Sentence examples for secondary sequences from inspiring English sources
The consensus macaque sequences were aligned and fixed divergent sites between macaque and humans were mapped onto secondary sequences.
The number of main and secondary sequences are the same as in the data set of [ 20].
OligoGenerator takes as input the number of target (main) sequences, the number of variations for each sequence (secondary sequences), and the length of each sequence.
That means, we divide TP to the number of all hits in all secondary sequences: In our example in Figure 3 the oligo 1 is hit twice, whereas the other hit sequences are hit only once each.
The results obtained by the students were that they established direct links between lattice walks and primary RNA sequences of YF and epilepsy and used lattice walks modeled by Riordan matrices to predict more stable RNA secondary sequences related to these two diseases.
One hundred eighteen unique sequences, encoding 124 proteins, were mapped to the B. cenocepacia genome (Additional file 2, Table S1); of these sequences, four were secondary sequences within an already identified gene, two were within a duplicated region on chromosome one, and one was a transposase gene with nine identical copies distributed throughout the genome.
Similar to PSS, secondary sequence is also positioned in the centre 62 REs nullifying the DC subcarrier.
In order to identify the primary and secondary sequencing of coupling elements, the Extension Analytic Hierarchy Process (EAHP) was adopted to analyze the contribution of each coupling element to the coupling functional system.
Thus, the influence weight factor of each coupling element can be determined, so as to provide a new approach for solving primary and secondary sequencing problem of coupling elements in a quantitative way, and facilitate the subsequent bionic coupling study.
Using separate motion control passes on the set, Knoll shot the lower of the upper torso and the secondary sequence with Krige's entire body.
The secondary sequence typing approach (gyrA/katG and pncA genes) revealed a CAS-lineage specific silent C->T mutation in codon 65 of the pncA gene.
