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 404, GCS 46055, CR 26988, NA 5433 Collection span: 1991 - 2007 (17 years) | |
Title Word List (2075) Word count: 4279, All words count: 6226 |
# | Word | Recs | Percent | TLCS | TGCS |
---|---|---|---|---|---|
1401 | MONOMER | 1 | 0.2 | 0 | 71 |
1402 | MULTIELEMENT | 1 | 0.2 | 4 | 71 |
1403 | PEATS | 1 | 0.2 | 4 | 71 |
1404 | RELATIONS | 1 | 0.2 | 0 | 71 |
1405 | RETENTION | 1 | 0.2 | 0 | 71 |
1406 | SELECTIVITY | 1 | 0.2 | 0 | 71 |
1407 | TEMPLATE | 1 | 0.2 | 0 | 71 |
1408 | THEORIES | 1 | 0.2 | 0 | 71 |
1409 | TISSUES | 1 | 0.2 | 0 | 71 |
1410 | TRACE | 1 | 0.2 | 4 | 71 |
1411 | YOLK | 1 | 0.2 | 0 | 71 |
1412 | YTTRIA | 1 | 0.2 | 0 | 71 |
1413 | ZIRCONIA | 1 | 0.2 | 0 | 71 |
1414 | ALIPHATIC | 1 | 0.2 | 0 | 70 |
1415 | AMINES | 1 | 0.2 | 0 | 70 |
1416 | BUBBLE | 1 | 0.2 | 0 | 70 |
1417 | CLEAN | 1 | 0.2 | 0 | 70 |
1418 | CONDITION | 1 | 0.2 | 0 | 70 |
1419 | FLEXIBLE | 1 | 0.2 | 1 | 70 |
1420 | KAPPA | 1 | 0.2 | 0 | 70 |
1421 | OXIDIZED | 1 | 0.2 | 0 | 70 |
1422 | SHARPER | 1 | 0.2 | 0 | 70 |
1423 | SOLVABILITY | 1 | 0.2 | 0 | 70 |
1424 | STEADY | 1 | 0.2 | 0 | 70 |
1425 | VALUE | 1 | 0.2 | 0 | 70 |
1426 | VAPOROUS | 1 | 0.2 | 0 | 70 |
1427 | CURVES | 1 | 0.2 | 1 | 69 |
1428 | GROWTH | 1 | 0.2 | 1 | 69 |
1429 | REEXAMINING | 1 | 0.2 | 5 | 69 |
1430 | REFINED | 1 | 0.2 | 1 | 69 |
# | Word | Recs | Percent | TLCS | TGCS |
1431 | RNA | 1 | 0.2 | 1 | 69 |
1432 | SAGITTAE | 1 | 0.2 | 0 | 69 |
1433 | SERYL | 1 | 0.2 | 1 | 69 |
1434 | SUBGIANTS | 1 | 0.2 | 1 | 69 |
1435 | SUPEROUTBURST | 1 | 0.2 | 0 | 69 |
1436 | ANIONIC | 1 | 0.2 | 0 | 68 |
1437 | BI2SR2CACU2O8 | 1 | 0.2 | 0 | 68 |
1438 | BILAYERS | 1 | 0.2 | 4 | 68 |
1439 | CENTAURUS | 1 | 0.2 | 3 | 68 |
1440 | COLLISION | 1 | 0.2 | 0 | 68 |
1441 | CONDUCTOMETRIC | 1 | 0.2 | 0 | 68 |
1442 | DETERGENT | 1 | 0.2 | 0 | 68 |
1443 | DIP | 1 | 0.2 | 0 | 68 |
1444 | EXCLUDED | 1 | 0.2 | 3 | 68 |
1445 | HERBICIDES | 1 | 0.2 | 0 | 68 |
