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/********************************************************************** |
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fingerprint.cpp - Implementation of fingerpring base class and fastsearching |
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|
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Copyright (C) 2005 by Chris Morley |
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|
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This file is part of the Open Babel project. |
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For more information, see <http://openbabel.sourceforge.net/> |
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|
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This program is free software; you can redistribute it and/or modify |
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it under the terms of the GNU General Public License as published by |
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the Free Software Foundation version 2 of the License. |
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|
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This program is distributed in the hope that it will be useful, |
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but WITHOUT ANY WARRANTY; without even the implied warranty of |
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MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the |
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GNU General Public License for more details. |
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***********************************************************************/ |
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|
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#include "config.h" |
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#include <vector> |
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#include <algorithm> |
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|
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#if HAVE_IOSTREAM |
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#include <iostream> |
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#elif HAVE_IOSTREAM_H |
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#include <iostream.h> |
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#endif |
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|
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#if HAVE_FSTREAM |
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#include <fstream> |
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#elif HAVE_FSTREAM_H |
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#include <fstream.h> |
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#endif |
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#include <vector> |
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|
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#include "fingerprint.hpp" |
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#include "oberror.hpp" |
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|
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using namespace std; |
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namespace OpenBabel { |
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|
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OBFingerprint* OBFingerprint::_pDefault; //static variable |
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const unsigned int OBFingerprint::bitsperint = 8 * sizeof(unsigned int); |
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int OBFingerprint::rubbish = 666; |
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|
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void OBFingerprint::SetBit(vector<unsigned int>& vec, unsigned int n) |
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{ |
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vec[n/Getbitsperint()] |= (1 << (n % Getbitsperint())); |
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} |
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|
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//////////////////////////////////////// |
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void OBFingerprint::Fold(vector<unsigned int>& vec, unsigned int nbits) |
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{ |
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while(vec.size()*Getbitsperint()/2 >= nbits) |
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vec.erase(transform(vec.begin(),vec.begin()+vec.size()/2, |
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vec.begin()+vec.size()/2, vec.begin(), bit_or()), vec.end()); |
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} |
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|
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//////////////////////////////////////// |
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bool OBFingerprint::GetNextFPrt(std::string& id, OBFingerprint*& pFPrt) |
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{ |
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Fptpos iter; |
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if(id.empty()) |
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iter=FPtsMap().begin(); |
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else |
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{ |
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iter=FPtsMap().find(id); |
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if(iter!=FPtsMap().end()) |
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++iter; |
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} |
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if(iter==FPtsMap().end()) |
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return false; |
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id = iter->first; |
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pFPrt = iter->second; |
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return true; |
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} |
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|
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OBFingerprint* OBFingerprint::FindFingerprint(string& ID) |
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{ |
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if(ID.empty()) |
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return _pDefault; |
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Fptpos iter = FPtsMap().find(ID); |
