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14 <table width="100%" border=0 cellpadding=0 cellspacing=2>
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15 <tr align="left" valign="top"><td width="33%" align="left"><a href="./MolFilesToSD.html" title="MolFilesToSD.html">Previous</a> <a href="./index.html" title="Table of Contents">TOC</a> <a href="./SDFilesToHTML.html" title="SDFilesToHTML.html">Next</a></td><td width="34%" align="middle"><strong>PathLengthFingerprints.pl</strong></td><td width="33%" align="right"><a href="././code/PathLengthFingerprints.html" title="View source code">Code</a> | <a href="./../pdf/PathLengthFingerprints.pdf" title="PDF US Letter Size">PDF</a> | <a href="./../pdfgreen/PathLengthFingerprints.pdf" title="PDF US Letter Size with narrow margins: www.changethemargins.com">PDFGreen</a> | <a href="./../pdfa4/PathLengthFingerprints.pdf" title="PDF A4 Size">PDFA4</a> | <a href="./../pdfa4green/PathLengthFingerprints.pdf" title="PDF A4 Size with narrow margins: www.changethemargins.com">PDFA4Green</a></td></tr>
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16 </table>
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17 </div>
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18 <p>
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19 </p>
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20 <h2>NAME</h2>
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21 <p>PathLengthFingerprints.pl - Generate atom path length based fingerprints for SD files</p>
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22 <p>
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23 </p>
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24 <h2>SYNOPSIS</h2>
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25 <p>PathLengthFingerprints.pl SDFile(s)...</p>
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26 <p>PathLengthFingerprints.pl [<strong>--AromaticityModel</strong> <em>AromaticityModelType</em>]
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27 [<strong>-a, --AtomIdentifierType</strong> <em>AtomicInvariantsAtomTypes</em>]
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28 [<strong>--AtomicInvariantsToUse</strong> <em>"AtomicInvariant1,AtomicInvariant2..."</em>]
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29 [<strong>--FunctionalClassesToUse</strong> <em>"FunctionalClass1,FunctionalClass2..."</em>]
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30 [<strong>--BitsOrder</strong> <em>Ascending | Descending</em>] [<strong>-b, --BitStringFormat</strong> <em>BinaryString | HexadecimalString</em>]
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31 [<strong>--CompoundID</strong> <em>DataFieldName or LabelPrefixString</em>] [<strong>--CompoundIDLabel</strong> <em>text</em>]
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32 [<strong>--CompoundIDMode</strong> <em>DataField | MolName | LabelPrefix | MolNameOrLabelPrefix</em>]
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33 [<strong>--DataFields</strong> <em>"FieldLabel1,FieldLabel2,... "</em>] [<strong>-d, --DataFieldsMode</strong> <em>All | Common | Specify | CompoundID</em>]
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34 [<strong>--DetectAromaticity</strong> <em>Yes | No</em>] [<strong>-f, --Filter</strong> <em>Yes | No</em>] [<strong>--FingerprintsLabel</strong> <em>text</em>]
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35 [<strong>--fold</strong> <em>Yes | No</em>] [<strong>--FoldedSize</strong> <em>number</em>] [<strong>-h, --help</strong>]
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36 [<strong>-i, --IgnoreHydrogens</strong> <em>Yes | No</em>] [<strong>-k, --KeepLargestComponent</strong> <em>Yes | No</em>]
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37 [<strong>-m, --mode</strong> <em>PathLengthBits | PathLengthCount</em>]
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38 [<strong>--MinPathLength</strong> <em>number</em>] [<strong>--MaxPathLength</strong> <em>number</em>] [<strong>-n, --NumOfBitsToSetPerPath</strong> <em>number</em>]
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39 [<strong>--OutDelim</strong> <em>comma | tab | semicolon</em>]
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40 [<strong>--output</strong> <em>SD | FP | text | all</em>] [<strong>-q, --quote</strong> <em>Yes | No</em>] [<strong>-r, --root</strong> <em>RootName</em>]
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41 [<strong>-p, --PathMode</strong> <em>AtomPathsWithoutRings | AtomPathsWithRings | AllAtomPathsWithoutRings | AllAtomPathsWithRings</em>]
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42 [<strong>-s, --size</strong> <em>number</em>] [<strong>-u, --UseBondSymbols</strong> <em>Yes | No</em>] [<strong>--UsePerlCoreRandom</strong> <em>Yes | No</em>]
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43 [<strong>--UseUniquePaths</strong> <em>Yes | No</em>] [<strong>-q, --quote</strong> <em>Yes | No</em>] [<strong>-r, --root</strong> <em>RootName</em>]
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44 [<strong>-v, --VectorStringFormat</strong> <em>IDsAndValuesString | IDsAndValuesPairsString | ValuesAndIDsString | ValuesAndIDsPairsString</em>]
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45 [<strong>-w, --WorkingDir</strong> dirname] SDFile(s)...</p>
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46 <p>
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47 </p>
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48 <h2>DESCRIPTION</h2>
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49 <p>Generate atom path length fingerprints for <em>SDFile(s)</em> and create appropriate SD, FP or
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50 CSV/TSV text file(s) containing fingerprints bit-vector or vector strings corresponding to
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51 molecular fingerprints.</p>
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52 <p>Multiple SDFile names are separated by spaces. The valid file extensions are <em>.sdf</em>
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53 and <em>.sd</em>. All other file names are ignored. All the SD files in a current directory
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54 can be specified either by <em>*.sdf</em> or the current directory name.</p>
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55 <p>The current release of MayaChemTools supports generation of path length fingerprints
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56 corresponding to following <strong>-a, --AtomIdentifierTypes</strong>:</p>
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57 <div class="OptionsBox">
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58 AtomicInvariantsAtomTypes, DREIDINGAtomTypes, EStateAtomTypes,
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59 <br/> FunctionalClassAtomTypes, MMFF94AtomTypes, SLogPAtomTypes,
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60 <br/> SYBYLAtomTypes, TPSAAtomTypes, UFFAtomTypes</div>
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61 <p>Based on the values specified for <strong>-p, --PathMode</strong>, <strong>--MinPathLength</strong> and <strong>--MaxPathLength</strong>,
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62 all appropriate atom paths are generated for each atom in the molecule and collected in a list and
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63 the list is filtered to remove any structurally duplicate paths as indicated by the value of
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64 <strong>--UseUniquePaths</strong> option.</p>
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65 <p>For each atom path in the filtered atom paths list, an atom path string is created using value of
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66 <strong>-a, --AtomIdentifierType</strong> and specified values to use for a particular atom identifier type.
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67 Value of <strong>-u, --UseBondSymbols</strong> controls whether bond order symbols are used during generation
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68 of atom path string. For each atom path, only lexicographically smaller atom path strings are kept.</p>
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69 <p>For <em>PathLengthBits</em> value of <strong>-m, --mode</strong> option, each atom path is hashed to a 32 bit unsigned
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70 integer key using <strong>TextUtil::HashCode</strong> function. Using the hash key as a seed for a random number
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71 generator, a random integer value between 0 and <strong>--Size</strong> is used to set corresponding bits
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72 in the fingerprint bit-vector string. Value of <strong>--NumOfBitsToSetPerPath</strong> option controls the number
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73 of time a random number is generated to set corresponding bits.</p>
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74 <p>For <em> PathLengthCount</em> value of <strong>-m, --mode</strong> option, the number of times an atom path appears
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75 is tracked and a fingerprints count-string corresponding to count of atom paths is generated.</p>
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76 <p>Example of <em>SD</em> file containing path length fingerprints string data:</p>
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77 <div class="OptionsBox">
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78 ... ...
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79 <br/> ... ...
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80 <br/> $$$$
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81 <br/> ... ...
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82 <br/> ... ...
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83 <br/> ... ...
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84 <br/> 41 44 0 0 0 0 0 0 0 0999 V2000
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85 -3.3652 1.4499 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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86 <br/> ... ...
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87 <br/> 2 3 1 0 0 0 0
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88 <br/> ... ...
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89 <br/> M END
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90 <br/> > <CmpdID>
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91 <br/> Cmpd1</div>
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92 <div class="OptionsBox">
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93 > <PathLengthFingerprints>
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94 <br/> FingerprintsBitVector;PathLengthBits:AtomicInvariantsAtomTypes:MinLengt
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95 <br/> h1:MaxLength8;1024;HexadecimalString;Ascending;9c8460989ec8a49913991a66
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96 <br/> 03130b0a19e8051c89184414953800cc2151082844a201042800130860308e8204d4028
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97 <br/> 00831048940e44281c00060449a5000ac80c894114e006321264401600846c050164462
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98 <br/> 08190410805000304a10205b0100e04c0038ba0fad0209c0ca8b1200012268b61c0026a
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99 <br/> aa0660a11014a011d46</div>
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100 <div class="OptionsBox">
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101 $$$$
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102 <br/> ... ...
