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Image SXM Changelog

What's new in Image SXM 205-3

Dec 7, 2022
  • Changes to macros:
  • Selecting a slice of a stack using 'SelectSlice' now updates the window title if each image in the stack has a different title.

New in Image SXM 205-2 (Dec 7, 2022)

  • Other changes:
  • Rotate raw SNOM images 90° clockwise to agree with image orientation from optical microscope, rather than image orientation displayed when images are opened in MATLAB.
  • Minor changes to astrophotography image processing routines.
  • VVG Stain Analysis algorithm for elastin and collagen modified for smaller images.

New in Image SXM 205-1 (Dec 7, 2022)

  • Added features:
  • A new 'VVG Stain Analysis' item has been added to the MIASMA menu.
  • Other changes:
  • Minor changes to routines for opening and processing SNOM images.

New in Image SXM 204-1 (Dec 7, 2022)

  • Other changes:
  • Minor changes to astrophotography image processing routines.

New in Image SXM 203-1 (Dec 7, 2022)

  • Added features:
  • Support has been added for Agilent PicoView SPM images.
  • Bug fixes:
  • Updated support for Nanoscope v9.2.
  • Bug fix in PrinCIPia routines for processing prestack.

New in Image SXM 202-1 (Apr 23, 2018)

  • Added features:
  • Added 'Random Grayscale' checkbox to 'LUT Options' dialog box.
  • Bug fixes:
  • When using the 'UpdateLUT' macro command the option key prevents LUT entry 0 being reset to white and LUT entry 255 being reset to black.
  • Changes to macros:
  • Added 'ApplyRandomLUT' macro command to apply random greyscale values to all 0-255 LUT entries. If its argument N is non-zero then this value will be used to determine the random numbers used in the LUT. If N = 0 then Image SXM will continue generating its own random seeds.

New in Image SXM 201-1 (Sep 13, 2017)

  • Added features:
  • Added routines to process stellar spectra produced by the Star Analyser 100 diffraction grating.
  • Other changes:
  • When browsing images the maximum image size has been increased from 256 to 512 pixels.
  • Minor changes to the 'Fibre Texture Analysis' routines.

New in Image SXM 200-2 (Jul 15, 2017)

  • Added features:
  • Support has been added for Hysitron TriboScan images.
  • Bug fixes:
  • The display of the prompting message in the 'GetString' macro function was inadvertently disabled.

New in Image SXM 200-1 (Apr 28, 2017)

  • Added features:
  • A new 'Fibre Texture Analysis' item has been added to the MIASMA menu.
  • Bug fixes:
  • In the Intel (X) version when loading Omicron SCALA STS data only some of the data was byte-swapped and so the STS did not display correctly.
  • When opening an RGB image creating an 8-bit indexed image would leave the RGB image stack displaying the wrong slice.
  • Other changes:
  • In NanoScope v9 SPM image file headers the image data is declared as 16-bit even though it is actually 32-bit. Image SXM now loads all NanoScope images pre-v9 as 16-bit and post-v9 as 32-bit.
  • As some 8-bit bitmaps are saved by third-party applications as 24-bit bitmaps, Image SXM checks for this when opening bitmaps and generates a warning dialog accordingly.
  • Modified the 'Image Correlation' routine with the addition of pixel correlation maps.

New in Image SXM 199-2 (Dec 10, 2016)

  • Added features:
  • Typing or clicking in a text window now shows the line and column position of the cursor in the Info window.
  • Bug fixes:
  • In the Intel version 'Update Stack Slice Titles' would result in opening stacks with undefined XY scales.
  • Changes to macros:
  • Added 'arctan2' macro command. It has two parameters (x, y) to provide the arctan of y/x with the angle in the appropriate quadrant.