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if(iter==FPtsMap().end()) |
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return NULL; |
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else |
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return iter->second; |
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} |
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|
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double OBFingerprint::Tanimoto(const vector<unsigned int>& vec1, const vector<unsigned int>& vec2) |
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{ |
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//Independent of sizeof(unsigned int) |
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if(vec1.size()!=vec2.size()) |
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return -1; //different number of bits |
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int andbits=0, orbits=0; |
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for (unsigned i=0;i<vec1.size();++i) |
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{ |
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int andfp = vec1[i] & vec2[i]; |
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int orfp = vec1[i] | vec2[i]; |
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//Count bits |
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for(;andfp;andfp=andfp<<1) |
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if(andfp<0) ++andbits; |
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for(;orfp;orfp=orfp<<1) |
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if(orfp<0) ++orbits; |
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} |
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return((double)andbits/(double)orbits); |
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} |
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|
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//*****************************************************************8 |
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/*! |
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|
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*/ |
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bool FastSearch::Find(OBBase* pOb, vector<unsigned int>& SeekPositions, |
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unsigned int MaxCandidates) |
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{ |
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///Finds chemical objects in datafilename (which must previously have been indexed) |
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///that have all the same bits set in their fingerprints as in the fingerprint of |
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///a pattern object. (Usually a substructure search in molecules.) |
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///The type of fingerprint and its degree of folding does not have to be specified |
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///here because the values in the index file are used. |
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///The positions of the candidate matching molecules in the original datafile are returned. |
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|
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vector<unsigned int> vecwords; |
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_pFP->GetFingerprint(pOb,vecwords, _index.header.words * OBFingerprint::Getbitsperint()); |
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|
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vector<unsigned int>candidates; //indices of matches from fingerprint screen |
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candidates.reserve(MaxCandidates); |
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|
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unsigned int dataSize = _index.header.nEntries; |
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// GetFingerprint(mol, vecwords, _index.header.words, _index.header.fptype); |
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|
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unsigned int words = _index.header.words; |
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unsigned int* nextp = &_index.fptdata[0]; |
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unsigned int* ppat0 = &vecwords[0]; |
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register unsigned int* p; |
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register unsigned int* ppat; |
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register unsigned int a; |
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unsigned int i; // need address of this, can't be register |
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for(i=0;i<dataSize; i++) //speed critical section |
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{ |
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p=nextp; |
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nextp += words; |
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ppat=ppat0; |
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a=0; |
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while(p<nextp) |
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{ |
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if ( (a=((*ppat) & (*p++)) ^ (*ppat++)) ) break; |
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} |
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if(!a) |
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{ |
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candidates.push_back(i); |
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if(candidates.size()>=MaxCandidates) |
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break; |
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} |
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} |
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|
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if(i<_index.header.nEntries) //premature end to search |
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{ |
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#ifdef HAVE_SSTREAM |
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stringstream errorMsg; |
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#else |
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strstream errorMsg; |
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#endif |
