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Open Source Chemistry Library
/*
* Copyright (c) 1997 - 2016
* Actelion Pharmaceuticals Ltd.
* Gewerbestrasse 16
* CH-4123 Allschwil, Switzerland
*
* All rights reserved.
*
* Redistribution and use in source and binary forms, with or without
* modification, are permitted provided that the following conditions are met:
*
* 1. Redistributions of source code must retain the above copyright notice, this
* list of conditions and the following disclaimer.
* 2. Redistributions in binary form must reproduce the above copyright notice,
* this list of conditions and the following disclaimer in the documentation
* and/or other materials provided with the distribution.
* 3. Neither the name of the the copyright holder nor the
* names of its contributors may be used to endorse or promote products
* derived from this software without specific prior written permission.
*
* THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS "AS IS" AND
* ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED
* WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE
* DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT OWNER OR CONTRIBUTORS BE LIABLE FOR
* ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES
* (INCLUDING, BUT NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES;
* LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND
* ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT
* (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS
* SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
*
*/
package com.actelion.research.chem.descriptor;
import com.actelion.research.chem.Canonizer;
import com.actelion.research.chem.Molecule;
import com.actelion.research.chem.SSSearcherWithIndex;
import com.actelion.research.chem.StereoMolecule;
import com.actelion.research.util.BurtleHasher;
import com.actelion.research.util.datamodel.IntVec;
import java.util.Arrays;
public class DescriptorHandlerHashedCFp extends AbstractDescriptorHandlerFP {
private static final double CORRECTION_FACTOR = 0.6;
private static DescriptorHandlerHashedCFp sDefaultInstance;
private static final int SPHERE_COUNT = 5;
private static final int HASH_BITS = 10;
private static final int HASH_INIT = 13;
private static final int DESCRIPTOR_SIZE = (1 << HASH_BITS);
public static DescriptorHandlerHashedCFp getDefaultInstance() {
synchronized(DescriptorHandlerHashedCFp.class) {
if (sDefaultInstance == null) {
sDefaultInstance = new DescriptorHandlerHashedCFp();
}
}
return sDefaultInstance;
}
public DescriptorInfo getInfo() {
return DescriptorConstants.DESCRIPTOR_HashedCFp;
}
public String getVersion() {
return DescriptorConstants.DESCRIPTOR_HashedCFp.version;
}
/**
* This descriptor requires proper up/down bonds, because it encodes stereo parities.
* If a passed molecule is generated from idcode parsing, make sure that coordinates
* and up/down/bonds are available, i.e. that the IDCodeParser was instantiated with
* the respective option.
*/
public int[] createDescriptor(StereoMolecule mol) {
if (mol ==null)
return null;
mol.ensureHelperArrays(Molecule.cHelperRings);
StereoMolecule fragment = new StereoMolecule(mol.getAtoms(), mol.getBonds());
// byte[] descriptor = new byte[DESCRIPTOR_SIZE];
int len = DESCRIPTOR_SIZE / Integer.SIZE;
IntVec iv = new IntVec(len);
int[] atomList = new int[mol.getAtoms()];
boolean[] atomMask = new boolean[mol.getAtoms()];
for (int rootAtom=0; rootAtom= 1.0f ? 1.0f
: (float)(1.0-Math.pow(1-Math.pow(value, CORRECTION_FACTOR) ,1.0/CORRECTION_FACTOR));
}
public DescriptorHandler getThreadSafeCopy() {
return this;
}
}