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103 <br/> ... ...</div>
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104 <p>Example of <em>FP</em> file containing path length fingerprints string data:</p>
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105 <div class="OptionsBox">
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106 #
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107 <br/> # Package = MayaChemTools 7.4
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108 <br/> # ReleaseDate = Oct 21, 2010
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109 <br/> #
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110 <br/> # TimeStamp = Mon Mar 7 15:14:01 2011
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111 <br/> #
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112 <br/> # FingerprintsStringType = FingerprintsBitVector
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113 <br/> #
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114 <br/> # Description = PathLengthBits:AtomicInvariantsAtomTypes:MinLength1:...
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115 <br/> # Size = 1024
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116 <br/> # BitStringFormat = HexadecimalString
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117 <br/> # BitsOrder = Ascending
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118 <br/> #
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119 <br/> Cmpd1 9c8460989ec8a49913991a6603130b0a19e8051c89184414953800cc21510...
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120 <br/> Cmpd2 000000249400840040100042011001001980410c000000001010088001120...
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121 <br/> ... ...
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122 <br/> ... ..</div>
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123 <p>Example of CSV <em>Text</em> file containing pathlength fingerprints string data:</p>
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124 <div class="OptionsBox">
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125 "CompoundID","PathLengthFingerprints"
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126 <br/> "Cmpd1","FingerprintsBitVector;PathLengthBits:AtomicInvariantsAtomTypes
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127 <br/> :MinLength1:MaxLength8;1024;HexadecimalString;Ascending;9c8460989ec8a4
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128 <br/> 9913991a6603130b0a19e8051c89184414953800cc2151082844a20104280013086030
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129 <br/> 8e8204d402800831048940e44281c00060449a5000ac80c894114e006321264401..."
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130 <br/> ... ...
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131 <br/> ... ...</div>
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132 <p>The current release of MayaChemTools generates the following types of path length
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133 fingerprints bit-vector and vector strings:</p>
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134 <div class="OptionsBox">
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135 FingerprintsBitVector;PathLengthBits:AtomicInvariantsAtomTypes:MinLeng
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136 <br/> th1:MaxLength8;1024;BinaryString;Ascending;001000010011010101011000110
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137 <br/> 0100010101011000101001011100110001000010001001101000001001001001001000
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138 <br/> 0010110100000111001001000001001010100100100000000011000000101001011100
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139 <br/> 0010000001000101010100000100111100110111011011011000000010110111001101
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140 <br/> 0101100011000000010001000011000010100011101100001000001000100000000...</div>
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141 <div class="OptionsBox">
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142 FingerprintsBitVector;PathLengthBits:AtomicInvariantsAtomTypes:MinLeng
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143 <br/> th1:MaxLength8;1024;HexadecimalString;Ascending;48caa1315d82d91122b029
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144 <br/> 42861c9409a4208182d12015509767bd0867653604481a8b1288000056090583603078
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145 <br/> 9cedae54e26596889ab121309800900490515224208421502120a0dd9200509723ae89
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146 <br/> 00024181b86c0122821d4e4880c38620dab280824b455404009f082003d52c212b4e6d
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147 <br/> 6ea05280140069c780290c43</div>
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148 <div class="OptionsBox">
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149 FingerprintsVector;PathLengthCount:AtomicInvariantsAtomTypes:MinLength
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150 <br/> 1:MaxLength8;432;NumericalValues;IDsAndValuesPairsString;C.X1.BO1.H3 2
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151 <br/> C.X2.BO2.H2 4 C.X2.BO3.H1 14 C.X3.BO3.H1 3 C.X3.BO4 10 F.X1.BO1 1 N.X
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152 <br/> 2.BO2.H1 1 N.X3.BO3 1 O.X1.BO1.H1 3 O.X1.BO2 2 C.X1.BO1.H3C.X3.BO3.H1
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153 <br/> 2 C.X2.BO2.H2C.X2.BO2.H2 1 C.X2.BO2.H2C.X3.BO3.H1 4 C.X2.BO2.H2C.X3.BO
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154 <br/> 4 1 C.X2.BO2.H2N.X3.BO3 1 C.X2.BO3.H1:C.X2.BO3.H1 10 C.X2.BO3.H1:C....</div>
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155 <div class="OptionsBox">
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156 FingerprintsVector;PathLengthCount:DREIDINGAtomTypes:MinLength1:MaxLen
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157 <br/> gth8;410;NumericalValues;IDsAndValuesPairsString;C_2 2 C_3 9 C_R 22 F_
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158 <br/> 1 N_3 1 N_R 1 O_2 2 O_3 3 C_2=O_2 2 C_2C_3 1 C_2C_R 1 C_2N_3 1 C_2O_3
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159 <br/> 1 C_3C_3 7 C_3C_R 1 C_3N_R 1 C_3O_3 2 C_R:C_R 21 C_R:N_R 2 C_RC_R 2 C
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160 <br/> _RF_ 1 C_RN_3 1 C_2C_3C_3 1 C_2C_R:C_R 2 C_2N_3C_R 1 C_3C_2=O_2 1 C_3C
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161 <br/> _2O_3 1 C_3C_3C_3 5 C_3C_3C_R 2 C_3C_3N_R 1 C_3C_3O_3 4 C_3C_R:C_R ...</div>
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162 <div class="OptionsBox">
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163 FingerprintsVector;PathLengthCount:EStateAtomTypes:MinLength1:MaxLengt
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164 <br/> h8;454;NumericalValues;IDsAndValuesPairsString;aaCH 14 aasC 8 aasN 1 d
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165 <br/> O 2 dssC 2 sCH3 2 sF 1 sOH 3 ssCH2 4 ssNH 1 sssCH 3 aaCH:aaCH 10 aaCH:
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166 <br/> aasC 8 aasC:aasC 3 aasC:aasN 2 aasCaasC 2 aasCdssC 1 aasCsF 1 aasCssNH
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167 <br/> 1 aasCsssCH 1 aasNssCH2 1 dO=dssC 2 dssCsOH 1 dssCssCH2 1 dssCssNH 1
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168 <br/> sCH3sssCH 2 sOHsssCH 2 ssCH2ssCH2 1 ssCH2sssCH 4 aaCH:aaCH:aaCH 6 a...</div>
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169 <div class="OptionsBox">
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170 FingerprintsVector;PathLengthCount:FunctionalClassAtomTypes:MinLength1
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171 <br/> :MaxLength8;404;NumericalValues;IDsAndValuesPairsString;Ar 22 Ar.HBA 1
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172 <br/> HBA 2 HBA.HBD 3 HBD 1 Hal 1 NI 1 None 10 Ar.HBA:Ar 2 Ar.HBANone 1 Ar:
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173 <br/> Ar 21 ArAr 2 ArHBD 1 ArHal 1 ArNone 2 HBA.HBDNI 1 HBA.HBDNone 2 HBA=NI
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174 <br/> 1 HBA=None 1 HBDNone 1 NINone 1 NoneNone 7 Ar.HBA:Ar:Ar 2 Ar.HBA:ArAr
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175 <br/> 1 Ar.HBA:ArNone 1 Ar.HBANoneNone 1 Ar:Ar.HBA:Ar 1 Ar:Ar.HBANone 2 ...</div>
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176 <div class="OptionsBox">
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177 FingerprintsVector;PathLengthCount:MMFF94AtomTypes:MinLength1:MaxLengt
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178 <br/> h8;463;NumericalValues;IDsAndValuesPairsString;C5A 2 C5B 2 C=ON 1 CB 1
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179 <br/> 8 COO 1 CR 9 F 1 N5 1 NC=O 1 O=CN 1 O=CO 1 OC=O 1 OR 2 C5A:C5B 2 C5A:N
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180 <br/> 5 2 C5ACB 1 C5ACR 1 C5B:C5B 1 C5BC=ON 1 C5BCB 1 C=ON=O=CN 1 C=ONNC=O 1
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181 <br/> CB:CB 18 CBF 1 CBNC=O 1 COO=O=CO 1 COOCR 1 COOOC=O 1 CRCR 7 CRN5 1 CR
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182 <br/> OR 2 C5A:C5B:C5B 2 C5A:C5BC=ON 1 C5A:C5BCB 1 C5A:N5:C5A 1 C5A:N5CR ...</div>
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183 <div class="OptionsBox">
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184 FingerprintsVector;PathLengthCount:SLogPAtomTypes:MinLength1:MaxLength
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185 <br/> 8;518;NumericalValues;IDsAndValuesPairsString;C1 5 C10 1 C11 1 C14 1 C
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186 <br/> 18 14 C20 4 C21 2 C22 1 C5 2 CS 2 F 1 N11 1 N4 1 O10 1 O2 3 O9 1 C10C1
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187 <br/> 1 C10N11 1 C11C1 2 C11C21 1 C14:C18 2 C14F 1 C18:C18 10 C18:C20 4 C18
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188 <br/> :C22 2 C1C5 1 C1CS 4 C20:C20 1 C20:C21 1 C20:N11 1 C20C20 2 C21:C21 1
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189 <br/> C21:N11 1 C21C5 1 C22N4 1 C5=O10 1 C5=O9 1 C5N4 1 C5O2 1 CSO2 2 C10...</div>
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190 <div class="OptionsBox">
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191 FingerprintsVector;PathLengthCount:SYBYLAtomTypes:MinLength1:MaxLength
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192 <br/> 8;412;NumericalValues;IDsAndValuesPairsString;C.2 2 C.3 9 C.ar 22 F 1
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193 <br/> N.am 1 N.ar 1 O.2 1 O.3 2 O.co2 2 C.2=O.2 1 C.2=O.co2 1 C.2C.3 1 C.2C.