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errorMsg << "Stopped looking after " << i << " molecules." << endl; |
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obErrorLog.ThrowError(__func__, errorMsg.str(), obWarning); |
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} |
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|
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vector<unsigned int>::iterator itr; |
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for(itr=candidates.begin();itr!=candidates.end();itr++) |
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{ |
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SeekPositions.push_back(_index.seekdata[*itr]); |
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} |
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return true; |
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} |
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|
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///////////////////////////////////////////////////////// |
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bool FastSearch::FindSimilar(OBBase* pOb, multimap<double, unsigned int>& SeekposMap, |
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double MinTani) |
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{ |
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vector<unsigned int> targetfp; |
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_pFP->GetFingerprint(pOb,targetfp, _index.header.words * OBFingerprint::Getbitsperint()); |
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|
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unsigned int words = _index.header.words; |
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unsigned int dataSize = _index.header.nEntries; |
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unsigned int* nextp = &_index.fptdata[0]; |
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register unsigned int* p; |
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register unsigned int i; |
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for(i=0;i<dataSize; i++) //speed critical section |
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{ |
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p=nextp; |
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nextp += words; |
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double tani = OBFingerprint::Tanimoto(targetfp,p); |
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if(tani>MinTani) |
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SeekposMap.insert(pair<const double, unsigned int>(tani,_index.seekdata[i])); |
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} |
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return true; |
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} |
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|
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///////////////////////////////////////////////////////// |
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bool FastSearch::FindSimilar(OBBase* pOb, multimap<double, unsigned int>& SeekposMap, |
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int nCandidates) |
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{ |
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///If nCandidates is zero or omitted the original size of the multimap is used |
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if(nCandidates) |
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{ |
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//initialise the multimap with nCandidate zero entries |
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SeekposMap.clear(); |
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int i; |
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for(i=0;i<nCandidates;++i) |
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SeekposMap.insert(pair<const double, unsigned int>(0,0)); |
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} |
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else if(SeekposMap.size()==0) |
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return false; |
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|
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vector<unsigned int> targetfp; |
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_pFP->GetFingerprint(pOb,targetfp, _index.header.words * OBFingerprint::Getbitsperint()); |
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|
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unsigned int words = _index.header.words; |
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unsigned int dataSize = _index.header.nEntries; |
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unsigned int* nextp = &_index.fptdata[0]; |
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register unsigned int* p; |
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register unsigned int i; |
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for(i=0;i<dataSize; i++) //speed critical section |
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{ |
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p=nextp; |
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nextp += words; |
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double tani = OBFingerprint::Tanimoto(targetfp,p); |
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if(tani>SeekposMap.begin()->first) |
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{ |
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SeekposMap.insert(pair<const double, unsigned int>(tani,_index.seekdata[i])); |
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SeekposMap.erase(SeekposMap.begin()); |
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} |
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} |
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return true; |
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} |
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|
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///////////////////////////////////////////////////////// |
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string FastSearch::ReadIndex(istream* pIndexstream) |
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{ |
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//Reads fs index from istream into member variables |
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_index.Read(pIndexstream); |
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|
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_pFP = _index.CheckFP(); |
