| number | R Documentation | 
Given a time stack of images, number() performs a calculation of the number
for each pixel.
number(
  img,
  def,
  thresh = NULL,
  detrend = FALSE,
  quick = FALSE,
  filt = NULL,
  s = 1,
  offset = 0,
  readout_noise = 0,
  gamma = 1,
  parallel = FALSE
)
| img | A 4-dimensional array of images indexed by  | 
| def | A character. Which definition of number do you want to use,  | 
| thresh | The threshold or thresholding method (see
 | 
| detrend | Detrend your data with  | 
| quick | 
 | 
| filt | Do you want to smooth ( | 
| s | A positive number. The  | 
| offset,readout_noise | Microscope acquisition parameters. See reference Dalal et al. | 
| gamma | Factor for correction of number  | 
| 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  | 
A matrix, the number image.
Digman MA, Dalal R, Horwitz AF, Gratton E. Mapping the Number of Molecules and Brightness in the Laser Scanning Microscope. Biophysical Journal. 2008;94(6):2320-2332. \Sexpr[results=rd]{tools:::Rd_expr_doi("10.1529/biophysj.107.114645")}.
Dalal, RB, Digman, MA, Horwitz, AF, Vetri, V, Gratton, E (2008). Determination of particle number and brightness using a laser scanning confocal microscope operating in the analog mode. Microsc. Res. Tech., 71, 1:69-81. \Sexpr[results=rd]{tools:::Rd_expr_doi("10.1002/jemt.20526")}.
Hur K-H, Macdonald PJ, Berk S, Angert CI, Chen Y, Mueller JD (2014) Quantitative Measurement of Brightness from Living Cells in the Presence of Photodepletion. PLoS ONE 9(5): e97440. \Sexpr[results=rd]{tools:::Rd_expr_doi("10.1371/journal.pone.0097440")}.
img <- ijtiff::read_tif(system.file("extdata", "50.tif", package = "nandb"))
ijtiff::display(img[, , 1, 1])
num <- number(img, "N", thresh = "Huang")
num <- number(img, "n", thresh = "tri")
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