library(knitr) ## use pngquant to reduce size of PNG images knit_hooks$set(pngquant = hook_pngquant) pngquant <- "--speed=1 --quality=0-25" # in case pngquant isn't available if (!nzchar(Sys.which("pngquant"))) pngquant <- NULL
options(width = 40)
## some frequently used HTML expressions Zc <- "<i>Z</i><sub>C</sub>" nH2O <- "<i>n</i>H<sub>2</sub>O" nO2 <- "<i>n</i>O<sub>2</sub>"
This vignette runs the code to make the plots from the following paper:
Dick JM. 2021. Water as a reactant in the differential expression of proteins in cancer. Computational & Systems Oncology 1(1): e1007. doi: 10.1002/cso2.1007
This vignette was compiled on r Sys.Date()
with JMDplots r packageDescription("JMDplots")$Version
and canprot r packageDescription("canprot")$Version
.
library(JMDplots)
The QEC basis species (glutamine, glutamic acid, cysteine, H~2~O, O~2~) are used for the analysis of stoichiometric hydration state (r nH2O
).
canH2O1()
r nH2O
and r Zc
for cell culture and cancer tissue (Figure 2)canH2O2()
r nH2O
-r Zc
plots for TCGA and HPA datasets (Figure 3)canH2O3()
canH2O4()
Mean differences are followed by log~10~ of p-value in parentheses. Mean differences are computed as (mean of median values for up-regulated proteins in each dataset) - (mean of median values for down-regulated proteins in each dataset). The rows labelled "up" and "down" refer to (mean of median values for [up- or down-]regulated proteins in secreted proteins in hypoxia) - (mean of median values for [up-or down-]regulated proteins in whole-cell extracts in hypoxia).
kable(canH2OT2(), align = "r")
kable(canH2OT1())
r nO2
-r Zc
and r nH2O
-r Zc
correlations using QEC basis species (Figure S1)canH2OS1()
r Zc
and r nH2O
(Figure S2)canH2OS2()
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