Hello all!

I am analyzing adipocyte areas in human subcutaneous adipose tissue sections. I have scanned whole-slide images, which are in SVS file format. I am extracting portions of these images as TIF files and analyzing them in Fiji ImageJ. My question is: How can I measure all the extracted TIF files simultaneously in ImageJ? I have attempted to record my commands and import them for batch analysis, but I consistently seeing macro errors.

Thank you in advance!

Sreyasi