New in Image SXM 199-1 (Aug 26, 2016)

  • Added features:
  • A new edge-preserving smooth (Epsilon) algorithm has been added, but is not yet a menu item. See also 'Changes to macros'.
  • Added support for JEOL JSM 7001F SEM images. On loading the XY scale is calibrated using the scale bar imprinted in the bottom right of the image.
  • A new 'Bacterial Membrane Analysis' item has been added to the MIASMA menu.
  • Bug fixes:
  • Bug fix and tidy up to LEED I-V routines when manually extracting spot intensities.
  • Changes to macros:
  • Added 'Epsilon' macro command (see above). Its argument N sets the size of the NxN ROI where 3

New in Image SXM 198-1 (Jul 30, 2015)

  • Added features:
  • A new 'Skeleton To ROI' item has been added to the Process/Binary submenu. This creates a free line ROI from the pixels in a skeletonised image. The skeleton should not have forks, junctions or loops. If the skeleton comprises separate objects then the command can be applied sequentially to each object. Each ROI is saved and can be restored using Options/Restore ROI. See also 'Changes to macros'.
  • Bug fixes:
  • In 'Bacterial MicroCompartments' analysis folder and file names are now truncated to avoid output filenames longer than 30 characters.
  • Other changes:
  • 'Prune Skeleton' is now a separate menu item in the Process/Binary submenu. The macro command is unchanged.
  • JPK images with 32-bit data values are now supported.
  • 'Windows to Stack' and 'Stack to Windows' for up to 1000 images is now more memory efficient.
  • Modified 'Microneedle Analysis' to handle breached epidermal layers.
  • Changes to macros:
  • The macro command 'SkeletonToROI' has been added (see above).
  • Added 'RotatingMask' macro command. Its argument N sets the size of the NxN mask where 3

New in Image SXM 197-2 (Jan 29, 2015)

  • Added features:
  • A new 'Microneedle Analysis' item has been added to the MIASMA menu.
  • Bug fixes
  • Fixed a bug to ensure that values calculated for a rectangular ROI agree with values for a whole image of the same region.
  • Fixed a bug affecting density slicing in magnified histogram windows when the image had an inverted z calibration.
  • Other changes:
  • Increased 'Image Correlation' plot size to 512x512.
  • Microcirculation Analysis now works with QuickTime movies rather than AVI files.

New in Image SXM 197-1 (Aug 26, 2014)

  • Constraining rectangles and lines to power-of-2 sizes to allow FFT operations now works by pressing the tab key (no shift key required) when the selection is being created or resized. Pressing tab before a mouse click suppresses the creation of a new selection.
  • Changes to 'Bacterial MicroCompartments' analysis:
  • Miscalculating bacteria lengths has been reduced.
  • Output of invalid values has been suppressed.
  • Added output of mean bacteria lengths and widths for all images in folder.
  • Added image map of compartment density.
  • Added overlay map of compartment locations.

New in Image SXM 196-3 (Mar 25, 2014)

  • Bug fixes:
  • Fixed a bug in the calculation of bounding boxes.
  • Other changes:
  • Suppressed the loading of hyperspectral data when browsing FTIR images.
  • The smallest image that can be opened is now 8 x 8 pixels.
  • Reduced the values of some global constants to reduce the size of static arrays.
  • Cancelling a dialog to save an image on quitting Image SXM cancels the Quit, not just the Save.
  • Changes to macros:
  • Added access to the array of modal density values (rMode) calculated using 'Measure' or 'Analyze Particles'.

New in Image SXM 196-2 (Feb 15, 2014)

  • Added features:
  • A new 'Merge RGB Stacks' item has been added to the Stacks menu. From separate stacks of red and green (or red, green and blue) images it creates a colour stack with the System LUT.
  • Support has been added for Varian hyperspectral FTIR images.
  • Bug fixes:
  • Fixed a bug affecting selection and dragging of COI windows in PrinCIPia.
  • Fixed a bug that caused the 'Preferences' menu item to appear twice in the 'Image SXM' menu.

New in Image SXM 196-1 (Jan 30, 2014)

  • ADDED FEATURES:
  • Unchecking 'Update Stack Slice Titles' from the Options > Preferences dialog box now suppresses slice title updates in stacks created from windows (as well as stacks loaded from files, as before).
  • BUG FIXES:
  • Applying '3-Point Compensation' to a 32-bit or 64-bit image now works correctly.
  • Fixed a bug affecting window updates after a copy-paste-close operation.
  • Fixed an incompatibility between the GNU Pascal compiler and CodeWarrior that resulted in some TIFF tags not being read correctly by other applications.
  • Fixed a bug affecting saved 24-bit colour images. The bug did not affect 24-bit RGB image stacks.
  • Bugs fixed in PrinCIPia routines:
  • Working on a CIPstack load from an earlier session could give inconsistent results.
  • 'Flatten Grain Map' gave incorrect colours if the window size was scaled below 100%.
  • OTHER CHANGES:
  • Changes to PrinCIPia routines:
  • The standard CLUT has been rotated so that North = green/yellow, East = red, South = blue/magenta, West = cyan.
  • Moving a COI window moves its associated Pole Figure and CLUT windows such that they stay to the right of their parent COI.
  • Closing a COI window closes its associated Pole Figure and CLUT windows.
  • CHANGES TO MACROS:
  • Macro command 'UpdatesOff' now has a more global effect on all screen updates, not just those involving ROIs.

