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 1820, GCS 16259, CR 10393 Collection span: 1967 - 2011 | |
Word(i) List (944) Word count: 4054, All words count: 5949 |
# | Word | Recs | TLCS | TGCS |
---|---|---|---|---|
751 | MANGANESE | 1 | 0 | 2 |
752 | MANIPULATIONS | 1 | 0 | 2 |
753 | METALLOPROTEIN | 2 | 0 | 2 |
754 | MODULE | 1 | 0 | 2 |
755 | NARCOSIS | 1 | 0 | 2 |
756 | NUCLEAR | 2 | 0 | 2 |
757 | ORGANIC | 1 | 1 | 2 |
758 | PHOTO | 1 | 0 | 2 |
759 | POSSIBLE | 1 | 0 | 2 |
760 | PRECEDES | 1 | 0 | 2 |
761 | PROBING | 3 | 0 | 2 |
762 | RELEVANCE | 1 | 0 | 2 |
763 | REPLY | 1 | 0 | 2 |
764 | SHIFT | 2 | 0 | 2 |
765 | SOLUBILITY | 1 | 1 | 2 |
766 | SOLVENT | 1 | 0 | 2 |
767 | STUDIED | 2 | 0 | 2 |
768 | THEORIES | 1 | 0 | 2 |
769 | UPTAKE | 1 | 0 | 2 |
770 | VESICLES | 1 | 0 | 2 |
771 | ALGAL | 1 | 0 | 1 |
772 | BINDS | 2 | 0 | 1 |
773 | BIPHASIC | 1 | 0 | 1 |
774 | COMPLEXITY | 1 | 0 | 1 |
775 | DERIVATIVES | 1 | 0 | 1 |
776 | DESIGNS | 1 | 0 | 1 |
777 | DIMERS | 1 | 0 | 1 |
778 | ELECTROCHROMIC | 1 | 0 | 1 |
779 | EXCITON | 1 | 0 | 1 |
780 | GREEN | 1 | 0 | 1 |
# | Word | Recs | TLCS | TGCS |
781 | HELD | 1 | 0 | 1 |
782 | INEFFECTIVENESS | 1 | 0 | 1 |
783 | INTERIOR | 1 | 0 | 1 |
784 | MEETING | 1 | 0 | 1 |
785 | MOTIONS | 1 | 0 | 1 |
786 | MULTILAYERS | 2 | 0 | 1 |
787 | NOVEMBER | 1 | 0 | 1 |
788 | PARAMAGNETIC | 1 | 0 | 1 |
789 | PENETRATION | 1 | 0 | 1 |
790 | PRODUCTION | 1 | 0 | 1 |
791 | PROTEOLIPOSOMES | 3 | 0 | 1 |
792 | ROYAL | 1 | 0 | 1 |
793 | SOCIETY | 1 | 0 | 1 |
794 | SUBMICROMOLAR | 1 | 0 | 1 |
795 | VESICULAR | 1 | 0 | 1 |
796 | 4FE4S | 2 | 0 | 0 |
797 | ABSTRACTS | 1 | 0 | 0 |
798 | ADVANCES | 1 | 0 | 0 |
799 | AGENTS | 1 | 0 | 0 |
800 | ALFANO | 1 | 0 | 0 |
801 | ANGSTROM | 1 | 0 | 0 |
802 | ANISOTROPY | 1 | 0 | 0 |
803 | ARTIFICIAL | 3 | 0 | 0 |
804 | ASSESSMENT | 1 | 0 | 0 |
805 | B560 | 1 | 0 | 0 |
806 | B6F | 1 | 0 | 0 |
807 | BACKBONE | 1 | 0 | 0 |
808 | BACTERIUM | 1 | 0 | 0 |
809 | BARRIER | 1 | 0 | 0 |
810 | BASICITY | 1 | 0 | 0 |
# | Word | Recs | TLCS | TGCS |
811 | BCHL2 | 2 | 0 | 0 |
812 | BINARY | 1 | 0 | 0 |
813 | BRITTON | 1 | 0 | 0 |
814 | CALCULATED | 1 | 0 | 0 |
815 | CAPACITORS | 1 | 0 | 0 |
816 | CAPSULATAS | 1 | 0 | 0 |
817 | CAPTURE | 1 | 0 | 0 |
818 | CHANCE | 1 | 0 | 0 |
819 | CHARACTER | 1 | 0 | 0 |
820 | CHARACTERIZE | 1 | 0 | 0 |
821 | CHARGED | 1 | 0 | 0 |
822 | CHEMICAL | 1 | 0 | 0 |
