Nothing
suppressMessages(library(dplyr))
suppressMessages(library(ggplot2))
suppressMessages(library(OlinkAnalyze))
document_example <- function()
# https://github.com/Olink-Proteomics/OlinkRPackage
{
# visualize the NPX distribution per sample per panel, example for one panel
olink_dist_plot(npx_data1 %>% filter(Panel == 'Olink Cardiometabolic')) +
theme(axis.text.x = element_blank(),
axis.ticks.x = element_blank()) +
scale_fill_manual(values = c('turquoise3', 'red'))
olink_qc_plot(npx_data1 %>% filter(Panel == 'Olink Cardiometabolic')) +
scale_color_manual(values = c('turquoise3', 'red'))
# identify bridge samples
bridge_samples <- intersect(x = npx_data1$SampleID,
y = npx_data2$SampleID)
# bridge normalize
bridge_normalized_data <- olink_normalization(df1 = npx_data1,
df2 = npx_data2,
overlapping_samples_df1 = bridge_samples,
df1_project_nr = "20200001",
df2_project_nr = "20200002",
reference_project = "20200001")
# t-test npx_data1
ttest_results_NPX1 <- olink_ttest(df = npx_data1,
variable = "Treatment")
# select names of the top #10 most significant proteins
ttest_sign_NPX1 <- ttest_results_NPX1 %>%
head(n=10) %>%
pull(OlinkID)
# volcano plot with annotated top #10 most significant proteins
olink_volcano_plot(p.val_tbl = ttest_results_NPX1,
olinkid_list = ttest_sign_NPX1) +
scale_color_manual(values = c('turquoise3', 'red'))
}
# MGH data
# https://www.olink.com/application/mgh-covid-19-study/
HOME <- Sys.getenv("HOME")
dir <- file.path(HOME,"R","work","MGH","MGH_Olink_COVID_Apr_27_2021/")
NPX_data <- read_NPX(filename = file.path(dir,"MGH_COVID_OLINK_NPX.txt"))
# visualize the NPX distribution per sample per panel, example for one panel
olink_dist_plot(NPX_data %>% filter(Panel == 'Cardiometabolic')) +
theme(axis.text.x = element_blank(),
axis.ticks.x = element_blank()) +
scale_fill_manual(values = c('turquoise3', 'red'))
olink_qc_plot(NPX_data %>% filter(Panel == 'Cardiometabolic')) +
scale_color_manual(values = c('turquoise3', 'red'))
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