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194 <br/> ar 1 C.2N.am 1 C.2O.co2 1 C.3C.3 7 C.3C.ar 1 C.3N.ar 1 C.3O.3 2 C.ar:C
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195 <br/> .ar 21 C.ar:N.ar 2 C.arC.ar 2 C.arF 1 C.arN.am 1 C.2C.3C.3 1 C.2C.ar:C
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196 <br/> .ar 2 C.2N.amC.ar 1 C.3C.2=O.co2 1 C.3C.2O.co2 1 C.3C.3C.3 5 C.3C.3...</div>
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197 <div class="OptionsBox">
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198 FingerprintsVector;PathLengthCount:TPSAAtomTypes:MinLength1:MaxLength8
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199 <br/> ;331;NumericalValues;IDsAndValuesPairsString;N21 1 N7 1 None 34 O3 2 O
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200 <br/> 4 3 N21:None 2 N21None 1 N7None 2 None:None 21 None=O3 2 NoneNone 13 N
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201 <br/> oneO4 3 N21:None:None 2 N21:NoneNone 2 N21NoneNone 1 N7None:None 2 N7N
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202 <br/> one=O3 1 N7NoneNone 1 None:N21:None 1 None:N21None 2 None:None:None 20
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203 <br/> None:NoneNone 12 NoneN7None 1 NoneNone=O3 2 NoneNoneNone 8 NoneNon...</div>
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204 <div class="OptionsBox">
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205 FingerprintsVector;PathLengthCount:UFFAtomTypes:MinLength1:MaxLength8;
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206 <br/> 410;NumericalValues;IDsAndValuesPairsString;C_2 2 C_3 9 C_R 22 F_ 1 N_
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207 <br/> 3 1 N_R 1 O_2 2 O_3 3 C_2=O_2 2 C_2C_3 1 C_2C_R 1 C_2N_3 1 C_2O_3 1 C_
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208 <br/> 3C_3 7 C_3C_R 1 C_3N_R 1 C_3O_3 2 C_R:C_R 21 C_R:N_R 2 C_RC_R 2 C_RF_
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209 <br/> 1 C_RN_3 1 C_2C_3C_3 1 C_2C_R:C_R 2 C_2N_3C_R 1 C_3C_2=O_2 1 C_3C_2O_3
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210 <br/> 1 C_3C_3C_3 5 C_3C_3C_R 2 C_3C_3N_R 1 C_3C_3O_3 4 C_3C_R:C_R 1 C_3...</div>
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211 <p>
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212 </p>
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213 <h2>OPTIONS</h2>
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214 <dl>
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215 <dt><strong><strong>--AromaticityModel</strong> <em>MDLAromaticityModel | TriposAromaticityModel | MMFFAromaticityModel | ChemAxonBasicAromaticityModel | ChemAxonGeneralAromaticityModel | DaylightAromaticityModel | MayaChemToolsAromaticityModel</em></strong></dt>
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216 <dd>
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217 <p>Specify aromaticity model to use during detection of aromaticity. Possible values in the current
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218 release are: <em>MDLAromaticityModel, TriposAromaticityModel, MMFFAromaticityModel,
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219 ChemAxonBasicAromaticityModel, ChemAxonGeneralAromaticityModel, DaylightAromaticityModel
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220 or MayaChemToolsAromaticityModel</em>. Default value: <em>MayaChemToolsAromaticityModel</em>.</p>
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221 <p>The supported aromaticity model names along with model specific control parameters
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222 are defined in <strong>AromaticityModelsData.csv</strong>, which is distributed with the current release
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223 and is available under <strong>lib/data</strong> directory. <strong>Molecule.pm</strong> module retrieves data from
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224 this file during class instantiation and makes it available to method <strong>DetectAromaticity</strong>
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225 for detecting aromaticity corresponding to a specific model.</p>
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226 <p>This option is ignored during <em>No</em> value of <strong>--DetectAromaticity</strong> option.</p>
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227 </dd>
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228 <dt><strong><strong>-a, --AtomIdentifierType</strong> <em>AtomicInvariantsAtomTypes | DREIDINGAtomTypes | EStateAtomTypes | FunctionalClassAtomTypes | MMFF94AtomTypes | SLogPAtomTypes | SYBYLAtomTypes | TPSAAtomTypes | UFFAtomTypes</em></strong></dt>
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229 <dd>
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230 <p>Specify atom identifier type to use for assignment of atom types to hydrogen and/or
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231 non-hydrogen atoms during calculation of atom types fingerprints. Possible values in the
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232 current release are: <em>AtomicInvariantsAtomTypes, DREIDINGAtomTypes, EStateAtomTypes,
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233 FunctionalClassAtomTypes, MMFF94AtomTypes, SLogPAtomTypes, SYBYLAtomTypes,
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234 TPSAAtomTypes, UFFAtomTypes</em>. Default value: <em>AtomicInvariantsAtomTypes</em>.</p>
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235 </dd>
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236 <dt><strong><strong>-a, --AtomIdentifierType</strong> <em>AtomicInvariantsAtomTypes | DREIDINGAtomTypes | EStateAtomTypes | FunctionalClassAtomTypes | MMFF94AtomTypes | SLogPAtomTypes | SYBYLAtomTypes | TPSAAtomTypes | UFFAtomTypes</em></strong></dt>
|
|
237 <dd>
|
|
238 <p>Specify atom identifier type to use during generation of atom path strings
|
|
239 corresponding to path length fingerprints. Possible values in the current release are:
|
|
240 <em>AtomicInvariantsAtomTypes, DREIDINGAtomTypes, EStateAtomTypes,
|
|
241 FunctionalClassAtomTypes, MMFF94AtomTypes, SLogPAtomTypes, SYBYLAtomTypes,
|
|
242 TPSAAtomTypes, UFFAtomTypes</em>. Default value: <em>AtomicInvariantsAtomTypes</em>.</p>
|
|
243 </dd>
|
|
244 <dt><strong><strong>--AtomicInvariantsToUse</strong> <em>"AtomicInvariant1,AtomicInvariant2..."</em></strong></dt>
|
|
245 <dd>
|
|
246 <p>This value is used during <em>AtomicInvariantsAtomTypes</em> value of <strong>a, --AtomIdentifierType</strong>
|
|
247 option. It's a list of comma separated valid atomic invariant atom types.</p>
|
|
248 <p>Possible values for atomic invariants are: <em>AS, X, BO, LBO, SB, DB, TB,
|
|
249 H, Ar, RA, FC, MN, SM</em>. Default value: <em>AS</em>.</p>
|
|
250 <p>The atomic invariants abbreviations correspond to:</p>
|
|
251 <div class="OptionsBox">
|
|
252 AS = Atom symbol corresponding to element symbol</div>
|
|
253 <div class="OptionsBox">
|
|
254 X<n> = Number of non-hydrogen atom neighbors or heavy atoms
|
|
255 <br/> BO<n> = Sum of bond orders to non-hydrogen atom neighbors or heavy atoms
|
|
256 <br/> LBO<n> = Largest bond order of non-hydrogen atom neighbors or heavy atoms
|
|
257 <br/> SB<n> = Number of single bonds to non-hydrogen atom neighbors or heavy atoms
|
|
258 <br/> DB<n> = Number of double bonds to non-hydrogen atom neighbors or heavy atoms
|
|
259 <br/> TB<n> = Number of triple bonds to non-hydrogen atom neighbors or heavy atoms
|
|
260 <br/> H<n> = Number of implicit and explicit hydrogens for atom
|
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261 <br/> Ar = Aromatic annotation indicating whether atom is aromatic
|
|
262 <br/> RA = Ring atom annotation indicating whether atom is a ring
|
|
263 <br/> FC<+n/-n> = Formal charge assigned to atom
|
|
264 <br/> MN<n> = Mass number indicating isotope other than most abundant isotope
|
|
265 <br/> SM<n> = Spin multiplicity of atom. Possible values: 1 (singlet), 2 (doublet) or
|
|
266 3 (triplet)</div>
|
|
267 <p>Atom type generated by AtomTypes::AtomicInvariantsAtomTypes class corresponds to:</p>
|
|
268 <div class="OptionsBox">
|
|
269 AS.X<n>.BO<n>.LBO<n>.<SB><n>.<DB><n>.<TB><n>.H<n>.Ar.RA.FC<+n/-n>.MN<n>.SM<n></div>
|
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270 <p>Except for AS which is a required atomic invariant in atom types, all other atomic invariants are
|
|
271 optional. Atom type specification doesn't include atomic invariants with zero or undefined values.</p>
|
|
272 <p>In addition to usage of abbreviations for specifying atomic invariants, the following descriptive words
|
|
