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Ameet_Berkeley
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library(wholebrain) | |
#set folder path | |
folder<-'/Users/ameetrahane/Lab/Widlbrecht_Lab/brain-tissue-analysis/sectioned_test_1' | |
setwd(folder) | |
subfolders <- list.dirs(path = ".", full.names = TRUE, recursive = TRUE) | |
data <- data.frame() | |
#map to atlas coordinates | |
#set cutting thickness in millimeters | |
distance.between.sections <- 0.1 | |
#assign coordinates to image 2, 10, 20 and 40. | |
#Just check where they are and then assign them coordinate AP to bregma. | |
#In this case 3.1, 2.26, 1.22 and -0.87 | |
coords<-map.to.atlas(image.number = c(2, 10, 20, 40), | |
coordinate = c(3.10 2.26 1.22 -0.87), | |
sampling.period = distance.between.sections, | |
number.of.sections = length(subfolders) ) | |
for (i in seq_along(subfolders)[-1]) { | |
setwd(subfolders[i]) | |
gray.scalefolder <- create.output.directory('grayscale', '.') | |
setwd(gray.scalefolder) | |
images <- get.images('..') | |
for(j in seq_along(images)){ | |
#convert to gray scale | |
rgb2gray(images[j], invert = FALSE) | |
} | |
img<- stitch('.', order = "right.&.down", type = "row.by.row", tilesize = 2040, overlap = 0.1, show.image = FALSE) | |
myfilter <- list(alim = c(20, 300), | |
threshold.range = c(147, 256), | |
eccentricity = 1000, | |
Max = 255, | |
Min = 0, | |
brain.threshold = 10, | |
resize = 0.08, | |
blur = 5, | |
downsample = 1) | |
seg<-segment(img, filter = myfilter, numthresh = 16, display = FALSE) | |
regi <- registration(img, filter = myfilter, coordinate = coords[i], display = FALSE) | |
#dataset <- inspect.registration(regi, seg, forward.warps = TRUE) | |
dataset<-get.cell.ids(regi, seg, forward.warp = TRUE) #better for looping to results displayed | |
#save output for this section so you can go back and edit it. | |
save(file=paste0(tools::file_path_sans_ext(basename(img)), '.RData'), seg, regi, dataset) | |
#make web output | |
makewebmap(img, | |
seg$filter, | |
registration = regi, | |
dataset = dataset, | |
) | |
data <- rbind(data, dataset) | |
setwd("../..") | |
} | |
write.csv(data, file = 'test_all_data.csv') | |
data <- read.csv('first_nine_data.csv') | |
perspective<-structure(list(FOV = 30, ignoreExtent = FALSE, listeners = 1L, | |
mouseMode = structure(c("trackball", "zoom", "fov", "pull" | |
), .Names = c("left", "right", "middle", "wheel")), skipRedraw = FALSE, | |
userMatrix = structure(c(0.495914697647095, 0.285875976085663, | |
-0.819965422153473, 0, -0.106600426137447, -0.917073547840118, | |
-0.384204119443893, 0, -0.861803472042084, 0.277941107749939, | |
-0.424315959215164, 0, 0, 0, 0, 1), .Dim = c(4L, 4L)), scale = c(1, | |
1, 1), viewport = structure(c(0L, 0L, 1280L, 720L), .Names = c("x", | |
"y", "width", "height")), zoom = 1, windowRect = c(0L, 45L, | |
1280L, 765L), family = "sans", font = 1L, cex = 1, useFreeType = TRUE), .Names = c("FOV", | |
"ignoreExtent", "listeners", "mouseMode", "skipRedraw", "userMatrix", | |
"scale", "viewport", "zoom", "windowRect", "family", "font", | |
"cex", "useFreeType")) | |
glassbrain(data, cex=2, spheres = TRUE) | |
par3d(perspective) | |
glassbrain(data, cex=2, device = FALSE, spheres = TRUE, high.res = TRUE) | |
rgl.snapshot(filename ='3dbrain_image.png') |
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