823 | CHLOROPLAST | 1 | 0 | 0 |
824 | CHROMOPHORE | 1 | 0 | 0 |
825 | CIRCUIT | 1 | 0 | 0 |
826 | COHERENCE | 1 | 0 | 0 |
827 | COMPARISON | 1 | 0 | 0 |
828 | COMPARISONS | 1 | 0 | 0 |
829 | COMPLEXES | 4 | 0 | 0 |
830 | COMPUTER | 1 | 0 | 0 |
831 | CONDUCTIVITY | 1 | 0 | 0 |
832 | CONSTRUCTIONS | 1 | 0 | 0 |
833 | CONTRAST | 1 | 0 | 0 |
834 | COPOLYMERS | 1 | 0 | 0 |
835 | DEPLETED | 1 | 0 | 0 |
836 | DEPOSITION | 1 | 0 | 0 |
837 | DETERMINE | 1 | 0 | 0 |
838 | DEUTERATED | 1 | 0 | 0 |
839 | DEVELOPMENT | 1 | 0 | 0 |
840 | DIBLOCK | 1 | 0 | 0 |
# | Word | Recs | TLCS | TGCS |
841 | DISTRUBUTION | 1 | 0 | 0 |
842 | DYNAMIC | 2 | 0 | 0 |
843 | ELECTROSTATICALLY | 1 | 0 | 0 |
844 | ELEMENTARY | 1 | 0 | 0 |
845 | EMERGING | 1 | 0 | 0 |
846 | ENGINERIING | 1 | 0 | 0 |
847 | ENVIRONMENT | 1 | 0 | 0 |
848 | EXCITATION | 1 | 0 | 0 |
849 | FACTOR | 1 | 0 | 0 |
850 | FAST | 1 | 0 | 0 |
851 | FEATURES | 2 | 0 | 0 |
852 | FLAVO | 1 | 0 | 0 |
853 | FLOW | 2 | 0 | 0 |
854 | FORMED | 1 | 0 | 0 |
855 | GENERATED | 1 | 0 | 0 |
856 | GROUND | 1 | 0 | 0 |
857 | HEMEPROTEINS | 1 | 0 | 0 |
858 | HEMOPEPTIDES | 1 | 0 | 0 |
859 | HYDRATION | 2 | 0 | 0 |
860 | HYDROQUINONES | 1 | 0 | 0 |
861 | HYDROQUITIONE | 1 | 0 | 0 |
862 | IMAGE | 1 | 0 | 0 |
863 | IMPAIRED | 2 | 0 | 0 |
864 | INCORPORATED | 1 | 0 | 0 |
865 | INCORPORATING | 2 | 0 | 0 |
866 | INDIVIDUAL | 1 | 0 | 0 |
867 | INTERFACES | 3 | 0 | 0 |
868 | INTRA | 1 | 0 | 0 |
869 | INTRAPROTEIN | 1 | 0 | 0 |
870 | LABORATORY | 1 | 0 | 0 |
# | Word | Recs | TLCS | TGCS |
871 | LASER | 1 | 0 | 0 |
872 | LAURENS | 6 | 0 | 0 |
873 | LAYER | 1 | 0 | 0 |
874 | LECTURE | 1 | 0 | 0 |
875 | LIPOPEPTIDE | 1 | 0 | 0 |
876 | LIVED | 1 | 0 | 0 |
877 | LOCALIZATION | 1 | 0 | 0 |
878 | LONE | 1 | 0 | 0 |
879 | MAOUETTES | 1 | 0 | 0 |
880 | MATRIX | 1 | 0 | 0 |
881 | MEASURED | 1 | 0 | 0 |
882 | METALLOPORPHYRIN | 1 | 0 | 0 |
883 | METHOXY | 1 | 0 | 0 |
884 | METHYL | 1 | 0 | 0 |
885 | MIXED | 1 | 0 | 0 |
886 | MODELING | 1 | 0 | 0 |
887 | MODIFICATION | 1 | 0 | 0 |
888 | MODIFICATIONS | 1 | 0 | 0 |
889 | MOLECULES | 1 | 0 | 0 |
890 | MONO | 1 | 0 | 0 |
891 | MOTION | 1 | 0 | 0 |
892 | NAPHTHOQUINONE | 2 | 0 | 0 |
893 | NONNATIVE | 1 | 0 | 0 |
894 | OBITUARY | 6 | 0 | 0 |
895 | OPPORTUNITIES | 1 | 0 | 0 |
896 | OPTOELECTRICAL | 1 | 0 | 0 |
897 | OXIDO | 1 | 0 | 0 |
898 | P870 | 1 | 0 | 0 |
899 | PATHWAYS | 1 | 0 | 0 |
900 | PRESENCE | 1 | 0 | 0 |