In comparison to these highly conserved orthologs which mediate the core cellular processes, we detect evidence of considerably less negative selection acting on orthologs associated with transmembrane receptors, apoptotic signals, guanyl-nucleotide exchange factors and GPCR activity.
During this process, we detected a small subset of sequences that are related to STEVOR proteins but do not have a high enough HMM score.
Fourth, during the re-annotation process we detected 142 situations in which a putative functional gene had been split in an ORF included in the primary annotation as a functional gene and a pseudogene detected in our FASTA and BLASTP searches.
For biological process ontology, we detected an enrichment of some categories in the training set (adj. p-value < 0.1) compared against the terms for the complete human genome dataset used in CART procedure.
Using our science-process skills test, we detected statistically significant increases in the use of quantitative terms in data analysis, understanding of controls, and designing an experiment appropriate to the goal of investigation.
However, using a science-process skills test, we detected a statistically significant increase in students' ability to propose an experiment that matches the goals of investigation, interpretation of controls, and quantitative analysis of data, but we did not see a similar increase in responses to questions assessing the skills of inference and evaluation.
Most importantly, at no point in the process did we detect any build-up of reactive diazo species.[ 12] It is important to ensure that the diazo species does not build-up if proceeding beyond small laboratory scale since these compounds can be highly energetic.
We detected process motility in 5 out of 11 dye-labeled NG2/EYFP cells (Fig 10A).
Although in the process we have detected what we suspect are alternative polyadenylation sites, focusing on them here would detract from the main findings of this work.
To ensure that the cultured cells were not contaminated with other cells throughout the process, we had detected SM α-actin, vimentin, SM-myosin, desmin and CD31 by immunohistochemical method as described in our previous study (Feng et al. 2012).