1446 | HUMP | 1 | 0.2 | 0 | 68 |
1447 | INTERDIGITATION | 1 | 0.2 | 4 | 68 |
1448 | K13 | 1 | 0.2 | 1 | 68 |
1449 | KILOMETER | 1 | 0.2 | 1 | 68 |
1450 | MOLA | 1 | 0.2 | 1 | 68 |
1451 | NUMBER | 1 | 0.2 | 3 | 68 |
1452 | PERMEABILIZATION | 1 | 0.2 | 0 | 68 |
1453 | PHENOMENOLOGICAL | 1 | 0.2 | 1 | 68 |
1454 | PHOTOEMISSION | 1 | 0.2 | 0 | 68 |
1455 | ROUGHNESS | 1 | 0.2 | 1 | 68 |
1456 | SCALE | 1 | 0.2 | 1 | 68 |
1457 | STUDYING | 1 | 0.2 | 4 | 68 |
1458 | VESICLES | 1 | 0.2 | 0 | 68 |
1459 | 2.1 | 1 | 0.2 | 1 | 67 |
1460 | ABSOLUTE | 1 | 0.2 | 0 | 67 |
# | Word | Recs | Percent | TLCS | TGCS |
1461 | ALOGPS | 1 | 0.2 | 1 | 67 |
1462 | ARBITRARY | 1 | 0.2 | 2 | 67 |
1463 | ARCHITECTURES | 1 | 0.2 | 0 | 67 |
1464 | AROMATIC | 1 | 0.2 | 0 | 67 |
1465 | ASSOCIATIVE | 1 | 0.2 | 1 | 67 |
1466 | BERGMANN | 1 | 0.2 | 0 | 67 |
1467 | BIGINELLI | 1 | 0.2 | 0 | 67 |
1468 | CEPHEIDS | 1 | 0.2 | 0 | 67 |
1469 | CHARM | 1 | 0.2 | 0 | 67 |
1470 | CLUSTER | 1 | 0.2 | 1 | 67 |
1471 | COALESCENCE | 1 | 0.2 | 0 | 67 |
1472 | CONSERVATION | 1 | 0.2 | 0 | 67 |
1473 | CRYOSURGERY | 1 | 0.2 | 0 | 67 |
1474 | CYTOPLASMIC | 1 | 0.2 | 0 | 67 |
1475 | EG5 | 1 | 0.2 | 0 | 67 |
1476 | EJECT | 1 | 0.2 | 0 | 67 |
1477 | ELECTROCHROMIC | 1 | 0.2 | 2 | 67 |
1478 | ENANTIOSEPARATION | 1 | 0.2 | 0 | 67 |
1479 | EXPANSIONS | 1 | 0.2 | 1 | 67 |
1480 | FOLLOW | 1 | 0.2 | 0 | 67 |
1481 | FUNCTIONALIZED | 1 | 0.2 | 0 | 67 |
1482 | GLIAL | 1 | 0.2 | 0 | 67 |
1483 | GRADIENT | 1 | 0.2 | 0 | 67 |
1484 | HEPATIC | 1 | 0.2 | 0 | 67 |
1485 | INHIBITOR | 1 | 0.2 | 0 | 67 |
1486 | INVESTIGATION | 1 | 0.2 | 0 | 67 |
1487 | KINESIN | 1 | 0.2 | 0 | 67 |
1488 | LIPOPHILICITY | 1 | 0.2 | 1 | 67 |
1489 | METASTASES | 1 | 0.2 | 0 | 67 |
1490 | MITOTIC | 1 | 0.2 | 0 | 67 |
# | Word | Recs | Percent | TLCS | TGCS |
1491 | MOBILIZATION | 1 | 0.2 | 0 | 67 |
1492 | MONASTROL | 1 | 0.2 | 0 | 67 |
1493 | MONODISPERSE | 1 | 0.2 | 0 | 67 |
1494 | NEIGHBOURHOOD | 1 | 0.2 | 0 | 67 |
1495 | OLIGOFLUORENE | 1 | 0.2 | 0 | 67 |
