Full 1
SCANNING SOLutions
TissueFAXS Imaging Software
Full 1

TissueFAXS Imaging Software
Walk-away automation

TissueFAXS is TGs software for the control of the TissueFAXS and TissueFAXS i systems. It provides automated scanning capabilities, a state of the art sample viewer and management of the scan projects.

There are configurations of TissueFAXS for scanning slides, microtiter plates and high-throughput (Slide Loader, 120 slides).

TissueFAXS software is not available as a standalone version or for the control of other microscopes (upgrades of eligible microscopes to TissueFAXS or TissueFAXS S configuration excepted).

TissueFAXS Imaging Software
is integrated into all TG systems

  • TissueFAXS SL
  • TissueFAXS SL PLUS
  • TissueFAXS Spectra
  • TissueFAXS Q
  • TissueFAXS PLUS
  • TissueFAXS Fluo
  • TissueFAXS Histo
  • TissueFAXS i PLUS
  • TissueFAXS i Fluo
  • TissueFAXS i Histo

 

TissueFAXS Workflow and Automation

TissueFAXS workflow is based on a "preview scan - tissue or region detection - high magnification scan" approach. Once a solution has been established for a specific batch of slides a profile containing all essential information for scanning this batch of slides can immediately be saved and reused. The profile can very easily be adapted to divergences in the batch. 

Scan Flow Chart

TissueFAXS GUI

The TissueFAXS GUI is well organised with tabs and static windows.The Camera and Acquired Images tabs as well as the Preview window can be deployed to become discrete windows, with the camera window usually being deployed to the right screen in the two screen computer setups preferred by TG.

The image on the right shows the standard TissueFAXS GUI with the camera window integrated and visible as a tab behind the sample viewer.

 

TissueFAXS GUI

Leishmaniasis parasite detection in cell culture and tissue: Leishmaniasis APP

Leishmania donovani parasites are the causative agents of zoonotic and anthroponotic visceral leishmaniasis. There is no prophylactic vaccine and available drugs are either expensive and/or show significant toxicity, making the research on leishmania biology essential for a detailed understanding of the dispersal of these obligatory-intracellular parasites and their host phagocytes in the skin [1].

The Leishmaniasis APP within TissueGnostics contextual image analysis software, StrataQuest, was designed to assist in immunology research into Leishmaniasis and can be adapted for research on other intracellular parasites. It can be used both on cell cultures and tissue sections. Its main function is to automatically detect parasite stages in cell compartments and quantify them in context with specific immune markers. In this case study, we will show in detail how simple and straightforward the analysis is.

The aim of this project was to detect how many cells are infected by leishmaniasis and the number of leishmaniasis parasites per cell.

The image below shows a mouse skin-draining lymph node stained with DAPI (nucleus, blue).

 IF_Tumor_Foci_Angio_overview-min.png

Nuclei detection based on DAPI staining is one of the most crucial first steps in image analysis; (a) here nuclei are outlined in green. Starting from this, the software defines the whole cell around the nuclei, outlined in yellow for representation (b); (c) detection of parasites inside the cell as shown here as pink dots; (d) combined masks showing cells in yellow and Leishmaniasis parasites in pink.

IF_Tumor_Foci_Angio_panel-min.png

The obtained data is visualized within StrataQuest using scattergrams. In the example below, (e) cells containing parasites are highlighted in red by selecting them in the proper scattergram (in this case, parasites count vs cell size). The individual cells within an image can be chosen and their exact position in the corresponding scattergram is shown – this is a feature available in StrataQuest called forward connection, especially useful for validation of the selected gates.

IF_Tumor_Foci_Angio_scattergram.png

In the end, all results with many parameters to choose from can be outputted into common file formats (Excel, PDF, CSV) for further statistical analysis.

However, the power of StrataQuest´s App-based streamlined workflow does not end with cell/parasite detection. For further deciphering of Leishmania life cycle aspects and distribution processes, the parasite load and the status of parasite stages, e.g. “live/dead” can also be evaluated to obtain additive information. The IF Dots APP enables the analysis of FISH-stained leishmaniasis parasites.

A recent paper utilizing StrataQuest´s analysis software showed that programmed death-ligand 1 (PD-L1) expression is predictive of clinical response to treatment in patients with leishmaniasis [2]. If you are interested in performing detailed context-based quantitative analysis, explore the potential of StrataQuest and StrataQuest Apps.

