Sentence examples for maps we find from inspiring English sources

Using Schnabel's data to evaluate the corresponding wavelengths in real maps, we find that the quotient between (varLambda _{mathrm{sq}}) and (varLambda_{mathrm{mean}}) is about 1.1, and they are within 15%% of each other.

Strikingly, despite the low resolution of our maps, we find that the αβ-tubulin dimer adopts a unique conformation in the ternary complex.

From the predicted raIS maps, we find that the numbers of raIS elements in different cyanobacteria and archaea vary significantly, and many organisms don't harbor any raIS elements, as shown in the two phylogenetic trees for the 19 cyanobacteria and 31 archaea, respectively.

When comparing the genetic maps, we found that NIS1 could be allelic to the QTL 1.2 found by Talukder et al. (2005).

Simultaneously, inspecting the TEC maps, we found evidence for a turbulence in TEC propagating southward probably caused by large scale travelling ionospheric disturbances (LSTIDs) linked to auroral electrojet intensification.

Across both maps, we found 13 QTL for flowering time.

Reflecting on the experience of constructing the maps we found that the two diagrams each had advantages and disadvantages.

Using these maps, we found an overlap of 16.5 % between the inferior frontal cluster of GMV increase and one posterior inferior functional subunit associated with action imitation.

When we searched for the position of these nine markers in published maps, we found that seven out of nine markers were located on LG 7 in the published maps [ 18, 19].

To determine the position of eam5 on genetic and physical maps, we found closest flanking RFLP markers with known nucleotide sequences using the GrainGenes CMap browser (BinMap 2005; http://wheat.pw.usda.gov/cgi-bin/cmap).

In addition, with the MT maps we found that higher component scores related to facial identity were associated with increased grey matter volume in the right middle fusiform gyrus/ITG.