Each plasma sample was analyzed with 2 technical (independent analysis of the same extract) replicas.
Although culture conditions, including medium composition, temperature, CO2%, and cell-cell interactions, are standardized and the cell micro-environment is expected to be the same across replicas, it is likely that marginal changes happen by chance.
All chunks are distributed into the nodes based on the following rules: any two of the three replicas should not be in the same node; each replica is randomly assigned to a rack.
Otherwise, the parameter p k of the replica o i has to be enriched, i.e. we need further data which is not in the replica o i to enrich the value of the QoS parameter p k. Hence, the content o i.v0 of the replica o i is required to be the same as the replica o j, i.e. o i.v0 = o j.v0.
Double transformants were patched on the same medium and replica plated on selective medium lacking histidine for auxotrophy analysis as described.
To assess the specificity of variant callers, we conducted independent sequencing experiments on the same sample (technical replica) from each of 16 normal tissue samples.
For the same federate, multiple replicas are developed in software diversity manner by employing different synchronization approaches.
In order to experience the same spectrum, I replicas of the interpolated signal are transmitted to ensure that the whole frequency range of the original signal is used.
We carried out a REMS simulation of the same system, using replicas at 273, 285, 299, and 313 K, simulated for 1,000 exchanges attempted every 1 ps with ts of 200 fs, corresponding to aggregate MD time of 1 ns, equal to that of simulations using canonical MD without REMS.
We used a genome-wide approach, evaluating the differences in methylation of the same CGIs between replicas of the same cell line.