273 are also allowed:</p>
|
|
274 <div class="OptionsBox">
|
|
275 X : NumOfNonHydrogenAtomNeighbors or NumOfHeavyAtomNeighbors
|
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276 <br/> BO : SumOfBondOrdersToNonHydrogenAtoms or SumOfBondOrdersToHeavyAtoms
|
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277 <br/> LBO : LargestBondOrderToNonHydrogenAtoms or LargestBondOrderToHeavyAtoms
|
|
278 <br/> SB : NumOfSingleBondsToNonHydrogenAtoms or NumOfSingleBondsToHeavyAtoms
|
|
279 <br/> DB : NumOfDoubleBondsToNonHydrogenAtoms or NumOfDoubleBondsToHeavyAtoms
|
|
280 <br/> TB : NumOfTripleBondsToNonHydrogenAtoms or NumOfTripleBondsToHeavyAtoms
|
|
281 <br/> H : NumOfImplicitAndExplicitHydrogens
|
|
282 <br/> Ar : Aromatic
|
|
283 <br/> RA : RingAtom
|
|
284 <br/> FC : FormalCharge
|
|
285 <br/> MN : MassNumber
|
|
286 <br/> SM : SpinMultiplicity</div>
|
|
287 <p>Examples:</p>
|
|
288 <p><strong>Benzene</strong>: Using value of <em>AS</em> for <strong>--AtomicInvariantsToUse</strong>, <em>Yes</em> for <strong>UseBondSymbols</strong>,
|
|
289 and <em> AllAtomPathsWithRings</em> for <strong>-p, --PathMode</strong>, atom path strings generated are:</p>
|
|
290 <div class="OptionsBox">
|
|
291 C C:C C:C:C C:C:C:C C:C:C:C:C C:C:C:C:C:C C:C:C:C:C:C:C</div>
|
|
292 <p>And using <em>AS,X,BO</em> for <strong>--AtomicInvariantsToUse</strong> generates following atom path
|
|
293 strings:</p>
|
|
294 <div class="OptionsBox">
|
|
295 C.X2.BO3 C.X2.BO3:C.X2.BO3 C.X2.BO3:C.X2.BO3:C.X2.BO3
|
|
296 <br/> C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3
|
|
297 <br/> C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3
|
|
298 <br/> C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3
|
|
299 <br/> C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3:C.X2.BO3</div>
|
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300 <p><strong>Urea</strong>: Using value of <em>AS</em> for <strong>--AtomicInvariantsToUse</strong>, <em>Yes</em> for <strong>UseBondSymbols</strong>,
|
|
301 and <em> AllAtomPathsWithRings</em> for <strong>-p, --PathMode</strong>, atom path strings are:</p>
|
|
302 <div class="OptionsBox">
|
|
303 C N O C=O CN NC=O NCN</div>
|
|
304 <p>And using <em>AS,X,BO</em> for <strong>--AtomicInvariantsToUse</strong> generates following atom path
|
|
305 strings:</p>
|
|
306 <div class="OptionsBox">
|
|
307 C.X3.BO4 N.X1.BO1 O.X1.BO2 C.X3.BO4=O.X1.BO2
|
|
308 <br/> C.X3.BO4N.X1.BO1 N.X1.BO1C.X3.BO4=O.X1.BO2
|
|
309 <br/> N.X1.BO1C.X3.BO4N.X1.BO1</div>
|
|
310 </dd>
|
|
311 <dt><strong><strong>--FunctionalClassesToUse</strong> <em>"FunctionalClass1,FunctionalClass2..."</em></strong></dt>
|
|
312 <dd>
|
|
313 <p>This value is used during <em>FunctionalClassAtomTypes</em> value of <strong>a, --AtomIdentifierType</strong>
|
|
314 option. It's a list of comma separated valid functional classes.</p>
|
|
315 <p>Possible values for atom functional classes are: <em>Ar, CA, H, HBA, HBD, Hal, NI, PI, RA</em>.
|
|
316 Default value [ Ref 24 ]: <em>HBD,HBA,PI,NI,Ar,Hal</em>.</p>
|
|
317 <p>The functional class abbreviations correspond to:</p>
|
|
318 <div class="OptionsBox">
|
|
319 HBD: HydrogenBondDonor
|
|
320 <br/> HBA: HydrogenBondAcceptor
|
|
321 <br/> PI : PositivelyIonizable
|
|
322 <br/> NI : NegativelyIonizable
|
|
323 <br/> Ar : Aromatic
|
|
324 <br/> Hal : Halogen
|
|
325 <br/> H : Hydrophobic
|
|
326 <br/> RA : RingAtom
|
|
327 <br/> CA : ChainAtom</div>
|
|
328 <div class="OptionsBox">
|
|
329 Functional class atom type specification for an atom corresponds to:</div>
|
|
330 <div class="OptionsBox">
|
|
331 Ar.CA.H.HBA.HBD.Hal.NI.PI.RA</div>
|
|
332 <p><em>AtomTypes::FunctionalClassAtomTypes</em> module is used to assign functional class atom
|
|
333 types. It uses following definitions [ Ref 60-61, Ref 65-66 ]:</p>
|
|
334 <div class="OptionsBox">
|
|
335 HydrogenBondDonor: NH, NH2, OH
|
|
336 <br/> HydrogenBondAcceptor: N[!H], O
|
|
337 <br/> PositivelyIonizable: +, NH2
|
|
338 <br/> NegativelyIonizable: -, C(=O)OH, S(=O)OH, P(=O)OH</div>
|
|
339 </dd>
|
|
340 <dt><strong><strong>--BitsOrder</strong> <em>Ascending | Descending</em></strong></dt>
|
|
341 <dd>
|
|
342 <p>Bits order to use during generation of fingerprints bit-vector string for <em>PathLengthBits</em> value of
|
|
343 <strong>-m, --mode</strong> option. Possible values: <em>Ascending, Descending</em>. Default: <em>Ascending</em>.</p>
|
|
344 <p><em>Ascending</em> bit order which corresponds to first bit in each byte as the lowest bit as
|
|
345 opposed to the highest bit.</p>
|
|
346 <p>Internally, bits are stored in <em>Ascending</em> order using Perl vec function. Regardless
|
|
347 of machine order, big-endian or little-endian, vec function always considers first
|
|
348 string byte as the lowest byte and first bit within each byte as the lowest bit.</p>
|
|
349 </dd>
|
|
350 <dt><strong><strong>-b, --BitStringFormat</strong> <em>BinaryString | HexadecimalString</em></strong></dt>
|
|
351 <dd>
|
|
352 <p>Format of fingerprints bit-vector string data in output SD, FP or CSV/TSV text file(s) specified by
|
|
353 <strong>--output</strong> used during <em>PathLengthBits</em> value of <strong>-m, --mode</strong> option. Possible
|
|
354 values: <em>BinaryString, HexadecimalString</em>. Default value: <em>HexadecimalString</em>.</p>
|
|
355 <p><em>BinaryString</em> corresponds to an ASCII string containing 1s and 0s. <em>HexadecimalString</em>
|
|
356 contains bit values in ASCII hexadecimal format.</p>
|
|
357 <p>Examples:</p>
|
|
358 <div class="OptionsBox">
|
|
359 FingerprintsBitVector;PathLengthBits:AtomicInvariantsAtomTypes:MinLeng
|
|
360 <br/> th1:MaxLength8;1024;BinaryString;Ascending;001000010011010101011000110
|
|
361 <br/> 0100010101011000101001011100110001000010001001101000001001001001001000
|
|
362 <br/> 0010110100000111001001000001001010100100100000000011000000101001011100
|
|
363 <br/> 0010000001000101010100000100111100110111011011011000000010110111001101
|
|
364 <br/> 0101100011000000010001000011000010100011101100001000001000100000000...</div>
|
|
365 <div class="OptionsBox">
|
|
366 FingerprintsBitVector;PathLengthBits:AtomicInvariantsAtomTypes:MinLeng
|
|
367 <br/> th1:MaxLength8;1024;HexadecimalString;Ascending;48caa1315d82d91122b029
|
|
368 <br/> 42861c9409a4208182d12015509767bd0867653604481a8b1288000056090583603078
|
|
369 <br/> 9cedae54e26596889ab121309800900490515224208421502120a0dd9200509723ae89
|
|
370 <br/> 00024181b86c0122821d4e4880c38620dab280824b455404009f082003d52c212b4e6d
|
|
371 <br/> 6ea05280140069c780290c43</div>
|
|
372 </dd>
|
|
373 <dt><strong><strong>--CompoundID</strong> <em>DataFieldName or LabelPrefixString</em></strong></dt>
|
|
374 <dd>
|
|
375 <p>This value is <strong>--CompoundIDMode</strong> specific and indicates how compound ID is generated.</p>
|
|
376 <p>For <em>DataField</em> value of <strong>--CompoundIDMode</strong> option, it corresponds to datafield label name
|
|
377 whose value is used as compound ID; otherwise, it's a prefix string used for generating compound
|
|
378 IDs like LabelPrefixString<Number>. Default value, <em>Cmpd</em>, generates compound IDs which
|
|
379 look like Cmpd<Number>.</p>
|
|
380 <p>Examples for <em>DataField</em> value of <strong>--CompoundIDMode</strong>:</p>
|
|
381 <div class="OptionsBox">
|
|
382 MolID
|
|
383 <br/> ExtReg</div>
|
|
384 <p>Examples for <em>LabelPrefix</em> or <em>MolNameOrLabelPrefix</em> value of <strong>--CompoundIDMode</strong>:</p>
|
|
385 <div class="OptionsBox">
|
|
386 Compound</div>
|
|
387 <p>The value specified above generates compound IDs which correspond to Compound<Number>
|
|
388 instead of default value of Cmpd<Number>.</p>
|
|
389 </dd>
|
|
390 <dt><strong><strong>--CompoundIDLabel</strong> <em>text</em></strong></dt>
|
|
391 <dd>
|
|
392 <p>Specify compound ID column label for FP or CSV/TSV text file(s) used during <em>CompoundID</em> value
|
|
393 of <strong>--DataFieldsMode</strong> option. Default: <em>CompoundID</em>.</p>
|
|
394 </dd>
|
|
395 <dt><strong><strong>--CompoundIDMode</strong> <em>DataField | MolName | LabelPrefix | MolNameOrLabelPrefix</em></strong></dt>
|
|
396 <dd>
|
|
397 <p>Specify how to generate compound IDs and write to FP or CSV/TSV text file(s) along with generated
|
|
398 fingerprints for <em>FP | text | all</em> values of <strong>--output</strong> option: use a <em>SDFile(s)</em> datafield value;
|
|
399 use molname line from <em>SDFile(s)</em>; generate a sequential ID with specific prefix; use combination
|
|
400 of both MolName and LabelPrefix with usage of LabelPrefix values for empty molname lines.</p>
|
|
401 <p>Possible values: <em>DataField | MolName | LabelPrefix | MolNameOrLabelPrefix</em>.
