Title of dataset: Optical microscopy image data from Olympus BX51 for experimentA, Anon Lab Group Principal Investigator: Prof Anonymous, Research Institute, prof.anonymous@institute.edu Data Creator: John Smith, Research Institute, j.smith@institute.edu Project objectives: Investigate the effect of staining method on automatic cell identification in different regions of potato tubers --------------------------------------------DATA FILES------------------------------------------------- File naming convention: sizeSampleNum_zone_coreRegion_sectionNum_stain_imgNum.fileFormat Attributes: size = indicates potato tuber size according to mass (small, medium or large) SampleNum = a 2-digit number assigned to each tuber zone = one of three subregions of each tuber (bud, middle or stem) coreRegion = origin of the tissue core, either from the inner core (pith) or outer core (perimedullary) sectionNum = a 2-digit number assigned to sections from each core sample (between 01-05) stain = indicates one of four agents used for staining the tissue samples imgNum = a 2-digit number at the end of each image file fileFormat = 24-bit .tiff image files as generated by the microscope Acronyms and Codes: size = {small: "S", medium: "M", large: "L"} zone = {bud: "Z1", middle: "Z2", stem: "Z3"} coreRegion = {inner core: "IC", outer core: "OC"} stain = {None = blank, Safranin-O: "safo", Toluidine Blue-O: "tolu", Lugol's iodine: "lugol"} Examples: The first image of the 2nd thin section taken from the inner core of the bud zone of the 1st medium potato tuber, stained with safranin-O - M01_Z1_IC_02_safo_01.tiff ----------------- --------------------------DATA LOCATION----------------------------------------------- The raw image data is located in the following folder in the laboratory's central storage allocation: .../AnonLabGroup/ExperimentA/RawData/ Raw data folders are organised by strain then by treatment as shown below: RawData ├───Small ├ ├───Inner ├ └───Outer └───Medium ├───Inner └───Outer