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if(!_pFP) |
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*(_index.header.datafilename) = '\0'; |
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|
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return _index.header.datafilename; //will be empty on error |
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} |
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|
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////////////////////////////////////////////////////////// |
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bool FptIndex::Read(istream* pIndexstream) |
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{ |
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pIndexstream->read((char*)&(header), sizeof(FptIndexHeader)); |
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pIndexstream->seekg(header.headerlength);//allows header length to be changed |
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if(pIndexstream->fail() || header.headerlength != sizeof(FptIndexHeader)) |
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{ |
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*(header.datafilename) = '\0'; |
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return false; |
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} |
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|
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unsigned int nwords = header.nEntries * header.words; |
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fptdata.resize(nwords); |
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seekdata.resize(header.nEntries); |
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|
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pIndexstream->read((char*)&(fptdata[0]), sizeof(unsigned int) * nwords); |
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pIndexstream->read((char*)&(seekdata[0]), sizeof(unsigned int) * header.nEntries); |
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|
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if(pIndexstream->fail()) |
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{ |
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*(header.datafilename) = '\0'; |
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return false; |
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} |
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return true; |
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} |
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|
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////////////////////////////////////////////////////////// |
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OBFingerprint* FptIndex::CheckFP() |
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{ |
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//check that fingerprint type is available |
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string tempFP(header.fpid); |
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OBFingerprint* pFP = OBFingerprint::FindFingerprint(tempFP); |
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if(!pFP) |
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{ |
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#ifdef HAVE_SSTREAM |
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stringstream errorMsg; |
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#else |
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strstream errorMsg; |
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#endif |
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errorMsg << "Index has Fingerprints of type '" << header.fpid |
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<< " which is not currently loaded." << endl; |
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obErrorLog.ThrowError(__func__, errorMsg.str(), obError); |
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} |
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return pFP; //NULL if not available |
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} |
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|
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//******************************************************* |
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FastSearchIndexer::FastSearchIndexer(string& datafilename, ostream* os, |
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std::string& fpid, int FptBits) |
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{ |
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///Starts indexing process |
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_indexstream = os; |
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_nbits=FptBits; |
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_pindex= new FptIndex; |
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_pindex->header.headerlength = sizeof(FptIndexHeader); |
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strncpy(_pindex->header.fpid,fpid.c_str(),15); |
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strncpy(_pindex->header.datafilename, datafilename.c_str(), 255); |
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|
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//check that fingerprint type is available |
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_pFP = _pindex->CheckFP(); |
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} |
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|
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///////////////////////////////////////////////////////////// |
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FastSearchIndexer::FastSearchIndexer(FptIndex* pindex, std::ostream* os) |
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{ |
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//Uses existing index |
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_indexstream = os; |
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_pindex = pindex; |
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_nbits = _pindex->header.words * OBFingerprint::Getbitsperint(); |
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|
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//check that fingerprint type is available |
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_pFP = _pindex->CheckFP(); |
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} |
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|
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///////////////////////////////////////////////////////////// |