|
|
402 Default: <em>LabelPrefix</em>.</p>
|
|
403 <p>For <em>MolNameAndLabelPrefix</em> value of <strong>--CompoundIDMode</strong>, molname line in <em>SDFile(s)</em> takes
|
|
404 precedence over sequential compound IDs generated using <em>LabelPrefix</em> and only empty molname
|
|
405 values are replaced with sequential compound IDs.</p>
|
|
406 <p>This is only used for <em>CompoundID</em> value of <strong>--DataFieldsMode</strong> option.</p>
|
|
407 </dd>
|
|
408 <dt><strong><strong>--DataFields</strong> <em>"FieldLabel1,FieldLabel2,... "</em></strong></dt>
|
|
409 <dd>
|
|
410 <p>Comma delimited list of <em>SDFiles(s)</em> data fields to extract and write to CSV/TSV text file(s) along
|
|
411 with generated fingerprints for <em>text | all</em> values of <strong>--output</strong> option.</p>
|
|
412 <p>This is only used for <em>Specify</em> value of <strong>--DataFieldsMode</strong> option.</p>
|
|
413 <p>Examples:</p>
|
|
414 <div class="OptionsBox">
|
|
415 Extreg
|
|
416 <br/> MolID,CompoundName</div>
|
|
417 </dd>
|
|
418 <dt><strong><strong>-d, --DataFieldsMode</strong> <em>All | Common | Specify | CompoundID</em></strong></dt>
|
|
419 <dd>
|
|
420 <p>Specify how data fields in <em>SDFile(s)</em> are transferred to output CSV/TSV text file(s) along
|
|
421 with generated fingerprints for <em>text | all</em> values of <strong>--output</strong> option: transfer all SD
|
|
422 data field; transfer SD data files common to all compounds; extract specified data fields;
|
|
423 generate a compound ID using molname line, a compound prefix, or a combination of both.
|
|
424 Possible values: <em>All | Common | specify | CompoundID</em>. Default value: <em>CompoundID</em>.</p>
|
|
425 </dd>
|
|
426 <dt><strong><strong>--DetectAromaticity</strong> <em>Yes | No</em></strong></dt>
|
|
427 <dd>
|
|
428 <p>Detect aromaticity before generating fingerprints. Possible values: <em>Yes or No</em>.
|
|
429 Default value: <em>Yes</em>.</p>
|
|
430 <p><em>No</em> <strong>--DetectAromaticity</strong> forces usage of atom and bond aromaticity values
|
|
431 from <em>SDFile(s)</em> and skips the step which detects and assigns aromaticity.</p>
|
|
432 <p><em>No</em> <strong>--DetectAromaticity</strong> value is only allowed uring <em>AtomicInvariantsAtomTypes</em>
|
|
433 value of <strong>-a, --AtomIdentifierType</strong> options; for all possible values <strong>-a, --AtomIdentifierType</strong>
|
|
434 values, it must be <em>Yes</em>.</p>
|
|
435 </dd>
|
|
436 <dt><strong><strong>-f, --Filter</strong> <em>Yes | No</em></strong></dt>
|
|
437 <dd>
|
|
438 <p>Specify whether to check and filter compound data in SDFile(s). Possible values: <em>Yes or No</em>.
|
|
439 Default value: <em>Yes</em>.</p>
|
|
440 <p>By default, compound data is checked before calculating fingerprints and compounds containing
|
|
441 atom data corresponding to non-element symbols or no atom data are ignored.</p>
|
|
442 </dd>
|
|
443 <dt><strong><strong>--FingerprintsLabel</strong> <em>text</em></strong></dt>
|
|
444 <dd>
|
|
445 <p>SD data label or text file column label to use for fingerprints string in output SD or
|
|
446 CSV/TSV text file(s) specified by <strong>--output</strong>. Default value: <em>PathLenghFingerprints</em>.</p>
|
|
447 </dd>
|
|
448 <dt><strong><strong>--fold</strong> <em>Yes | No</em></strong></dt>
|
|
449 <dd>
|
|
450 <p>Fold fingerprints to increase bit density during <em>PathLengthBits</em> value of
|
|
451 <strong>-m, --mode</strong> option. Possible values: <em>Yes or No</em>. Default value: <em>No</em>.</p>
|
|
452 </dd>
|
|
453 <dt><strong><strong>--FoldedSize</strong> <em>number</em></strong></dt>
|
|
454 <dd>
|
|
455 <p>Size of folded fingerprint during <em>PathLengthBits</em> value of <strong>-m, --mode</strong> option. Default
|
|
456 value: <em>256</em>. Valid values correspond to any positive integer which is less than
|
|
457 <strong>-s, --size</strong> and meets the criteria for its value.</p>
|
|
458 <p>Examples:</p>
|
|
459 <div class="OptionsBox">
|
|
460 128
|
|
461 512</div>
|
|
462 </dd>
|
|
463 <dt><strong><strong>-h, --help</strong></strong></dt>
|
|
464 <dd>
|
|
465 <p>Print this help message</p>
|
|
466 </dd>
|
|
467 <dt><strong><strong>-i, --IgnoreHydrogens</strong> <em>Yes | No</em></strong></dt>
|
|
468 <dd>
|
|
469 <p>Ignore hydrogens during fingerprints generation. Possible values: <em>Yes or No</em>.