New in Image SXM 195-2 (Sep 5, 2013)

  • Added features:
  • When stacks are loaded and the slices have individual names, then either (i) these names can be used to update the stack window title when the slices are selected, or (ii) the stack can retain its fixed title when the slices are selected. This option has a checkbox in the Options > Preferences dialog box.
  • The Histogram window can now be optionally displayed at a magnification factor of x2. This option has a checkbox in the Options > Preferences dialog box.
  • Bug fixes:
  • Fixed a bug that could affect switching between windows, leaving the current (active) window undefined.
  • Resolved an ambiguity between different types of AFM images having a common '.afm' file suffix.
  • Fixed a bug that prevented a Zoom window (created with z-click or shift-Z-click) from updating correctly. The Zoom window is a small window showing a magnified view of the region of the image around the cursor (default 2x magnification, 4x if the shift key is also pressed).
  • Other changes:
  • Changes to LEED I-V routines: (i) minor changes to tracking algorithm; (ii) fixed bug affecting small values of allowed tracking error; (iii) sorted LEED spot output into order of distance from centre of LEED pattern; (iv) minor changes to format of output files.
  • Constraining ROIs to be a power-of-2 sized square now uses the shift and tab keys.
  • When clicking in a stack window, cmd-space (magnifier tool) takes priority over cmd (scroll through stack).
  • 'Size Distribution' now works for radii up to 1000.
  • When doing a Rodbard fit to density calibration data, if negative fit parameters are produced that result in an invalid fit then those parameters are reset to zero. This was unnecessary with versions of Image SXM written in Motorola code, but can cause problems with Intel versions. If you use Rodbard fits to calibration data then I suggest you check the results and email me if you see any inconsistencies between different versions of Image SXM.
  • Added support for raw NEF images from Nikon D7100 DSLR cameras.
  • Changes to macros:
  • Macro command 'UpdatesOff' now has a more global effect on all screen updates, not just those involving ROIs.

New in Image SXM 195-1 (May 7, 2013)

  • Added features:
  • A new 'Pincushion/Barrel Distortion' item has been added to the Process menu. Click on the 4 vertices of a pincushion or barrel shape that, after correction, will appear square. Then click on the 4 mid-points of the sides of the shape. If the image is a slice in a stack, then all the slices of the stack will be corrected. Press the option key and select 'Set Pin/Barrel Options' to change the number of vertices and sides from 4 to 3 (ie, squares to triangles).
  • A new 'Distort To Fit' item has been added to the SPM/Calibration submenu. This distorts one image such that the positions of four fiducial points match those in a second image. Click on four features in the image to be distorted, then on points corresponding to the same four features in the second image. If the first image is a slice in a stack, then all the slices of the stack will be distorted using the same mapping.
  • Bug fixes:
  • Fixed a bug affecting the loading of TIFF images from SXM manufacturers JEOL, JPK, LEO and Zeiss.
  • Fixed a bug that affected scrolling in save dialogs.
  • Other changes:
  • Modified LEED I-V routines to load TIFF or BMP images rather than QuickTime movies.
  • In Microfibril Analysis, the user can now vary image brightness/contrast during analysis. Also, the algorithm used to find microfibril beads (enhancing contrast, applying an unsharp mask, applying a histogram-dependent threshold) has been refined.
  • When appending a window title with a suffix to indicate the compensation that has been applied (T = Tilt, Q = Quadratic, L = Line-by-Line, etc) the compensation suffix is now inserted before any filename suffix.
  • When duplicating an image the suffix 'copy' or 'copy x' is now inserted before any filename suffix. This is now consistent with way that Finder names duplicated files.
  • Changes to macros:
  • Macro commands 'UpdatesOff' and 'UpdatesOn' have been added to allow user control of window updates. This can result in macro execution speed increases of one or two orders of magnitude if windows are updated very often.

