Un-induced GT efficiencies increase exponentially with template length (64), probably because the chance that a random chromosome DSB occurs within the homology region increases with template length.
Unexpectedly, with our templates increasing acceptor concentration increased the transfer efficiency but had no effect on the rate of transfer.
The Tg of AAO template-supported PMMA nanotubes increases with decreasing ttube, with Tg,tube − Tg,bulk = 12 K in 18-nm-thick nanotubes; we attribute the Tg increase to hydrogen bonds between PMMA ester side groups and hydroxyl groups on the surface of the γ-Al2O3 templates.
Moreover, we found that amplification failure of long alleles increased more than linearly with sample age, which is in accordance with DNA degradation and fragmentation being random processes, leading to an exponential decline in DNA template with increasing amplicon target size [ 14, 32].
The demand for the identification of user-defined templates of gene expression profiles increases with the availability of large-scale gene expression data when microarray or proteomic experiments cover whole cell cycles or other time evolving processes.
Microfocus XRD experiments show that the crystallite sizes increase with increased template hole size.
Here we use the same template approach to understand whether pore roughness increases with the increase of the etching time.
The fold of amplification increases with smaller quantities of template RNA, but the absolute yield of aRNA decreases.
In general, the average homology model accuracy is a function of the template-target sequence similarity: The dispersion of the model-target structural overlap increases with the decrease in sequence identity between template and target.
The proportion of failed reads due to process-related problems are more abundant in traces with lower average read lengths while the opposite trend showing template-related failures increasing with increased average read length is true.