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FastSearchIndexer::~FastSearchIndexer() |
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{ |
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///Saves index file |
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_pindex->header.nEntries = _pindex->seekdata.size(); |
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_indexstream->write((const char*)&_pindex->header, sizeof(FptIndexHeader)); |
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_indexstream->write((const char*)&_pindex->fptdata[0], _pindex->fptdata.size()*sizeof(unsigned int)); |
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_indexstream->write((const char*)&_pindex->seekdata[0], _pindex->seekdata.size()*sizeof(unsigned int)); |
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if(!_indexstream) |
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obErrorLog.ThrowError(__func__, |
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"Difficulty writing index", obWarning); |
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delete _pindex; |
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} |
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|
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/////////////////////////////////////////////////////////////// |
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bool FastSearchIndexer::Add(OBBase* pOb, streampos seekpos) |
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{ |
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///Adds a fingerprint |
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|
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vector<unsigned int> vecwords; |
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if(!_pFP) |
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return false; |
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if(_pFP->GetFingerprint(pOb, vecwords, _nbits)) |
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{ |
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_pindex->header.words = vecwords.size(); //Use size as returned from fingerprint |
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for(unsigned int i=0;i<_pindex->header.words;i++) |
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_pindex->fptdata.push_back(vecwords[i]); |
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_pindex->seekdata.push_back(seekpos); |
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return true; |
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} |
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obErrorLog.ThrowError(__func__, "Failed to make a fingerprint", obWarning); |
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return false; |
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} |
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|
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/*! |
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\class OBFingerprint |
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These fingerprints are condensed representation of molecules (or other objects) |
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as a list of boolean values (actually bits in a vector<unsigned>) with length |
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of a power of 2. The main motivation is for fast searching of data sources |
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containing large numbers of molecules (up to several million). OpenBabel |
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provides some routines which can search text files containing lists of molecules |
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in any format. See the documentation on the class FastSearch. |
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|
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There are descriptions of molecular fingerprints at <br> |
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http://www.daylight.com/dayhtml/doc/theory/theory.finger.html) and <br> |
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http://www.mesaac.com/Fingerprint.htm <br> |
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Many methods of preparing fingerprints have been described, but the type supported |
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currently in OpenBabel has each bit representing a substructure (or other |
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molecular property). If a substructure is present in the molecule, then a |
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particular bit is set to 1. But because the hashing method may also map other |
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substructures to the same bit, a match does not guarantee that a particular |
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substructure is present; there may be false positives. However, with proper design, |
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a large fraction of irrelevant molecules in a data set can be eliminated in a |
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fast search with boolean methods on the fingerprints. |
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It then becomes feasible to make a definitive substructure search by |
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conventional methods on this reduced list even if it is slow. |
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|
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OpenBabel provides a framework for applying new types of fingerprints without |
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changing any existing code. They are derived from OBFingerprint and the |
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source file is just compiled with the rest of OpenBabel. Alternatively, |
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they can be separately compiled as a DLL or shared library and discovered |
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when OpenBabel runs. |
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|
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Fingerprints derived from this abstract base class OBFingerprint can be for any |
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object derived from OBBase (not just for OBMol). |
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Each derived class provides an ID as a string and OBFingerprint keeps a map of |
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these to provides a pointer to the class when requested in FindFingerprint. |