New in Image SXM 194-1X (Jan 24, 2013)

  • Other changes:
  • RHK Technology XPMPro SM4 images now display image types (in the Get Info window) that are more descriptive of the image data.
  • Files with specific suffixes can be now opened by dragging on to the Image SXM icon, regardless of their file type. The file suffixes are:
  • afm, dm2, dm3, dti, ezd, ffr, fits, flt, hdf, hdr, his, ibg, ibw, img, jpk,
  • lsm, mdt, mtrx, nef, opd, pef, pr3, sif, sm2, sm3, sm4, stl, stm, stp,
  • sxm, tb0, tb1, tf0, tf1, tfr, tga, top, wat, xqd, xqf, zfp, zfr, zvi
  • Changes to macros:
  • Two arrays of measurement results (Xi and Yi) have been added to complement the built-in arrays (rX and rY) that hold the XY coordinates of the centres of objects. The new arrays hold the XY coordinates of a point that is guaranteed to be inside the object. (Note that the coordinates held in rX, rY may fall outside the boundary of an object if it has an irregular outline.)

New in Image SXM 193 (Jan 24, 2013)

  • Added features:
  • Support has been added for Leica SP5 confocal microscope LIF images.
  • Support has been added for RHK Technology XPMPro SM4 (v5) images.
  • Support has been added for Veeco Innova SPM images.
  • Support has been added for Zeiss AxioVision images.
  • A new 'Microfibril Analysis' item has been added to the MIASMA menu.
  • Bug fixes:
  • Pasting text could sometimes be disabled.
  • Other changes:
  • Extensive rewrite using Xcode and GNU Pascal Compiler to create Intel-native version.

New in Image SXM 1.93 (Apr 30, 2012)

  • Added features:
  • Support has been added for Leica SP5 confocal microscope LIF images.
  • Support has been added for RHK Technology XPMPro SM4 (v5) images.
  • Support has been added for Veeco Innova SPM images.
  • Support has been added for Zeiss AxioVision images.
  • A new 'Microfibril Analysis' item has been added to the MIASMA menu.
  • Bug fixes:
  • Pasting text could sometimes be disabled.
  • Other changes:
  • Extensive rewrite using Xcode and GNU Pascal Compiler to create Intel-native version.

New in Image SXM 192-1 (Apr 21, 2011)

  • New 'Remove Low Frequencies'.
  • New 'Find Matching Shapes'.
  • New 'Find XY Displacements'.
  • New 'Find Edges (5x5)' filter.
  • Cmd-G will grab a frame from a firewire camera.
  • New 'Bounding Box' added to 'Measurement Options'.
  • Updated support for Molecular Imaging PicoScan v5.3.

New in Image SXM 191-1 (Dec 26, 2010)

  • Added features:
  • A new 'Remove Low Frequencies' item has been added to the FFT submenu. The lowest-frequency discrete components of the FFT are used to determine the low-frequency cutoff. In addition, the highest frequencies are removed to reduce noise.
  • A new 'Find Matching Shapes' item has been added to the Analyze/Specialist Analysis submenu. The user clicks on each of the reference objects in an image and a map is created which colour-codes all the objects that have been matched to one of the reference objects. Pressing the option key allows the user to specify how many reference objects are to be selected. As for the other items in this submenu, effective use of this routine requires some background information.
  • A new 'Find XY Displacements' item has been added to the Analyze/Specialist Analysis submenu. The displacements of molecules relative to a smoothly varying curvilinear grid are displayed as a colour-coded map. As for the other items in this submenu, effective use of this routine requires some background information.
  • A new 'Find Edges (5x5)' filter has been added to the Process menu (using the Option key) and to the Rank Filters dialog box.
  • Bug fixes:
  • When grabbing images from a firewire camera there was a delay of a few seconds (Snow Leopard only).
  • When opening Gatan DigitalMicrograph v3 images, the greyscale is now inverted.
  • Other changes:
  • Colour look-up tables (LUTs) now explicitly set the RGB colours of 0 (white) and 255 (black).
  • New algorithm in 'Parasite Counting Analysis' for greyscale images.
  • 'Lymphocyte Flow Analysis' can now track up to 9999 cells and can handle left-to-right and right-to-left flow.
  • 3-point compensation now works correctly for SPM images with 32-bit image data.
  • When grabbing images from a firewire camera cmd-G will grab a single frame (equivalent to clicking on the 'Grab Frame' button in the 'Capture Control' dialog - the dialog does not need to be open).
  • A new 'Bounding Box' option has been added to the 'Measurement Options' dialog box (for use with 'Measure' and 'Analyze Particles'). The xy position (top left corner) and size (w x h) of the bounding rectangle of the object(s) are displayed in the Info and Results windows.
  • Orientation Imaging is now named 'PrinCIPia'.
  • Updated support for Molecular Imaging PicoScan v5.3 AFM image files.
  • The number of XY coordinates that can be exported has been increased from 32K to 1M.
  • Changes to macros:
  • The macro command 'Filter' has additional options 'HybridMedian' and 'FindEdges5x5' (see above).