1496 | PART | 1 | 0.2 | 0 | 67 |
1497 | PATTERN | 1 | 0.2 | 1 | 67 |
1498 | RAS | 1 | 0.2 | 1 | 67 |
1499 | REACTIONS | 1 | 0.2 | 0 | 67 |
1500 | RISM | 1 | 0.2 | 2 | 67 |
1501 | SHAPED | 1 | 0.2 | 0 | 67 |
1502 | SOLUTE | 1 | 0.2 | 2 | 67 |
1503 | SPHERICALLY | 1 | 0.2 | 1 | 67 |
1504 | THERMODYNAMICAL | 1 | 0.2 | 0 | 67 |
1505 | TRUXENES | 1 | 0.2 | 0 | 67 |
1506 | TUMORS | 1 | 0.2 | 1 | 67 |
1507 | BA2 | 1 | 0.2 | 4 | 66 |
1508 | CHELATORS | 1 | 0.2 | 4 | 66 |
1509 | CLASSIFICATION | 1 | 0.2 | 0 | 66 |
1510 | CLONING | 1 | 0.2 | 0 | 66 |
1511 | CROWN | 1 | 0.2 | 4 | 66 |
1512 | DIGENEA | 1 | 0.2 | 0 | 66 |
1513 | FABRICATED | 1 | 0.2 | 0 | 66 |
1514 | FERROMAGNET | 1 | 0.2 | 0 | 66 |
1515 | FLUCTUATIONS | 1 | 0.2 | 0 | 66 |
1516 | FUMED | 1 | 0.2 | 0 | 66 |
1517 | INERT | 1 | 0.2 | 3 | 66 |
1518 | LINEAR | 1 | 0.2 | 0 | 66 |
1519 | MATRICES | 1 | 0.2 | 3 | 66 |
1520 | MG2 | 1 | 0.2 | 4 | 66 |
# | Word | Recs | Percent | TLCS | TGCS |
1521 | NEOPLASMS | 1 | 0.2 | 2 | 66 |
1522 | OXIDES | 1 | 0.2 | 0 | 66 |
1523 | P70 | 1 | 0.2 | 0 | 66 |
1524 | PHYLOGENY | 1 | 0.2 | 0 | 66 |
1525 | PLATYHELMINTHES | 1 | 0.2 | 0 | 66 |
1526 | PROXIMITY | 1 | 0.2 | 0 | 66 |
1527 | ROTAMERIZATION | 1 | 0.2 | 3 | 66 |
1528 | SUSPENSION | 1 | 0.2 | 0 | 66 |
1529 | T1796A | 1 | 0.2 | 2 | 66 |
1530 | TRANSVERSION | 1 | 0.2 | 2 | 66 |
1531 | TREMATODA | 1 | 0.2 | 0 | 66 |
1532 | ZETA | 1 | 0.2 | 0 | 66 |
1533 | AEROSOL | 1 | 0.2 | 0 | 65 |
1534 | ARRAY | 1 | 0.2 | 0 | 65 |
1535 | ASSOCIATES | 1 | 0.2 | 2 | 65 |
1536 | ATLANTIC | 1 | 0.2 | 0 | 65 |
1537 | BINARY | 1 | 0.2 | 0 | 65 |
1538 | BIOSENSING | 1 | 0.2 | 0 | 65 |
1539 | CD95 | 1 | 0.2 | 2 | 65 |
1540 | CDW150 | 1 | 0.2 | 2 | 65 |
1541 | CODING | 1 | 0.2 | 1 | 65 |
1542 | CYGNI | 1 | 0.2 | 0 | 65 |
1543 | DILATON | 1 | 0.2 | 0 | 65 |
1544 | DISCOVERY | 1 | 0.2 | 0 | 65 |
1545 | DNA | 1 | 0.2 | 1 | 65 |
1546 | ECLIPSE | 1 | 0.2 | 0 | 65 |
1547 | ESTIMATE | 1 | 0.2 | 0 | 65 |
1548 | FTIR | 1 | 0.2 | 0 | 65 |
