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At T ≈ 30°C, field-induced desorption of both a 12 mer as well as a 48 mer yielded a streptavidin-biotin disruption force of 75 fN.
An attempt was made to calculate the number of decoys for a 20 mer as well as for a 25 mer, to verify that the number fit these results.
Using the redox-active DNA conjugate (ferrocene-modified oligonucleotide 12 mer) as a probe, the novel electrochemical gene sensor, which is sensitive, convenient, and not relying on radio isotope, has been developed.
Our results identify Mer as a receptor uniquely capable of both tethering ACs to the macrophage surface and driving their subsequent internalization.
We first represent the k-mer as an integer (where each base corresponds to two bits).
To make the method computationally efficient, we treat each k-mer as an independent feature.
Treating each k-mer as an independent feature allows us to execute these steps fast and on the fly without storing the intermediate results.
Instead, Trinity built a K-mer dictionary from all clean reads based on frequency and considered each K-mer as an initial contig.
Representing each k-mer as an integer in, slice s consists of those k-mers whose remainder on division by S is s.
We used the median contig length (N50) generated for each k-mer as an indicator of the transcript contiguity of de novo assembly.
The best results (100% in 70 h) obtained in recycling mode with a rhodium complex as electrochemical mediator showed the potentiality of UF-MER as a process coupling a catalytic system and an electrochemical reaction.
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