New in Image SXM 190-1 (Sep 2, 2010)

  • Added features:
  • The xy coordinates of all objects found in 'Analyze Particles' can be exported.
  • The data in the size/area/height distribution histograms displayed by 'Analyze Results' can be exported.
  • The size/area/height distribution histograms have options for manually setting the bin sizes and ranges. Option-click or double-click on a histogram to change the settings.
  • 'Convolve...' changes to 'Convolve With Gaussian' if an odd-sized square ROI is selected (sigma = size/3).
  • 'Set Scale...' changes to 'Remove XY Scale' if the option key is pressed.
  • 'Calibrate...' changes to 'Remove Z Calibration' if the option key is pressed.
  • Bug fixes:
  • Maximum image sizes are now limited to 16 x 16 Kpix due to limitations of some Carbon code.
  • Scaling with bilinear interpolation for images of width or height > 8 Kpix would give artefacts.
  • Saving an image in a specified file format would apply that as the default format when importing images.
  • Image compensation for JEOL SPM images was not applied correctly.
  • Plot profiles from rectangular ROIs in images with uncalibrated z axes could appear to have calibrated scales.
  • Calculation of a perimeter could give an underestimate by half a pixel depending on the location of the first of the xy coordinates that define the perimeter.
  • Other changes:
  • New algorithm in 'Parasite Counting Analysis' to reduce false negatives and false positives.
  • New algorithm in 'Lymphocyte Flow Analysis' based on Hough transform to improve cell tracking.
  • Updated support for Nanonis SPM images.
  • Convolutions now process all pixels in an image including those at the edges.
  • Paste Control dialog transfer mode popup menu now updates when the transfer mode is changed by a macro.
  • Video grabbing now works for images larger than 800 x 600.
  • Increased the maximum size of a 'marching ants' region from 32 Kpix to 256 Mpix.
  • Increased Info window height to take advantage of larger screen sizes.
  • Pressing 'C' when creating a rectangular/oval selection constrains it to be a centred square/circle.
  • After loading a TIFF stack the window is reset to the first slice.
  • After saving an RGB TIFF image the window is reset to the original colour slice.
  • Autocorrelations and FFTs now behave the same way if a ROI is selected - if the ROI is a power-of-2-sized square then it will be used, otherwise the largest power-of-2-sized square will be selected.
  • Added option in 'Analyze Particles' to stop when the particle count reaches the maximum number of measurements (set in the Measurement Options dialog box). If not selected, when the count reaches the maximum a beep will sound but the particle analysis will continue. See also 'Changes to macros'.
  • Changes to macros:
  • The macro command 'AnalyzeParticles' has an additional option 'StopAtMax' (see above).

New in Image SXM 190 (May 21, 2010)

  • Updated support for Nanonis SPM images. New algorithm in 'Parasite Counting Analysis'. New algorithm in 'Lymphocyte Flow Analysis'. Convolutions now process to the edges. Video grabbing now works for images > 800x600. Scaling images of width > 8000 pixels could give artefacts. Image compensation for JEOL SPM images was not applied correctly. Calculation of a perimeter could give an underestimate by 0.5 pixels.