1549 | GRS | 1 | 0.2 | 0 | 65 |
1550 | HELP | 1 | 0.2 | 0 | 65 |
# | Word | Recs | Percent | TLCS | TGCS |
1551 | HOMOLOGY | 1 | 0.2 | 2 | 65 |
1552 | INTERFEROMETRY | 1 | 0.2 | 0 | 65 |
1553 | LOSS | 1 | 0.2 | 0 | 65 |
1554 | MICRO | 1 | 0.2 | 0 | 65 |
1555 | MODULATES | 1 | 0.2 | 2 | 65 |
1556 | NESDIS | 1 | 0.2 | 0 | 65 |
1557 | NOAA | 1 | 0.2 | 0 | 65 |
1558 | NONCODING | 1 | 0.2 | 1 | 65 |
1559 | NORTH | 1 | 0.2 | 0 | 65 |
1560 | PHOTOLUMINESCENCE | 1 | 0.2 | 1 | 65 |
1561 | PLASMON | 1 | 0.2 | 0 | 65 |
1562 | RADII | 1 | 0.2 | 0 | 65 |
1563 | RATE | 1 | 0.2 | 0 | 65 |
1564 | RNADS | 1 | 0.2 | 0 | 65 |
1565 | SATELLITE | 1 | 0.2 | 0 | 65 |
1566 | SCALAR | 1 | 0.2 | 0 | 65 |
1567 | SLIDING | 1 | 0.2 | 0 | 65 |
1568 | SRC | 1 | 0.2 | 2 | 65 |
1569 | STELLAR | 1 | 0.2 | 0 | 65 |
1570 | V444 | 1 | 0.2 | 0 | 65 |
1571 | VALIDATION | 1 | 0.2 | 0 | 65 |
1572 | VIS | 1 | 0.2 | 0 | 65 |
1573 | WATCH | 1 | 0.2 | 0 | 65 |
1574 | ALIGNMENT | 1 | 0.2 | 1 | 64 |
1575 | ANISOTROPIC | 1 | 0.2 | 1 | 64 |
1576 | BARIUM | 1 | 0.2 | 0 | 64 |
1577 | BOUNCING | 1 | 0.2 | 0 | 64 |
1578 | BRANEWORLDS | 1 | 0.2 | 0 | 64 |
1579 | BROWN | 1 | 0.2 | 0 | 64 |
1580 | COGNATE | 1 | 0.2 | 1 | 64 |
# | Word | Recs | Percent | TLCS | TGCS |
1581 | FE3O4 | 1 | 0.2 | 0 | 64 |
1582 | HEAT | 1 | 0.2 | 0 | 64 |
1583 | INACTIVATION | 1 | 0.2 | 0 | 64 |
1584 | LIQUIDS | 1 | 0.2 | 0 | 64 |
1585 | POLAR | 1 | 0.2 | 0 | 64 |
1586 | REACTANT | 1 | 0.2 | 0 | 64 |
1587 | REORGANIZATION | 1 | 0.2 | 0 | 64 |
1588 | SIGMA | 1 | 0.2 | 0 | 64 |
1589 | TEXTURE | 1 | 0.2 | 1 | 64 |
1590 | ACIDIC | 1 | 0.2 | 0 | 63 |
1591 | ANALOG | 1 | 0.2 | 0 | 63 |
1592 | CATARACTS | 1 | 0.2 | 0 | 63 |
1593 | COPIA | 1 | 0.2 | 0 | 63 |
1594 | ELECTRICALLY | 1 | 0.2 | 0 | 63 |
1595 | EXCITATION | 1 | 0.2 | 0 | 63 |
1596 | FROG | 1 | 0.2 | 1 | 63 |
1597 | GRATINGS | 1 | 0.2 | 0 | 63 |
1598 | HYPERICIN | 1 | 0.2 | 0 | 63 |
1599 | MAGNETOSTRAIN | 1 | 0.2 | 1 | 63 |
1600 | OCTAHYDROXY | 1 | 0.2 | 0 | 63 |