Exact(2)
Sequencing analysis revealed a somatic, non-synonymous mutation in NRAS (chr1 115,256,529 T > C, Q61R) at a comparable allele fraction (mean of 50%, range 40-73%) in all six tumor samples assessed, including 3 samplings from the original SBT and 3 from the first recurrence of LGSC (2 from rectosigmoid and 1 from the left pelvic sidewall).
This variation in drug concentrations did not correlate with changes in plasma raltegravir levels (Figure 2B), despite all 3 samplings being taken at a similar, relatively late time in the dosing interval (8.5 10 hours).
Similar(58)
There were 3 sampling time points, giving a total of 6 tanks per treatment.
However, the case study presented provides insight in the understanding of the general behavior of the 3 sampling design approaches.
†Indicates sampling during the dry season (June September); 2nd 4th samplings were conducted during a 2-year period.
From 1976 to 2010, 29 samplings were taken.
(3.6) We performed 100 samplings, each starting from different random initial points (i.e., (I := 100)) and averaged their results.
We performed 100 samplings, each starting from different random initial points given by MATLAB, and averaged their results.
MDA levels were significantly higher in Metis than in Pointe-au-Père for 7 samplings attesting a greater lipid peroxidation.
During the LK1, LK2 and LK3 samplings, δ34Szvs was not measured due to the low concentration of zero-valent sulfur (ZVS).
Data from 10 samplings were averaged for each heart.
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