This includes 73 model refinement strategies as well as 30 identified medium-specific regulatory constraints.
First, we identify medium (PSLRair, PSLRwat for air and water, respectively) and substrate (PSLRsub) modes corresponding to the coupling of individual plasmon oscillations at medium- and substrate-related diffraction cut-off edges.
To maximize the likelihood of identifying medium penetrance genetic variants influencing T2D-risk, a total of 591 individuals of British ancestry, ascertained for early-adult onset (sample 1, n = 84), and/or family history of T2D (at least 1 sibling affected, sample 2, n = 507) were included (Table 1).
While the proposed sample size is small, the repeated measures design ensures our study is sufficiently powered to identify medium effects on our primary outcome variable, and provide preliminary assessment of the mechanisms of change.
We present a cost-effective method for identifying medium-sized deletions in genomic regions with low genomic coverage.
We provide an approach to accurately identify medium-sized deletions in large genomes with low sequence coverage.
This result suggests that an SR approach, in which split reads were used for identifying breakpoints of deletions, was effective for identifying medium-size deletions.
In this study, we showed that sequencing both ends of the restriction fragments generated by a medium-frequency enzyme can be an accurate method for identifying medium-sized deletions, even with sequence coverage as low as one-fold genome size.
In this study we identify medium-length ncRNAs (50-250 nt) from small RNA based sequencing data, characterize the RNase MRP of G. intestinalis, and clarify annotations of RNase P and MRP from both G. intestinalis and T. vaginalis.
In this specific case, the authors first screen carbon and nitrogen sources to identify key medium ingredients and then develop an experiment design approach to optimize chemical composition of the cultivation medium and temperature of incubation.
