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Flow cytometry data for "Regulation of macrophage polarization and plasticity by complex activation signals" (Smith, 2016).

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WendyLiuLab/BiactivationFlow

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To start working with a git checkout:

  1. Load the project in RStudio
  2. Run roxygen2 over the package by selecting Build -> Document
  3. Load the package with devtools::load_all()
  4. Run data-raw/preprocess.R
  5. Build -> Build and Reload

Summarized data files will be located in inst/extdata.

Column name Description
FSC.A Forward scatter AUC
FSC.H Forward scatter peak height
FSC.W Forward scatter peak width
SSC.* Side scatter; as above
CD86 Scale value for CD86 staining intensity
CD206 Scale value for CD206 staining intensity
Time Time to event from acquisition start (s)
Event.. Event serial number
Filename Filename of original FCS file
Experiment Replicate ID
antibody "exp" (CD206/CD86) or "iso" (isotype controls)
m1_concentration [LPS+IFN-γ] (ng/ml)
m2_concentration [IL-4+IL-13] (ng/ml)
timepoint (if applicable) Duration of incubation with cytokines (h)

See the vignettes for examples of normalizing data. Grouping on the antibody column is critical when plotting or summarizing data!

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Flow cytometry data for "Regulation of macrophage polarization and plasticity by complex activation signals" (Smith, 2016).

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