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|
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<h4>-- To define a fingerprint type --</h4> |
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The classes derived form OBFingerprint are required to provide |
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a GetFingerprint() routine and a Description() routine |
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\code |
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class MyFpType : OBFingerprint |
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{ |
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MyFpType(const char* id) : OBFingerprint(id){}; |
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virtual bool GetFingerprint(OBBase* pOb, vector<unsigned int>& fp, int nbits) |
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{ |
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//Convert pOb to the required type, usually OBMol |
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OBMol* pmol = dynamic_cast<OBMol*>(pOb); |
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fp.resize(required_number_of_words); |
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... |
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use SetBit(fp,n); to set the nth bit |
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|
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if(nbits) |
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Fold(fp, nbits); |
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} |
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virtual const char* Description(){ return "Some descriptive text";} |
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... |
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}; |
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\endcode |
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//Declare a global instance with the ID you will use in -f options to specify its use. |
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\code |
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MyFpType theMyFpType("myfpID"); |
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\endcode |
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|
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<h4>-- To obtain a fingerprint --</h4> |
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\code |
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OBMol mol; |
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... |
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vector<unsigned int> fp; |
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OBFingerprint::GetDefault()->GetFingerprint(&mol, fp); //gets default size of fingerprint |
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\endcode |
| 425 |
or |
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\code |
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vector<unsigned int> fp; |
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OBFingerPrint* pFP = OBFingerprint::FindFingerprint("myfpID"); |
| 429 |
...and maybe... |
| 430 |
pFP->GetFingerprint(&mol,fp, 128); //fold down to 128bits if was originally larger |
| 431 |
\endcode |
| 432 |
|
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<h4>-- To print a list of available fingerprint types --</h4> |
| 434 |
\code |
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std::string id; |
| 436 |
OBFingerPrint* pFPrt=NULL; |
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while(OBFingerprint::GetNextFPrt(id, pFPrt)) |
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{ |
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cout << id << " -- " << pFPrt->Description() << endl; |
| 440 |
} |
| 441 |
\endcode |
| 442 |
|
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|
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Fingerprints are handled as vector<unsigned int> so that the number of bits |
| 445 |
in this vector and their order will be platform and compiler |
| 446 |
dependent, because of size of int and endian differences. Use fingerprints |
| 447 |
(and fastsearch indexes containing them) only for comparing with other |
| 448 |
fingerprints prepared on the same machine. |
| 449 |
|
| 450 |
The FingerprintFormat class is an output format which displays fingerprints |
| 451 |
as hexadecimal. When multiple molecules are supplied it will calculate the |
| 452 |
Tanimoto coefficient from the first molecule to each of the others. It also |
| 453 |
shows whether the first molecule is a possible substructure to all the others, |
| 454 |
i.e. whether all the bits set in the fingerprint for the first molecule are |
| 455 |
set in the fingerprint of the others. To display hexadecimal information when |
| 456 |
multiple molecules are provided it is necessay to use the -xh option. |
| 457 |
|
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To see a list of available format types, type babel -F on the command line. |
| 459 |
The -xF option of the FingerprintFormat class also provides this output, but due |
| 460 |
to a quirk in the way the program works, it is necessary to have a valid input |
| 461 |
molecule for this option to work. |
| 462 |
*/ |
| 463 |
|
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/*! \class FastSearch |
| 465 |
The FastSearch class searches an index to a datafile containing a list of molecules |
| 466 |
(or other objects) prepared by FastSearchIndexer. |
| 467 |
|
| 468 |
OpenBabel can also search files for molecules containing a substructure specified |
| 469 |
by a SMARTS string, using OBSmartsPattern or from the command line: |
| 470 |
\code |
| 471 |
babel datafile.xxx -outfile.yyy -sSMARTS |
| 472 |
\endcode |
| 473 |
But when the data file contains more than about 10,000 molecules this becomes |
| 474 |
rather too slow to be used interactively. To do it more quickly, an index |
| 475 |
of the molecules containing their fingerprints (see OBFingerprint) is prepared using |
| 476 |
FastSearchIndexer. The indexing process may take a long time but only has to |
| 477 |
be done once. The index can be searched very quickly with FastSearch. Because |
| 478 |
of the nature of fingerprints a match to a bit does not guarantee |
| 479 |
the presence of a particular substructure or other molecular property, so that |
| 480 |
a definitive answer may require a subsequent search of the (much reduced) list |
| 481 |
of candidates by another method (like OBSmartsPattern). |
| 482 |
|
| 483 |
