DRISEE bases its error estimates on variation from a consensus sequence in bins of artificially duplicated reads (ADRs).
RPB1, the largest subunit of RNA polymerase II, contains a highly modifiable C-terminal domain (CTD) that consists of variations of a consensus heptad repeat sequence (Y1S2P3T4S5P6S7).
Where there was disagreement, four researchers (ZA, AS, MS, MW) met to discuss the variation in results and reach a consensus decision, which in some cases required retesting.
In spite of many works on solar variations, there is not yet a consensus on the global experimental phenomenology.
Nuclei in STB exhibit a spectrum of morphologies and packing densities and, until recently, there seemed to be a consensus that this variation reflected a transition from an early undifferentiated CTB-like phenotype to a long pre-apoptotic and brief apoptotic phase.
It is of note, however, that the measurement of testosterone in the mouse is notoriously unreliable and large numbers of animals are often required to form a consensus on any variation from normal levels.
In these cases, no variant can be detected in one of the read types (i.e. the consensus sequence is non-ambiguous in one of the read types), but the opposing read type exhibits variation (ambiguous consensus) at a given position (e.g. T/T/W).
A consensus tree based on variation of core genes gives much better resolution than 16S and MLST; the pan-genome family tree is similar to the consensus tree, but with higher confidence.
In this study, values of the time and money needed to implement data standards were based on a consensus amongst researchers; nevertheless, variations could occur.
Because the nomenclatures of these variations require much more effort to reach a consensus.
