The references were analyzed to clarify the distribution of highly-cited papers, authors and journals.
Therefore, smaller, more tractable datasets consisting of combinations of sympatric and sister species and allopatric references were analyzed independently as recommended by Pritchard & Wen [ 107].
The three groups (disomy 8, trisomy 8, and references) were analyzed in relation to the gene density on each BAC clone by ascertaining, using a custom-made script, the number of annotated RefSeq genes on each consecutive clone.
Liver protein extracts from three wild type and three Sec24a gt/gt mice and 293T cells expressing RFP-tagged SEC24A, SEC24C or SEC24D as references were analyzed with the indicated antibodies.
Each reference was analyzed aiming to identify all the mentioned concerns covered and solutions provided.
Ideally, the relationship between the fracture incidence rate and the change in reference was analyzed by regression analysis with an adjustment for age, the number of clinical risk factors, and the T-score.
Non-inferiority of each test product compared to the reference was analyzed as specified by EN 1500 rev:2009; that is, non-inferiority was concluded if all of the Tukey 95% CIs were contained in the interval (-∞, 0.6]. In all statistical tests of differences, a level of 5% (i.e., P ≤ 0.05) was used to determine statistical significance.
This alignment relative to the reference was analyzed using an iterative algorithm to simultaneously identify recombinant sequence and construct a phylogeny based only on vertically inherited point mutations in the "clonal frame" of the genome, as described previously (Croucher et al. 2011) (fig. 1).
Performance of the MPC controller to track a varying speed reference is analyzed in further details.
Four biological replicates for both phenanthrene treated and reference were analyzed by qPCR.
