We further developed a linear model using limma to correct the spot-specific dye bias [55].
We further developed optical imaging to temporally and spatially monitor the biodistribution of DTCSH.
We further developed allele-specific PCR primers to identify each of the seven QTLs.
After classes, we also had design-thinking workshops at Stanford's, where we further developed our concepts into working prototypes.
We further developed a cheap, fast, and simple method for fabricating micromolded structures using the crack patterns as templates.
We further developed relativistic time-centering methods for injection and we added methods to calculate higher order accurate position.
We further developed models to map flooded forest at a riparian site that experienced severe tree dieback.
We further developed a kinematic analysis approach to study dynamic root growth responses to auxin at high spatiotemporal resolution.
We further developed a new and effective preservation medium for cell sheets derived from the oral mucosal epithelium and their stem cells, as well as from human corneal tissue.
We further developed an assay to examine the phenotypic consequence of such diverse integration events and found that phage integration can cause changes in evolutionarily relevant traits such as bacterial motility and increases in antibiotic resistance.
We further developed a kinetic model with which we simulated the dynamic evolution of stress and composition in the thin-film cell.