 

Sources:

  1. Doehl JSP, Ashwin H, Brown N, Romano A, Carmichael S, Pitchford JW, Kaye PM. Spatial Point Pattern Analysis Identifies Mechanisms Shaping the Skin Parasite Landscape in Leishmania donovani Infection. Front Immunol. 2021 Dec 16;12:795554. doi: 10.3389/fimmu.2021.795554.
  2. Nidhi S. Dey, Paul M. Kaye, Shalindra Ranasinghe. Early reduction in PD-L1 expression predicts faster treatment response in human cutaneous leishmaniasis. October 5, 2021. J Clin Invest. 2021;131(22):e142765. doi.org/10.1172/JCI142765.
  3. TissueGnostics, 2022. White paper. PD-L1 raises new hope in the treatment of cutaneous leishmaniasis.

Tissue Detection Technology, Autofocus, Image Stitching & Illumination Correction

TissueFAXS software in all configurations provides comprehensive and robust automatic tissue detection. To take into account the wide variety of stainings and staining quality as well as the placement and size of tissue sections on the slide the algorithm providing tissue detection has controls for adaptation if needed. There are also drawing tools to add to or subtract from the automatic result to further fine tune. If the user does not need an automatic detection of the whole tissue and prefers to identify specific parts of the tissue visually there also are comprehensive drawing tools to set such regions up for scanning.

Tissue Detection 2017

TissueFAXS systems operate with software autofocus. There are two methods, the focal plane or a defined area with one focus point. The focal plane method has the advantage of having smoother focus transitions between its focal points. The graphic on the right illustrates the focal plane with a simplified virtual overlay. The focal points are shown as small flags. TissueFAXS software also stitches the single field of view images of a sample into a seamless digital slide which is visualised in the softwares. Illumination correction (also known as "vignetting" or "flat field" correction) is available both in brightfield and in fluorescence modes.

TissueFAXS scanning speed

TissueFAXS scanning speed is high for automated microscopy. This is supported on the hardware side by cost-efficient, good quality, fast cameras with large sensors, corresponding llumination systems and SSD drives to rapidly store the images. The TissueFAXS software is permanently optimized to integrate these often changing hardware devices.

The images below exemplify scanning speeds in brightfield and epifluorescence. 

1cm2 fluo        1cm2 fluo

 

Tissue Microarray Imaging

TissueFAXS provides a specialised version of the Tissue Detection algorithm for Tissue Microarray (TMA) scanning. This algorithm recognises TMA blocks on the TMA slide provided that the alleys between the blocks are large enough. Within each recognised TMA block the algorithm also recognises the logical block structure, i.e. how many rows and columns there are in the block. Based on this the algorithm puts placeholders core markers for missing or damaged cores into the block detection. These crosshatched markers will not be scanned, they only serve to keep the nomenclature of the cores intact. Blocks can be moved as a whole, scaled in the x and y axes and rotated. Core markers can be moved and resized either individually, in selected groups or for the whole block.

The images below show some of these operations.

 resize tma cores      resize tma cores     resize tma cores

 

DAPI 3 layers

Z-STACKING & FISH IMAGING 

TissueFAXS also offers Extended Focus scanning (also known as focus stacking, focal plane merging, z-stacking or focus blending) and z-stacks. In this method, a series of images above and/or below the actual focal plane of each field of view are scanned in addition. For each image or channel image this "image stack" is then compressed into one image containing all the areas in focus of the whole image stack, resulting in an optimal image.

This method is e.g. essential for FISH analysis as it ensures that no FISH probe above and beneath the actual focal plane is missed. The z-stack images can optionally be saved to be used in 3D reconstruction. 

 

Cell Culture Vessel Imaging

TissueFAXS also has a dedicated scanning mode for microtiter plates. The most commonly used plate types are stored as templates in the software and can be activated as required. The well regions are then automatically established in the right place for scanning (first image shown below). There also is an inbuilt editor for creating more microtiter plate templates. The well regions are also automatically named. Whole well areas or groups thereof can be resized and moved. There is also an option to draw subregions in a well region (rectangular, spherical or polygonal)  and then propagate these into all or a selection of the other well regions. The well regions or their subregions can be scanned and the scans results can then be passed on to TG analysis software to be analysed.

Whole well analysis        Whole well analysis        Whole well analysis

 

High-throughput

TissueFAXS software is also used to scan with the TissueFAXS SL high throughput system in a special configuration allowing the control and management of the 60 two-slide frames (in total 120 slides) in the magazine of the system.

  

Contact

TissueGnostics GmbH
Taborstraße 10/2/8
1020 Vienna, Austria
+43 1 216 11 90
This email address is being protected from spambots. You need JavaScript enabled to view it.

We use cookies on our website. Some of them are essential for the operation of the site, while others help us to improve this site and the user experience (tracking cookies).
You can decide for yourself whether you want to allow cookies or not. Please note that if you reject them, you may not be able to use all the functionalities of the site.