Custom Analysis part 2 - veeninglab/BactMAP GitHub Wiki
In the folder “Fig5D-H” you can find the analysis of a 2 minute interval
time-lapse movie. I used
SuperSegger
to
track the cells and get the cell outlines, while I used
iSBatch
`s
single-molecule biophysics imageJ
plugin
to track DnaX foci. To find more information on this dataset, check its documentation page.
To import the image stack DnaX-GFP.TIF
, use
extr_OriginalStack()
. Note that these files are all bigger than what we worked with before, this, for instance, is a
time-lapse of 115 images.
To make sure R has enough memory to handle bigger datasets, it is recommended to restart your R session before loading. Check the section on dealing with larger datasets for this and other tips on working with heavier data when using BactMAP.
image_custom <- extr_OriginalStack("Fig5D-H/DnaX-GFP.tif")
Use
extr_SuperSeggerCells()$mesh
to get the cell tracks and outlines.
extr_SuperSeggerCells()
takes the cell masks of each individual cell from thecellxxxx.mat
-files in thexy1//cell
folder, and the cell properties (length, width, etc) from the correspondingclist
. Note that below, I put “frames=1”. This is because this timelapse is taken on only one position, namely “xy1”. I set “timelapse=TRUE”.
cells_custom <- extr_SuperSeggerCells("Fig5D-H/supseg", frames=1, mag="100x_DVMolgen", startframe=1, timelapse=TRUE)$mesh
Check the content of the mesh file using summary(cells_custom)
and
View(cells_custom)
.
⬅️ Custom Analysis Part 1: Before Getting Started | Custom Analysis Part 3: Filtering the Data ➡️ |
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