom typing have been performed
 * prior to generating the fingerprint
 * @author Rajarhi Guha
 * @cdk.created 2008-07-23
 * @cdk.keyword fingerprint
 * @cdk.keyword similarity
 * @cdk.keyword estate
 * @cdk.module fingerprint
 * @cdk.githash
00059 public class EStateFingerprinter implements IFingerprinter {

      private static final String[] patterns = EStateFragments.getSmarts();

    public EStateFingerprinter() {

       * Calculates the substructure fingerprint for the given AtomContainer.
00071     public BitSet getFingerprint(IAtomContainer atomContainer) throws CDKException {

        int bitsetLength = patterns.length;
            BitSet fingerPrint = new BitSet(bitsetLength);

        SMARTSQueryTool sqt = new SMARTSQueryTool("C");
        for (int i = 0; i < patterns.length; i++) {
            boolean status = sqt.matches(atomContainer);
            if (status) fingerPrint.set(i, true);
            return fingerPrint;

00086     public int getSize() {
            return patterns.length;


Generated by  Doxygen 1.6.0   Back to index