file1
,
file2
, etc. all in the same folder or directory;
first, locate one of the files with the [Browse...] button. Then alter the
file path in the box above to include '*' character (eg. file*
).
Wildcard '?' to blanket only one character works too.Historiographs |
Grand Totals: LCS 21386, GCS 155905, CR 158325 Collection span: 1962 - 1998 | |
Title Word List (4493) Word count: 27039, All words count: 40117 |
# | Word | Recs | TLCS | TGCS |
---|---|---|---|---|
101 | FUNCTION | 40 | 326 | 2107 |
102 | ACID | 62 | 321 | 3338 |
103 | FAST | 27 | 321 | 2183 |
104 | ORIGIN | 12 | 316 | 963 |
105 | BASES | 17 | 309 | 1776 |
106 | UNDERSTANDING | 2 | 305 | 415 |
107 | ROLE | 41 | 303 | 1816 |
108 | CHARACTERIZATION | 66 | 302 | 2652 |
109 | TRANSFER | 97 | 296 | 4704 |
110 | POSSIBLE | 13 | 292 | 763 |
111 | SEVERITY | 13 | 292 | 919 |
112 | HEMOPROTEINS | 38 | 291 | 1611 |
113 | CARBONMONOXY | 20 | 288 | 989 |
114 | TRANSITIONS | 27 | 287 | 1205 |
115 | USING | 51 | 287 | 1628 |
116 | POTASSIUM | 11 | 283 | 592 |
117 | 22 | 282 | 1370 | |
118 | SYSTEM | 30 | 281 | 814 |
119 | FERRICYTOCHROME | 25 | 280 | 1895 |
120 | VIBRATIONAL | 37 | 280 | 2080 |
121 | DEPENDENCE | 41 | 278 | 1503 |
122 | SOLUTION | 57 | 278 | 2578 |
123 | THERAPEUTIC | 10 | 275 | 618 |
124 | INTRACELLULAR | 15 | 272 | 855 |
125 | ACTIVE | 42 | 271 | 2323 |
126 | CARBONMONOXYHEMOGLOBIN | 10 | 271 | 588 |
127 | EVENTS | 17 | 268 | 1386 |
128 | SYNTHESIS | 41 | 267 | 3190 |
129 | HIGH | 57 | 255 | 1890 |
130 | VISCOSITY | 18 | 254 | 721 |
# | Word | Recs | TLCS | TGCS |
131 | MODELS | 46 | 253 | 2833 |
132 | INHIBITION | 28 | 250 | 1061 |
133 | CELLULAR | 11 | 249 | 670 |
134 | HEXACYANOFERRATE | 31 | 249 | 734 |
135 | RAY | 29 | 249 | 1881 |
136 | DETERMINATION | 28 | 247 | 1086 |
137 | PROCESSES | 27 | 247 | 1770 |
138 | DELAY | 8 | 246 | 312 |
139 | REACTIVITY | 18 | 246 | 1074 |
140 | ASPECTS | 14 | 243 | 641 |
141 | COOPERATIVITY | 10 | 242 | 623 |
142 | DETERMINANT | 6 | 242 | 873 |
143 | DEOXYGENATION | 27 | 235 | 575 |
144 | REACTION | 73 | 233 | 2850 |
145 | TERTIARY | 15 | 233 | 959 |
146 | CATION | 30 | 232 | 1066 |
147 | ANALOGS | 17 | 231 | 1799 |
148 | RATE | 40 | 230 | 1757 |
149 | LIGHT | 29 | 227 | 927 |
150 | CHANGE | 19 | 226 | 943 |
151 | CARBOXYHEMOGLOBIN | 11 | 225 | 443 |
152 | DIRECT | 15 | 220 | 1252 |
153 | CLINICAL | 22 | 219 | 800 |
154 | NORMAL | 32 | 215 | 1095 |
155 | PHOTODISSOCIATED | 10 | 212 | 374 |
156 | REDOX | 63 | 211 | 3329 |
157 | PATHWAYS | 13 | 210 | 3747 |
158 | NON | 33 | 208 | 1212 |
159 | OXY | 7 | 208 | 429 |
160 | QUATERNARY | 27 | 207 | 682 |
# | Word | Recs | TLCS | TGCS |
161 | COBALT | 32 | 205 | 1069 |
162 | NUCLEIC | 27 | 204 | 1694 |
163 | STRUCTURES | 37 | 203 | 2381 |
164 | OBSERVATION | 16 | 201 | 840 |
165 | REBINDING | 15 | 201 | 700 |
166 | THERMODYNAMICS | 18 | 201 | 1734 |
167 | REDUCTION | 42 | 200 | 1313 |
168 | SORET | 9 | 200 | 422 |
169 | IMPLICATIONS | 32 | 196 | 2774 |
170 | OXIDATION | 51 | 193 | 2119 |
171 | PHOSPHATE | 16 | 192 | 576 |
172 | HETEROGENEITY | 11 | 191 | 468 |
173 | ORIENTATION | 35 | 191 | 1256 |
174 | DERIVATIVES | 37 | 189 | 1040 |
175 | CONTROL | 19 | 188 | 1131 |
176 | TRANSITION | 58 | 185 | 2832 |
177 | COOLING | 8 | 183 | 469 |
178 | FETAL | 23 | 182 | 732 |
179 | PORPHYRINS | 37 | 182 | 1980 |
180 | COMPARISON | 29 | 181 | 1028 |
181 | APPROACHES | 8 | 180 | 512 |
182 | HYBRID | 21 | 179 | 489 |
183 | SYNTHETIC | 23 | 179 | 2002 |
184 | HORSE | 27 | 177 | 1984 |
185 | INTERACTION | 33 | 177 | 1589 |
186 | QUANTUM | 18 | 176 | 424 |
187 | DOUBLE | 20 | 175 | 749 |
188 | GLOBIN | 34 | 174 | 3344 |
189 | OXIDIZED | 25 | 174 | 1444 |
190 | ANTISICKLING | 27 | 173 | 540 |
# | Word | Recs | TLCS | TGCS |
191 | RELATIONSHIP | 14 | 173 | 473 |
192 | ASSOCIATION | 27 | 172 | 1636 |
193 | VOLUME | 27 | 171 | 2611 |
194 | ANOMALOUS | 3 | 170 | 284 |
195 | EXCITATION | 17 | 170 | 583 |
196 | ION | 27 | 170 | 1554 |
197 | DISSOCIATION | 17 | 169 | 468 |
198 | SUPERSATURATION | 3 | 169 | 198 |
199 | PARTICIPATION | 6 | 168 | 253 |
200 | REDUCED | 35 | 167 | 1265 |