Note that the index files are not portable. They need to be prepared on the |
| 484 |
computer that will acess them. |
| 485 |
|
| 486 |
<h4>Using FastSearch and FastSearchIndexer in a program</h4> |
| 487 |
|
| 488 |
The index has two tables: |
| 489 |
- an array of fingerprints of the molecules |
| 490 |
- an array of the seek positions in the datasource file of all the molecules |
| 491 |
|
| 492 |
<h4>To prepare an fastsearch index file:</h4> |
| 493 |
- Open an ostream to the index file. |
| 494 |
- Make a FastSearchIndexer object on the heap or the stack, passing in as parameters: |
| 495 |
- the datafile name, the indexfile stream, |
| 496 |
- the id of the fingerprint type to be used, |
| 497 |
- the number of bits the fingerprint is to be folded down to, If it is to be left |
| 498 |
unfolded, set fpid to 0 or do not specify it. |
| 499 |
. |
| 500 |
- For each molecule, call Add() with its pointer and its position in the datafile.<br> |
| 501 |
Currently the std::streampos value is implicitly cast to unsigned int so that |
| 502 |
for 32bit machines the datafile has to be no longer than about 2Gbyte. |
| 503 |
- The index file is written when the FastSearchIndexer object is deleted or goes out |
| 504 |
of scope. |
| 505 |
|
| 506 |
<h4>To search in a fastsearch index file</h4> |
| 507 |
|
| 508 |
- Open a std::istream to the indexfile (in binary mode on some systems) |
| 509 |
- Make a FastSearch object, read the index and open the datafile whose |
| 510 |
name it provides |
| 511 |
\code |
| 512 |
ifstream ifs(indexname,ios::binary); |
| 513 |
FastSearch fs; |
| 514 |
string datafilename = fs.ReadIndex(&ifs); |
| 515 |
if(datafilename.empty()/endcode |
| 516 |
return false; |
| 517 |
ifstream datastream(datafilename); |
| 518 |
if(!datastream) |
| 519 |
return false; |
| 520 |
\endcode |
| 521 |
|
| 522 |
<strong>To do a search for molecules which have all the substructure bits the |
| 523 |
OBMol object, patternMol</strong> |
| 524 |
\code |
| 525 |
vector<unsigned int>& SeekPositions; |
| 526 |
if(!fs.Find(patternMol, SeekPositions, MaxCandidates)) |
| 527 |
|
| 528 |
for(itr=SeekPositions.begin();itr!=SeekPositions.end();itr++) |
| 529 |
{ |
| 530 |
datastream.seekg(*itr); |
| 531 |
... read the candidate molecule |
| 532 |
and subject to more rigorous test if necessary |
| 533 |
} |
| 534 |
\endcode |
| 535 |
|
| 536 |
<strong>To do a similarity search based on the Tanimoto coefficient</strong> |
| 537 |
This is defined as: <br> |
| 538 |
<em>Number of bits set in (patternFP & targetFP)/Number of bits in (patternFP | targetFP)</em><br> |
| 539 |
where the boolean operations between the fingerprints are bitwise<br> |
| 540 |
The Tanimoto coefficient has no absolute meaning and depends on |
| 541 |
the design of the fingerprint. |
| 542 |
\code |
| 543 |
multimap<double, unsigned int> SeekposMap; |
| 544 |
// to find n best molecules |
| 545 |
fs.FindSimilar(&patternMol, SeekposMap, n); |
| 546 |
...or |
| 547 |
// to find molecules with Tanimoto coefficient > MinTani |
| 548 |
fs.FindSimilar(&patternMol, SeekposMap, MinTani); |
| 549 |
|
| 550 |
multimap<double, unsigned int>::reverse_iterator itr; |
| 551 |
for(itr=SeekposMap.rbegin();itr!=SeekposMap.rend();++itr) |
| 552 |
{ |
| 553 |
datastream.seekg(itr->second); |
| 554 |
... read the candidate molecule |
| 555 |
double tani = itr->first; |
| 556 |
} |
| 557 |
\endcode |
| 558 |
|
| 559 |
The FastSearchFormat class facilitates the use of these routine from the |
| 560 |
command line or other front end program. For instance: |
| 561 |
|
| 562 |
<strong>Prepare an index:</strong> |
| 563 |
\code |
| 564 |
babel datafile.xxx index.fs |
| 565 |
\endcode |
| 566 |
or |
| 567 |
\code |
| 568 |
babel datafile.xxx -ofs namedindex |
| 569 |
\endcode |
| 570 |
With options you can specify: |
| 571 |
- which type of fingerprint to be used, e.g. -xfFP2, |
| 572 |
- whether it is folded to a specified number of bits, e.g. -xn128 |
| 573 |
(which should be a power of2) |
| 574 |
- whether to pre-select the molecules which are indexed: |
| 575 |
- by structure e.g only ethers and esters, -sCOC |
| 576 |
- by excluding molecules with bezene rings, -vc1ccccc1 |
| 577 |
- by position in the datafile e.g. only mols 10 to 90, -f10 -l90 |
| 578 |
. |
| 579 |
<strong>Substructure search</strong> in a previously prepared index file |
| 580 |
\code |
| 581 |
babel index.fs outfile.yyy -sSMILES |
| 582 |
\endcode |
| 583 |
The datafile can also be used as the input file, provided the input format is specified as fs |
| 584 |
\code |
| 585 |
babel datafile.xxx outfile.yyy -sSMILES -ifs |
| 586 |
\endcode |
| 587 |
A "slow" search not using fingerprints would be done on the same data by omitting -ifs. |
| 588 |
A "slow" search can use SMARTS strings, but the fast search is restricted |
| 589 |
to the subset which is valid SMILES. |
| 590 |
|
| 591 |
With the -S option, the target can be specified as a molecule in a file of any format |
| 592 |
\code |
| 593 |
babel datafile.xxx outfile.yyy -Spattern_mol.zzz -ifs |
| 594 |
\endcode |
| 595 |
These searches have two stages: a fingerprint search which produces |
| 596 |
a number of candidate molecules and a definitive search which selects |
| 597 |
from these using SMARTS pattern matching. The maximum number of candidates |
| 598 |
is 4000 by default but you can change this with an option |
| 599 |
e.g. -al 8000 (Note that you need the space between l and the number.) |
| 600 |
If the fingerprint search reaches the maximum number it will not |
| 601 |
look further and will tell you at what stage it stopped. |
| 602 |
|
| 603 |
<strong>Similarity search</strong> in a previously prepared index file<br> |
| 604 |
This rather done (rather than a substructure search) if the -at option is used, |
| 605 |
\code |
| 606 |
babel datafile.xxx outfile.yyy -sSMILES -ifs -at0.7 |
| 607 |
\endcode |
| 608 |
for instance |
| 609 |
- -at0.7 will recover all molecules with Tanimoto greater than 0.7 |
| 610 |
- -at15 (no decimal point) will recover the 15 molecules with largest coefficients. |
| 611 |
- -aa will add the Tanimoto coefficient to the titles of the output molecules. |
| 612 |
|
| 613 |
All stages, the indexing, the interpretation of the SMILES string in the -s option, |
| 614 |
the file in the -S option and the final SMARTS filter convert to OBMol and apply |
| 615 |
ConvertDativeBonds(). This ensures thatforms such as[N+]([O-])=O and N(=O)=O |
| 616 |
are recognized as chemically identical. |
| 617 |
*/ |
| 618 |
|
| 619 |
}//Openbabel |
| 620 |
|
| 621 |
//! \file fingerprint.cpp |
| 622 |
//! \brief Definitions for OBFingerprint base class and fastsearch classes |