brightness_folder: Brightness calculations for every image in a folder.
In nandb: Number and Brightness Image Analysis

Description Usage Arguments See Also Examples

Perform brightness() calculations on all tif images in a folder and save the resulting brightness images to disk.

brightness_folder(
  folder_path = ".",
  def,
  thresh = NULL,
  detrend = FALSE,
  quick = FALSE,
  filt = NULL,
  s = 1,
  offset = 0,
  readout_noise = 0,
  parallel = FALSE
)

`folder_path`	The path (relative or absolute) to the folder you wish to process.
`def`	A character. Which definition of brightness do you want to use, `"B"` or `"epsilon"`?
`thresh`	The threshold or thresholding method (see `autothresholdr::mean_stack_thresh()`) to use on the image prior to detrending and brightness calculations.
`detrend`	Detrend your data with `detrendr::img_detrend_rh()`. This is the best known detrending method for brightness analysis. For more fine-grained control over your detrending, use the `detrendr` package. If there are many channels, this may be specified as a vector, one element for each channel.
`quick`	If `FALSE` (the default), the swap finding routine is run several times to get a consensus for the best parameter. If `TRUE`, the swap finding routine is run only once.
`filt`	Do you want to smooth (`filt = 'mean'`) or median (`filt = 'median'`) filter the number image using `smooth_filter()` or `median_filter()` respectively? If selected, these are invoked here with a filter radius of 1 (with corners included, so each median is the median of 9 elements) and with the option `na_count = TRUE`. If you want to smooth/median filter the number image in a different way, first calculate the numbers without filtering (`filt = NULL`) using this function and then perform your desired filtering routine on the result. If there are many channels, this may be specified as a vector, one element for each channel.
`s`	A positive number. The S-factor of microscope acquisition.
`offset`	Microscope acquisition parameters. See reference Dalal et al.
`readout_noise`	Microscope acquisition parameters. See reference Dalal et al.
`parallel`	Would you like to use multiple cores to speed up this function? If so, set the number of cores here, or to use all available cores, use `parallel = TRUE`.

number()

## Not run: 
setwd(tempdir())
img <- ijtiff::read_tif(system.file("extdata", "50.tif", package = "nandb"))
ijtiff::write_tif(img, "img1.tif")
ijtiff::write_tif(img, "img2.tif")
brightness_folder(def = "B", thresh = "Huang")

## End(Not run)