New in Image SXM 189 (Aug 29, 2009)

  • Added features:
  • A new 'Microcirculation Analysis' item has been added to the Analyze/Specialist Analysis/Cell Analysis submenu. This calculates the speed of red blood cells imaged in videos of sublingual blood vessel networks. As for the other items in this submenu, effective use of this routine requires some background information.
  • A new 'Cornea Cell Analysis' item has been added to the Analyze/Specialist Analysis/Cell Analysis submenu. This calculates the size distribution of corneal cells and the mean, modal and median values.
  • Bug fixes:
  • Omicron Matrix SPM images would sometimes display with a LUT using less than 256 shades of grey.
  • Other changes:
  • The 'Skeletonize' command in the Process/Binary submenu now changes to 'Prune Skeleton' if the option key is pressed. This will prune all branches off a skeleton. See also 'Changes to macros'.
  • 'Show Histogram' changes to 'Show Smoothed Histogram' if the shift key is pressed. Note that the histogram is smoothed, not the image.
  • The 'Cell Analysis' submenu in the Analyze/Specialist Analysis submenu has been renamed 'MIASMA'
  • Changes to macros:
  • The macro command 'PruneSkeleton' has been added (see above).

New in Image SXM 188 (Mar 4, 2009)

  • Fixed NanoScope v5.12 SPM image z calibration issue.
  • Fixed line-by-line compensation bug.
  • Compensation can now be applied to images that are not SPM images.
  • Added background subtraction to 'Particulate Matter Analysis' to compensate for vignetting.

New in Image SXM 187 (Oct 6, 2008)

  • Support has been added for Nanosurf SPM images with both easyScan (.ezd) and Nanosurf Image Document (.nid) file formats.
  • Updated support for RHK Technology XPM Pro SPM images.
  • Recoded some menu handling routines to avoid a crash on PowerMacs running Leopard. Intel macs running Leopard and PowerMacs running Puma/Jaguar/Panther/Tiger were unaffected.
  • Fixed a bug which affected zooming of windows whose width or height was an odd value.
  • Asylum Research SPM images with large footers (> 32 Kb) would not have the correct z calibration.
  • Added options for Omicron SCALA images so that opening a forward (backward) scan image will automatically open the corresponding backward (forward) scan image if the file exists in the same folder. If both images are opened they are displayed as a two–image stack. These options are set in the 'SPM Options' dialog under 'Show Options Specific To: Omicron SCALA'.
  • Added option to 'SXM Options' to use a default colour look-up table (LUT) for every image. To set the default LUT, select the LUT from Options/Color Tables and then save the preferences file from File/Record Preferences or SXM Preferences. If this option is not selected then the image will be displayed with the LUT saved in the file or, if there isn't one, with the current LUT (note that in the latter case this can give odd results with PICT images).
  • Added option to 'SXM Options' to use a default preset spatial calibration for every image. The default scale is selected from a popup menu, which displays the same presets as the Analyze/Preset Scale submenu. If selected, the preset scale will override any spatial calibration defined for the image, so use only if you are sure that you want a fixed spatial scale.
  • Colour LUTs can now be selected by pressing the caps lock key and tabbing (or shift-tabbing) between LUTs.
  • Changes to 'Parasite Counting Analysis' to improve the calculation of the multiplicity of touching parasites and the handling of structured background in images of parasites with no cells.
  • Reinstated browsing of selected images (dropped when browsing was modified to use stacks in v1.85). Option-click to deselect an image. Press the option key and select 'Browse Selected Images' from the File or SEM or SPM/Files menus to redisplay a browse window without the deselected images.
  • After browsing a folder, and optionally deselecting some images by option-clicking, the images can be opened by pressing shift and selecting 'Open Browsed Images' from the File or SEM or SPM/Files menus. If all the images are the same size, they will be opened as a stack. Otherwise they will open in separate windows, as if the user had double-clicked on each thumbnail.
  • When nudging a rectangular region of interest (ROI) using the cursor keys, or stretching it using option-cursor keys, the coordinates of the corners and the width and height are displayed in the Info window.

New in Image SXM 186 (Apr 22, 2008)

  • Limited support has been added for Omicron Matrix STM images.
  • Omicron (pre-SCALA) STM images listed with SPM/Parameters/List Params...
  • Options when browing Omicron SCALA images to display only channel 0 and/or only forward scan.
  • Fixed bug that stopped macro command 'DepthOfFocus' working.

New in Image SXM 185 (Jan 18, 2008)

  • Support for Nanonis SPM images.
  • Support for Asylum Research MFP-3D AFM images.
  • Maximum image size 32000 x 32000 pixels.
  • Maximum number of measurements 99999.
  • Browsing displays thumbnails in a stack.
  • Macro command 'DepthOfFocus' now has arguments.