Viruses present an enormous diversity due to their high mutation rate, short replication time, and high number of replicates.
We proposed that if mtDNA deletion species have a replicative advantage over wild-type, based on a smaller size and faster replication time, larger mtDNA deletions would display the same replicative advantage over smaller mtDNA deletions.
overhead of secondary indices by treating them as data replicas during replication time.
These not only include iterative decomposition, pipelining, replication, time sharing, algebraic transforms, retiming, loop unfolding, and pipeline interleaving, but also bit-serial architectures, distributed arithmetic, and other not-so-common concepts.
The authors put forth the ribosome as an example of a natural molecular machine; because the ribosome suffers from neither problem, they must not be fundamental, saying: The authors also questioned Smalley's figures for the replication time of nanomachines.
In this work we aimed at quantifying effects that influence DNA replication time in budding yeast.
We have demonstrated a strong correlation between segment length and replication time.
We therefore normalized replication time with respect to S phase length.
It seems intuitive that the larger the segment of DNA is, the longer the replication time.
Here, we aimed at quantifying to which extent sequence properties contribute to the DNA replication time in budding yeast.
This means that, if the replication time is longer than average, the rate would be decelerated and vice versa.