|
|
470 Default value: <em>Yes</em>.</p>
|
|
471 <p>For <em>yes</em> value of <strong>-i, --IgnoreHydrogens</strong>, any explicit hydrogens are also used for
|
|
472 generation of atoms path lengths and fingerprints; implicit hydrogens are still ignored.</p>
|
|
473 </dd>
|
|
474 <dt><strong><strong>-k, --KeepLargestComponent</strong> <em>Yes | No</em></strong></dt>
|
|
475 <dd>
|
|
476 <p>Generate fingerprints for only the largest component in molecule. Possible values:
|
|
477 <em>Yes or No</em>. Default value: <em>Yes</em>.</p>
|
|
478 <p>For molecules containing multiple connected components, fingerprints can be generated
|
|
479 in two different ways: use all connected components or just the largest connected
|
|
480 component. By default, all atoms except for the largest connected component are
|
|
481 deleted before generation of fingerprints.</p>
|
|
482 </dd>
|
|
483 <dt><strong><strong>-m, --mode</strong> <em>PathLengthBits | PathLengthCount</em></strong></dt>
|
|
484 <dd>
|
|
485 <p>Specify type of path length fingerprints to generate for molecules in <em>SDFile(s)</em>. Possible
|
|
486 values: <em>PathLengthBits, PathLengthCount</em>. Default value: <em>PathLengthBits</em>.</p>
|
|
487 <p>For <em>PathLengthBits</em> value of <strong>-m, --mode</strong> option, a fingerprint bit-vector string containing
|
|
488 zeros and ones is generated and for <em>PathLengthCount</em> value, a fingerprint vector string
|
|
489 corresponding to number of atom paths is generated.</p>
|
|
490 </dd>
|
|
491 <dt><strong><strong>--MinPathLength</strong> <em>number</em></strong></dt>
|
|
492 <dd>
|
|
493 <p>Minimum atom path length to include in fingerprints. Default value: <em>1</em>. Valid values:
|
|
494 positive integers and less than <strong>--MaxPathLength</strong>. Path length of 1 correspond to
|
|
495 a path containing only one atom.</p>
|
|
496 </dd>
|
|
497 <dt><strong><strong>--MaxPathLength</strong> <em>number</em></strong></dt>
|
|
498 <dd>
|
|
499 <p>Maximum atom path length to include in fingerprints. Default value: <em>8</em>. Valid values:
|
|
500 positive integers and greater than <strong>--MinPathLength</strong>.</p>
|
|
501 </dd>
|
|
502 <dt><strong><strong>-n, --NumOfBitsToSetPerPath</strong> <em>number</em></strong></dt>
|
|
503 <dd>
|
|
504 <p>Number of bits to set per path during generation of fingerprints bit-vector string for <em>PathLengthBits</em>
|
|
505 value of <strong>-m, --mode</strong> option. Default value: <em>1</em>. Valid values: positive integers.</p>
|
|
506 </dd>
|
|
507 <dt><strong><strong>--OutDelim</strong> <em>comma | tab | semicolon</em></strong></dt>
|
|
508 <dd>
|
|
509 <p>Delimiter for output CSV/TSV text file(s). Possible values: <em>comma, tab, or semicolon</em>
|
|
510 Default value: <em>comma</em>.</p>
|
|
511 </dd>
|
|
512 <dt><strong><strong>--output</strong> <em>SD | FP | text | all</em></strong></dt>
|
|
513 <dd>
|
|
514 <p>Type of output files to generate. Possible values: <em>SD, FP, text, or all</em>. Default value: <em>text</em>.</p>
|
|
515 </dd>
|
|
516 <dt><strong><strong>-o, --overwrite</strong></strong></dt>
|
|
517 <dd>
|
|
518 <p>Overwrite existing files.</p>
|
|
519 </dd>
|
|
520 <dt><strong><strong>-p, --PathMode</strong> <em>AtomPathsWithoutRings | AtomPathsWithRings | AllAtomPathsWithoutRings | AllAtomPathsWithRings</em></strong></dt>
|
|
521 <dd>
|
|
522 <p>Specify type of atom paths to use for generating pathlength fingerprints for molecules in
|
|
523 <em>SDFile(s)</em>. Possible values:<em>AtomPathsWithoutRings, AtomPathsWithRings,
|
|
524 AllAtomPathsWithoutRings, AllAtomPathsWithRings</em>. Default value: <em>AllAtomPathsWithRings</em>.</p>
|
|
525 <p>For molecules with no rings, first two and last two options are equivalent and generate
|
|
526 same set of atom paths starting from each atom with length between <strong>--MinPathLength</strong>
|
|
527 and <strong>--MaxPathLength</strong>. However, all these four options can result in the same set of
|
|
528 final atom paths for molecules containing fused, bridged or spiro rings.</p>
|
|
529 <p>For molecules containing rings, atom paths starting from each atom can be traversed in
|
|
530 four different ways:</p>
|
|
531 <p><em>AtomPathsWithoutRings</em> - Atom paths containing no rings and without sharing of bonds
|
|
532 in traversed paths.</p>
|
|
533 <p><em>AtomPathsWithRings</em> - Atom paths containing rings and without any sharing of bonds in
|
|
534 traversed paths.</p>
|
|
535 <p><em>AllAtomPathsWithoutRings</em> - All possible atom paths containing no rings and without any
|
|
536 sharing of bonds in traversed paths.</p>
|
|
537 <p><em>AllAtomPathsWithRings</em> - All possible atom paths containing rings and with sharing of
|
|
538 bonds in traversed paths.</p>
|
|
539 <p>Atom path traversal is terminated at the ring atom.</p>
|
|
540 <p>Based on values specified for for <strong>-p, --PathMode</strong>, <strong>--MinPathLength</strong> and
|
|
541 <strong>--MaxPathLength</strong>, all appropriate atom paths are generated for each atom in the molecule
|
|
542 and collected in a list.</p>
|
|
543 <p>For each atom path in the filtered atom paths list, an atom path string is created using value of
|
|
544 <strong>-a, --AtomIdentifierType</strong> and specified values to use for a particular atom identifier type.
|
|
545 Value of <strong>-u, --UseBondSymbols</strong> controls whether bond order symbols are used during generation
|
|
546 of atom path string. Atom symbol corresponds to element symbol and characters used to represent
|
|
547 bond order are: <em>1 - None; 2 - '='; 3 - '#'; 1.5 or aromatic - ':'; others: bond order value</em>. By default,
|
|
548 bond symbols are included in atom path strings. Exclusion of bond symbols in atom path strings
|
|
549 results in fingerprints which correspond purely to atom paths without considering bonds.</p>
|
|
550 <p><strong>UseUniquePaths</strong> controls the removal of structurally duplicate atom path strings are removed
|
|
551 from the list.</p>
|
|
552 <p>For <em>PathLengthBits</em> value of <strong>-m, --mode</strong> option, each atom path is hashed to a 32 bit unsigned
|
|
553 integer key using <strong>TextUtil::HashCode</strong> function. Using the hash key as a seed for a random number
|
|
554 generator, a random integer value between 0 and <strong>--Size</strong> is used to set corresponding bits
|
|
555 in the fingerprint bit-vector string. Value of <strong>--NumOfBitsToSetPerPaths</strong> option controls the number
|
|
556 of time a random number is generated to set corresponding bits.</p>
|
|
557 <p>For <em> PathLengthCount</em> value of <strong>-m, --mode</strong> option, the number of times an atom path appears
|
|
558 is tracked and a fingerprints count-string corresponding to count of atom paths is generated.</p>
|
|
559 <p>For molecule containing rings, combination of <strong>-p, --PathMode</strong> and <strong>--UseBondSymbols</strong> allows
|
|
560 generation of up to 8 different types of atom path length strings:</p>
|
|
561 <div class="OptionsBox">
|
|
562 AllowSharedBonds AllowRings UseBondSymbols</div>
|
|
563 <div class="OptionsBox">
|
|
564 0 0 1 - AtomPathsNoCyclesWithBondSymbols
|
|
565 <br/> 0 1 1 - AtomPathsWithCyclesWithBondSymbols</div>
|
|
566 <div class="OptionsBox">
|
|
567 1 0 1 - AllAtomPathsNoCyclesWithBondSymbols
|
|
568 <br/> 1 1 1 - AllAtomPathsWithCyclesWithBondSymbols
|
|
569 [ DEFAULT ]</div>
|
|
570 <div class="OptionsBox">
|
|
571 0 0 0 - AtomPathsNoCyclesNoBondSymbols
|
|
572 <br/> 0 1 0 - AtomPathsWithCyclesNoBondSymbols</div>
|
|
573 <div class="OptionsBox">
|
|
574 1 0 0 - AllAtomPathsNoCyclesNoBondSymbols
|
|
575 <br/> 1 1 0 - AllAtomPathsWithCyclesNoWithBondSymbols</div>
|
|
576 <p>Default atom path length fingerprints generation for molecules containing rings with
|
|
577 <em>AllAtomPathsWithRings</em> value for <strong>-p, --PathMode</strong>, <em>Yes</em> value for <strong>--UseBondSymbols</strong>,
|
|
578 <em>2</em> value for <strong>--MinPathLength</strong> and <em>8</em> value for <strong>--MaxPathLength</strong> is the most time
|
|
579 consuming. Combinations of other options can substantially speed up fingerprint generation
|
|
580 for molecules containing complex ring systems.</p>
|
|
581 <p>Additionally, value for option <strong>-a, --AtomIdentifierType</strong> in conjunction with corresponding specified
|
|
582 values for atom types changes the nature of atom path length strings and the fingerprints.</p>
|
|
583 </dd>
|
|
584 <dt><strong><strong>-q, --quote</strong> <em>Yes | No</em></strong></dt>
|
|
585 <dd>
|
|
586 <p>Put quote around column values in output CSV/TSV text file(s). Possible values:
|
|
587 <em>Yes or No</em>. Default value: <em>Yes</em>.</p>
|
|
588 </dd>
|
|
589 <dt><strong><strong>-r, --root</strong> <em>RootName</em></strong></dt>
|
|
590 <dd>
|
|
591 <p>New file name is generated using the root: <Root>.<Ext>. Default for new file
|
|
592 names: <SDFileName><PathLengthFP>.<Ext>. The file type determines <Ext> value.
