Skip to content

Instantly share code, notes, and snippets.

@allaway
Last active December 14, 2022 23:05
Show Gist options
  • Select an option

  • Save allaway/b7d851ce3440ad65cdd716ef454f940d to your computer and use it in GitHub Desktop.

Select an option

Save allaway/b7d851ce3440ad65cdd716ef454f940d to your computer and use it in GitHub Desktop.
Synodos NF2 kinome baseline data
library(synapser)
synLogin()
library(dplyr)
library(readr)
library(ggplot2)
#Looking at my old analysis scripts (bit messy...sorry), it looks like the baseline kinome data is in a different file, the experiment
#was probably done before any drug screening had taken place (hence the drug-pertubed kinome analysis was done seperately and later)
#There's also no syn6. My _guess_ is that this cell line was not tested at the time. Note that Syn1/Syn5 are the isogenic CRISPR pair,
#Syn6 is also known as Ben-Men-1 and is a well known NF2-/- cell line, but has no isogenic control in the Synodos data
#https://github.com/Sage-Bionetworks/Synodos_NF2/blob/master/kinomeAnalysis/kinomeTranscriptomeIntegration.R
kinome <- synGet('syn6182638')$path %>%
readr::read_tsv()
single_kinase_plot <- kinome %>%
filter(Gene == "YourKinaseHere",
cellLine == "Syn5",
referenceSample == "Syn1") %>% ##three replicates of each, but analysis was done pairwise to generate 9 different AXL ratios
ggplot2::ggplot(aes(x = Gene, y = ratio)) +
geom_boxplot() +
geom_point()
Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment