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Therefore, we can design an adaptive group commit mechanism, which takes into account the time of log persistence in each replica node.
In each replica, we selected five hundred random SNPs each explaining equal proportion of variance amounting to the total heritability minus 4%, and one random SNP explaining 4% of the phenotypic variance.
All the samples were assayed in triplicate, and in each replica, a minimum of three fields were counted and averaged.
Each time point consisted of two replicates with 10 zebrafish in each replica as well as the control group with comparable conditions.
Three independent RNAi gene-silencing assays were performed for each gene with two replicas each time (~30 mosquitoes in each replica).
Since we perform the clustering of CAGE data independently in each replica we need to integrate these results before being able to compare different biological samples.
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The version counter of every replica in a write quorum Q w is incremented so that the version counter of each replica in the quorum Q w shows the maximum value in the replica set O. Hence, the write quorum Q w includes at least one newest replica whose version counter is the maximum.
In the QB protocol, each replica has the version counter.
Availability is hard to achieve in the sense that each replica must have consistent data over a specified period.
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.
Each array was hybridized four times with four replicates per line, including two biological replications and two labeling replications in each biological replica.
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