|
|
593 The sdf, fpf, csv, and tsv <Ext> values are used for SD, FP, comma/semicolon, and tab
|
|
594 delimited text files, respectively.This option is ignored for multiple input files.</p>
|
|
595 </dd>
|
|
596 <dt><strong><strong>-s, --size</strong> <em>number</em></strong></dt>
|
|
597 <dd>
|
|
598 <p>Size of fingerprints. Default value: <em>1024</em>. Valid values correspond to any positive
|
|
599 integer which satisfies the following criteria: power of 2, >= 32 and <= 2 ** 32.</p>
|
|
600 <p>Examples:</p>
|
|
601 <div class="OptionsBox">
|
|
602 256
|
|
603 512
|
|
604 2048</div>
|
|
605 </dd>
|
|
606 <dt><strong><strong>-u, --UseBondSymbols</strong> <em>Yes | No</em></strong></dt>
|
|
607 <dd>
|
|
608 <p>Specify whether to use bond symbols for atom paths during generation of atom path strings.
|
|
609 Possible values: <em>Yes or No</em>. Default value: <em>Yes</em>.</p>
|
|
610 <p><em>No</em> value option for <strong>-u, --UseBondSymbols</strong> allows the generation of fingerprints corresponding
|
|
611 purely to atoms disregarding all bonds.</p>
|
|
612 </dd>
|
|
613 <dt><strong><strong>--UsePerlCoreRandom</strong> <em>Yes | No</em></strong></dt>
|
|
614 <dd>
|
|
615 <p>Specify whether to use Perl CORE::rand or MayaChemTools MathUtil::random function
|
|
616 during random number generation for setting bits in fingerprints bit-vector strings. Possible
|
|
617 values: <em>Yes or No</em>. Default value: <em>Yes</em>.</p>
|
|
618 <p><em>No</em> value option for <strong>--UsePerlCoreRandom</strong> allows the generation of fingerprints
|
|
619 bit-vector strings which are same across different platforms.</p>
|
|
620 <p>The random number generator implemented in MayaChemTools is a variant of
|
|
621 linear congruential generator (LCG) as described by Miller et al. [ Ref 120 ].
|
|
622 It is also referred to as Lehmer random number generator or Park-Miller
|
|
623 random number generator.</p>
|
|
624 <p>Unlike Perl's core random number generator function rand, the random number
|
|
625 generator implemented in MayaChemTools, MathUtil::random, generates consistent
|
|
626 random values across different platforms for a specific random seed and leads
|
|
627 to generation of portable fingerprints bit-vector strings.</p>
|
|
628 </dd>
|
|
629 <dt><strong><strong>--UseUniquePaths</strong> <em>Yes | No</em></strong></dt>
|
|
630 <dd>
|
|
631 <p>Specify whether to use structurally unique atom paths during generation of atom path strings.
|
|
632 Possible values: <em>Yes or No</em>. Default value: <em>Yes</em>.</p>
|
|
633 <p><em>No</em> value option for <strong>--UseUniquePaths</strong> allows usage of all atom paths generated by
|
|
634 <strong>-p, --PathMode</strong> option value for generation of atom path strings leading to duplicate
|
|
635 path count during <em>PathLengthCount</em> value of <strong>-m, --mode</strong> option. It doesn't change fingerprint
|
|
636 string generated during <em>PathLengthBits</em> value of <strong>-m, --mode</strong>.</p>
|
|
637 <p>For example, during <em>AllAtomPathsWithRings</em> value of <strong>-p, --PathMode</strong> option, benzene has
|
|
638 12 linear paths of length 2 and 12 cyclic paths length of 7, but only 6 linear paths of length 2 and
|
|
639 1 cyclic path of length 7 are structurally unique.</p>
|
|
640 </dd>
|
|
641 <dt><strong><strong>-v, --VectorStringFormat</strong> <em>IDsAndValuesString | IDsAndValuesPairsString | ValuesAndIDsString | ValuesAndIDsPairsString</em></strong></dt>
|
|
642 <dd>
|
|
643 <p>Format of fingerprints vector string data in output SD, FP or CSV/TSV text file(s) specified by
|
|
644 <strong>--output</strong> used during <em>PathLengthCount</em> value of <strong>-m, --mode</strong> option. Possible
|
|
645 values: <em>IDsAndValuesString | IDsAndValuesPairsString | ValuesAndIDsString |
|
|
646 ValuesAndIDsPairsString</em>. Defaultvalue: <em>IDsAndValuesString</em>.</p>
|
|
647 <p>Examples:</p>
|
|
648 <div class="OptionsBox">
|
|
649 FingerprintsVector;PathLengthCount:AtomicInvariantsAtomTypes:MinLength
|
|
650 <br/> 1:MaxLength8;432;NumericalValues;IDsAndValuesPairsString;C.X1.BO1.H3 2
|
|
651 C.X2.BO2.H2 4 C.X2.BO3.H1 14 C.X3.BO3.H1 3 C.X3.BO4 10 F.X1.BO1 1 N.X
|
|
652 <br/> 2.BO2.H1 1 N.X3.BO3 1 O.X1.BO1.H1 3 O.X1.BO2 2 C.X1.BO1.H3C.X3.BO3.H1
|
|
653 <br/> 2 C.X2.BO2.H2C.X2.BO2.H2 1 C.X2.BO2.H2C.X3.BO3.H1 4 C.X2.BO2.H2C.X3.BO
|
|
654 <br/> 4 1 C.X2.BO2.H2N.X3.BO3 1 C.X2.BO3.H1:C.X2.BO3.H1 10 C.X2.BO3.H1:C....</div>
|
|
655 <div class="OptionsBox">
|
|
656 FingerprintsVector;PathLengthCount:EStateAtomTypes:MinLength1:MaxLengt
|
|
657 <br/> h8;454;NumericalValues;IDsAndValuesPairsString;aaCH 14 aasC 8 aasN 1 d
|
|
658 <br/> O 2 dssC 2 sCH3 2 sF 1 sOH 3 ssCH2 4 ssNH 1 sssCH 3 aaCH:aaCH 10 aaCH:
|
|
659 <br/> aasC 8 aasC:aasC 3 aasC:aasN 2 aasCaasC 2 aasCdssC 1 aasCsF 1 aasCssNH
|
|
660 <br/> 1 aasCsssCH 1 aasNssCH2 1 dO=dssC 2 dssCsOH 1 dssCssCH2 1 dssCssNH 1
|
|
661 <br/> sCH3sssCH 2 sOHsssCH 2 ssCH2ssCH2 1 ssCH2sssCH 4 aaCH:aaCH:aaCH 6 a...</div>
|
|
662 </dd>
|
|
663 <dt><strong><strong>-w, --WorkingDir</strong> <em>DirName</em></strong></dt>
|
|
664 <dd>
|
|
665 <p>Location of working directory. Default: current directory.</p>
|
|
666 </dd>
|
|
667 </dl>
|
|
668 <p>
|
|
669 </p>
|
|
670 <h2>EXAMPLES</h2>
|
|
671 <p>To generate path length fingerprints corresponding to all unique paths from length 1
|
|
672 through 8 in hexadecimal bit-vector string format of size 1024 and create a
|
|
673 SamplePLFPHex.csv file containing sequential compound IDs along with fingerprints
|
|
674 bit-vector strings data, type:</p>
|
|
675 <div class="ExampleBox">
|
|
676 % PathLengthFingerprints.pl -o -r SamplePLFPHex Sample.sdf</div>
|
|
677 <p>To generate path length fingerprints corresponding to all unique paths from length 1
|
|
678 through 8 in hexadecimal bit-vector string format of size 1024 and create SamplePLFPHex.sdf,
|
|
679 SamplePLFPHex.fpf, and SamplePLFPHex.csv files containing sequential compound IDs
|
|
680 in CSV file along with fingerprints bit-vector strings data, type:</p>
|
|
681 <div class="ExampleBox">
|
|
682 % PathLengthFingerprints.pl --output all -o -r SamplePLFPHex Sample.sdf</div>
|
|
683 <p>To generate path length fingerprints corresponding to all unique paths from length 1
|
|
684 through 8 in binary bit-vector string format of size 1024 and create a
|
|
685 SamplePLFPBin.csv file containing sequential compound IDs along with fingerprints
|
|
686 bit-vector strings data, type:</p>
|
|
687 <div class="ExampleBox">
|
|
688 % PathLengthFingerprints.pl --BitStringFormat BinaryString --size 2048
|
|
689 -o -r SamplePLFPBin Sample.sdf</div>
|
|
690 <p>To generate path length fingerprints corresponding to count of all unique paths from
|
|
691 length 1 through 8 in IDsAndValuesString format and create a SamplePLFPCount.csv file
|
|
692 containing sequential compound IDs along with fingerprints vector strings data, type:</p>
|
|
693 <div class="ExampleBox">
|
|
694 % PathLengthFingerprints.pl -m PathLengthCount -o -r SamplePLFPCount
|
|
695 Sample.sdf</div>
|
|
696 <p>To generate path length fingerprints corresponding to count of all unique paths from
|
|
697 length 1 through 8 in IDsAndValuesString format using E-state atom types and
|
|
