In 10% of samples, automated analysis identified a novel G873R substitution mutation in EGFR.
In total from all samples, proteomic analysis identified 59 dockerin- and 8 cohesin-module containing components, including 16 previously undetected cellulosomal subunits.
In these two samples, PRA analysis identified M. immunogenum type 2 (HaeIII—200, 70, 60, 55 bp and BstEII 320, 130 bp).
In Carver and White, a large-sample factor analysis identified a unidimensional BIS sensitivity measure and three BAS sensitivity subdimensions: BAS Drive, BAS Fun-seeking, and BAS Fun-seekingonsiveness.
In contrast to the clear influence resulting from year of sampling, differential expression analysis identified only two statistically significant sexually dimorphic differences in the RNA-Seq dataset and none in the microarray dataset.
In a sample analysis, we identified the two best and the two worst practices (Table 3).
Although there was a clearer difference between the aontrol and OA sample profiles, this unsupervised analysis identified no definitive disease duration-dependent difference in expression profiles of SF high-abundance proteins in OA patients.
Among down-regulated genes in the Coriell-18 sample set, Onto-Express analysis identified "immune response," "response to virus," and 'innate immune response" as highly statistically significant ontological categories (Additional file 6).
The DNA Detection Kit identified a pathogen in 11.3% (45/400) of the samples, and blood culture analysis identified a pathogen in 8.0% (32/400) of the samples.
Of the influenza-positive samples, RT-PCR/ESI-MS analysis identified 186 as influenza A virus and 67 as influenza B virus, in complete agreement with conventional typing methods.
