After developing and validating this method using TaPFT1, we applied it to the detection of homoeologue deletions of three additional target genes (TaNFXL1, TaCesA8 and TaPLDβ1) and successfully identified multiple deletions for each within the HII population (Table 2).
Our assay system confirmed this result, further validating this method.
After validating this approach, we further tested the performance of the method by enriching mcrA sequences from a complex methanogenic freshwater environment.
After validating the method, it is found that ROV has more instabilities in middle part of Persian Gulf and buoy (2) performs slightly better than buoy (1).
We validate this method by tracking the circulation and tissue distribution of MU-P loaded liposomes after intravenous administration.
We have validated this method only in semi-arid regions.
To validate this method, we apply it to the microarray data sets that measure gene expression changes in cell lines after transfection or inhibition of several specific miRNAs.
Second, we validated this method by a blind classification of modern mammalian teeth.
We therefore validated this method.
Further studies to validate this method further are planned.