698 create a SamplePLFPCount.csv file containing sequential compound IDs along with fingerprints
|
|
699 vector strings data, type:</p>
|
|
700 <div class="ExampleBox">
|
|
701 % PathLengthFingerprints.pl -m PathLengthCount --AtomIdentifierType
|
|
702 EStateAtomTypes -o -r SamplePLFPCount Sample.sdf</div>
|
|
703 <p>To generate path length fingerprints corresponding to count of all unique paths from
|
|
704 length 1 through 8 in IDsAndValuesString format using SLogP atom types and
|
|
705 create a SamplePLFPCount.csv file containing sequential compound IDs along with fingerprints
|
|
706 vector strings data, type:</p>
|
|
707 <div class="ExampleBox">
|
|
708 % PathLengthFingerprints.pl -m PathLengthCount --AtomIdentifierType
|
|
709 SLogPAtomTypes -o -r SamplePLFPCount Sample.sdf</div>
|
|
710 <p>To generate path length fingerprints corresponding to count of all unique paths from
|
|
711 length 1 through 8 in IDsAndValuesString format and create a SamplePLFPCount.csv file
|
|
712 containing sequential compound IDs along with fingerprints vector strings data, type:</p>
|
|
713 <div class="ExampleBox">
|
|
714 % PathLengthFingerprints.pl -m PathLengthCount --VectorStringFormat
|
|
715 ValuesAndIDsPairsString -o -r SamplePLFPCount Sample.sdf</div>
|
|
716 <p>To generate path length fingerprints corresponding to count of all unique paths from
|
|
717 length 1 through 8 in IDsAndValuesString format using AS,X,BO as atomic invariants and
|
|
718 create a SamplePLFPCount.csv file containing sequential compound IDs along with fingerprints
|
|
719 vector strings data, type:</p>
|
|
720 <div class="ExampleBox">
|
|
721 % PathLengthFingerprints.pl -m PathLengthCount --AtomIdentifierType
|
|
722 AtomicInvariantsAtomTypes --AtomicInvariantsToUse "AS,X,BO" -o
|
|
723 -r SamplePLFPCount Sample.sdf</div>
|
|
724 <p>To generate path length fingerprints corresponding to count of all paths from
|
|
725 length 1 through 8 in IDsAndValuesString format and create a SamplePLFPCount.csv file
|
|
726 containing compound IDs from MolName line along with fingerprints vector strings data, type:</p>
|
|
727 <div class="ExampleBox">
|
|
728 % PathLengthFingerprints.pl -m PathLengthCount --UseUniquePaths No
|
|
729 -o --CompoundIDMode MolName -r SamplePLFPCount --UseUniquePaths No
|
|
730 Sample.sdf</div>
|
|
731 <p>To generate path length fingerprints corresponding to all unique paths from length 1
|
|
732 through 8 in hexadecimal bit-vector string format of size 512 after folding and create
|
|
733 SamplePLFPHex.sdf, SamplePLFPHex.fpf, and SamplePLFPHex.sdf files containing sequential
|
|
734 compound IDs along with fingerprints bit-vector strings data, type:</p>
|
|
735 <div class="ExampleBox">
|
|
736 % PathLengthFingerprints.pl --output all --Fold Yes --FoldedSize 512
|
|
737 -o -r SamplePLFPHex Sample.sdf</div>
|
|
738 <p>To generate path length fingerprints corresponding to all unique paths from length 1
|
|
739 through 8 containing no rings and without sharing of bonds in hexadecimal bit-vector
|
|
740 string format of size 1024 and create a SamplePLFPHex.csv file containing sequential
|
|
741 compound IDs along with fingerprints bit-vector strings data and all data fields, type:</p>
|
|
742 <div class="ExampleBox">
|
|
743 % PathLengthFingerprints.pl -p AtomPathsWithoutRings --DataFieldsMode All
|
|
744 -o -r SamplePLFPHex Sample.sdf</div>
|
|
745 <p>To generate path length fingerprints corresponding to all unique paths from length 1
|
|
746 through 8 containing rings and without sharing of bonds in hexadecimal bit-vector
|
|
747 string format of size 1024 and create a SamplePLFPHex.tsv file containing compound IDs
|
|
748 derived from combination of molecule name line and an explicit compound prefix
|
|
749 along with fingerprints bit-vector strings data and all data fields, type:</p>
|
|
750 <div class="ExampleBox">
|
|
751 % PathLengthFingerprints.pl -p AtomPathsWithRings --DataFieldsMode
|
|
752 CompoundID --CompoundIDMode MolnameOrLabelPrefix --CompoundID Cmpd
|
|
753 --CompoundIDLabel MolID --FingerprintsLabel PathLengthFP --OutDelim Tab
|
|
754 -r SamplePLFPHex -o Sample.sdf</div>
|
|
755 <p>To generate path length fingerprints corresponding to count of all unique paths from
|
|
756 length 1 through 8 in IDsAndValuesString format and create a SamplePLFPCount.csv file
|
|
757 containing sequential compound IDs along with fingerprints vector strings data using
|
|
758 aromaticity specified in SD file, type:</p>
|
|
759 <div class="ExampleBox">
|
|
760 % PathLengthFingerprints.pl -m PathLengthCount --DetectAromaticity No
|
|
761 -o -r SamplePLFPCount Sample.sdf</div>
|
|
762 <p>To generate path length fingerprints corresponding to all unique paths from length 2
|
|
763 through 6 in hexadecimal bit-vector string format of size 1024 and create a
|
|
764 SamplePLFPHex.csv file containing sequential compound IDs along with fingerprints
|
|
765 bit-vector strings data, type:</p>
|
|
766 <div class="ExampleBox">
|
|
767 % PathLengthFingerprints.pl --MinPathLength 2 --MaxPathLength 6
|
|
768 -o -r SamplePLFPHex Sample.sdf</div>
|
|
769 <p>
|
|
770 </p>
|
|
771 <h2>AUTHOR</h2>
|
|
772 <p><a href="mailto:msud@san.rr.com">Manish Sud</a></p>
|
|
773 <p>
|
|
774 </p>
|
|
775 <h2>SEE ALSO</h2>
|
|
776 <p><a href="./InfoFingerprintsFiles.html">InfoFingerprintsFiles.pl</a>, <a href="./SimilarityMatricesFingerprints.html">SimilarityMatricesFingerprints.pl</a>, <a href="./AtomNeighborhoodsFingerprints.html">AtomNeighborhoodsFingerprints.pl</a>, 
|
|
777 <a href="./ExtendedConnectivityFingerprints.html">ExtendedConnectivityFingerprints.pl</a>, <a href="./MACCSKeysFingerprints.html">MACCSKeysFingerprints.pl</a>, 
|
|
778 <a href="./TopologicalAtomPairsFingerprints.html">TopologicalAtomPairsFingerprints.pl</a>, <a href="./TopologicalAtomTorsionsFingerprints.html">TopologicalAtomTorsionsFingerprints.pl</a>, 
|
|
779 <a href="./TopologicalPharmacophoreAtomPairsFingerprints.html">TopologicalPharmacophoreAtomPairsFingerprints.pl</a>, <a href="./TopologicalPharmacophoreAtomTripletsFingerprints.html">TopologicalPharmacophoreAtomTripletsFingerprints.pl</a>
|
|
780 </p>
|
|
781 <p>
|
|
782 </p>
|
|
783 <h2>COPYRIGHT</h2>
|
|
784 <p>Copyright (C) 2015 Manish Sud. All rights reserved.</p>
|
|
785 <p>This file is part of MayaChemTools.</p>
|
|
786 <p>MayaChemTools is free software; you can redistribute it and/or modify it under
|
|
787 the terms of the GNU Lesser General Public License as published by the Free
|
|
788 Software Foundation; either version 3 of the License, or (at your option)
|
|
789 any later version.</p>
|
|
790 <p> </p><p> </p><div class="DocNav">
|
|
791 <table width="100%" border=0 cellpadding=0 cellspacing=2>
|
|
792 <tr align="left" valign="top"><td width="33%" align="left"><a href="./MolFilesToSD.html" title="MolFilesToSD.html">Previous</a> <a href="./index.html" title="Table of Contents">TOC</a> <a href="./SDFilesToHTML.html" title="SDFilesToHTML.html">Next</a></td><td width="34%" align="middle"><strong>March 29, 2015</strong></td><td width="33%" align="right"><strong>PathLengthFingerprints.pl</strong></td></tr>
|
|
793 </table>
|
|
794 </div>
|
|
795 <br />
|
|
796 <center>
|
|
797 <img src="../../images/h2o2.png">
|
|
798 </center>
|
|
799 </body>
|
|
800 </html>
|