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HISTOquest
Brightfield TISSUE CYTOMETRY
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HistoQuest
single-cell analysis

HistoQuest provides four analysis modes:

  • Cell-based (nucleus, cytoplasm, membrane)
  • Stained areas
  • Small dots (e.g. CISH)
  • Skeleton algorithm for membrane staining

Context-based analysis can be done by manually drawing regions-of-interest. TMAs can be analysed and detected on imported files.

HistoQuest - Features

  • Brightfield image analysis
  • Streamlined workflow
  • Single cell analysis
  • Color separation via spectral unmixing
  • Analyze all types of IHC/HC stainings
  • Analyze tissue sections, TMAs, confluent cells, smears
  • Contextual image analysis by manual ROI definition
  • Nuclear segmentation, total area measurements, dot detection
  • Cytoplasmic and membrane measurements
  • 18 measured metrics per marker
  • Image and data comparison tools

HistoQuest is also available as a standalone software.

HistoQuest 7.1
THE EASY SOLUTION FOR BRIGHTFIELD ANALYSIS

HistoQuest is a brightfield image analysis software for the FACS-like analysis of tissue sections, TMA or cultured cells processed with immunohistochemical or histochemical stains.

HistoQuest

NEW FEATURES in HistoQuest 7.0 & 7.1

The new features of HistoQuest 7 include improvements to the analysis workflow, management of multiple diagrams, image visualization, and the user interface. Here are some highlights of 7.0 & 7.1:

  • 7.1 Nuclear Segmentation using deep learning. It is a particularly useful and simple solution for nuclear segmentation in tissues with extremely high cellular density, weak signal intensity, or high variation in nuclei size and texture.

  • 7.1 Comments from TissueFAXS (slides, regions), including a section for patient information and patient number are available in HistoQuest.

  • 7.1 Export results and analysis masks as BigTiff.

  • 7.1 View diagrams from Statistics Report by double clicking on the result.

  • 7.1 Batch import is now also available for external import sources.

  • 7.0 The new diagrams viewer displays all diagrams associated with a region or sample and allows the user to perform several new tasks, including changing the order of the diagrams via drag and drop, a print preview of the diagrams, set cut-offs, add gates, or show backward connections in the image.

  • 7.0 To further simplify the validation process it is now possible to open multiple samples or regions simultaneously in separate detail windows as well as their raw data, diagram details and diagrams viewer. A dedicated Detail Manager helps to stay organized.

  • 7.0 comes with the new smoothen image function, for visual improvement of the image and new import formats including OME-TIFF, Olympus VSI, BigTIFF and PreciPoint

  • 7.0 Another new feature is the introduction of the Human Protein Atlas Browser within our HistoQuest software. By simply pressing the Human Protein Atlas Button compare your obtained results to publicly available data.

 

DetailManager

IF Dots App: Analysis of FISH

Fluorescence in situ hybridization (FISH) has been routinely used for decades in research and clinics to rapidly identify potential genetical changes within cells. This case study shows how TissueGnostics’ image analysis solution StrataQuest can be applied to evaluate FISH stainings.  The most streamlined solution, the IF Dots App (runs within StrataQuest), can be applied to any analysis of dot-sized objects within the nuclei. Depending on the research needs, the following analysis can be combined with any other kind of analysis including AI-based tissue classification, phenotyping, spatial analysis, etc.

The aim of the following case study was to (i) identify individual nuclei and (ii) to assess how many FISH dots per individual nuclei are present.

The image below shows an overview of a triple staining: the nucleus stained by DAPI (blue), and two FISH markers, the housekeeping gene (green), and HER2/neu (red).

IF Dots original 95

The automated analysis starts with nuclei segmentation (a), where nuclei are identified by the intensity of the DAPI staining (nuclei are marked by the green outline). In the next step, the FISH dots are detected: in red the housekeeping gene in FITC channel (b) and in yellow for the HER2/neu in Acridine channel (c). Then these masks can be combined, as seen in (d).

 

IF Dots min

For further visualization of the analysis results, StrataQuest outputs the data in scattergrams. In the example below, the number of Acridine dots per nucleus (y-axis) is plotted against the FITC dots per nucleus (x-axis). The identified nuclei were gated for the condition “2 acridine dots per nuclei”, where the number of FITC dots can vary, and selected cells are shown in red contour via backward connection. Scattergrams showing the number of detected nuclei with each dot number combination are useful, especially with the Heat Map function enabled (bottom) which indicates those groups with a higher quantity of nuclei. To gain quantitative data for statistical analysis, the results can be immediately exported to Excel, CSV, and PDF formats.

 

IF Dots 2 min

FISH analysis is only one example of StrataQuest´s capabilities. If you are interested in how StrataQuest streamlined image analysis solution can enhance your research today, please reach out to a TissueGnostics team member for a demonstration.

Get to know more about FISH applications combined with TissueGnostics solutions in our blog posts:

HistoQuest analysis automation

HistoQuests fully automated template-based analysis is optimised for clinical routine and research applications and allows complete walk away operation.

The user just has to load samples into the software and to decide whether they want the samples to beautomatically detected (in which case analysis will start immediately), whether they want to be able to interfere with the automatic region detection (with validation) or whether they want to manually define regions-of.interest.

 

A template provides:

  • Segmentation settings for all objects to be detected
  • A method for dealing with events in ROI
  • Markers
  • Diagrams from the first sample of the project from which the template was saved
  • Statistics report settings
  • Simple report settings
  • Small dots settings 

 

 

HistoQuest image analysis algorithms

HistoQuest AlgorithmBrightfield images need to be separated into images according to their color components, HistoQuest provides two algorithms for color separation. 

The first one automatically detects and separates two colors and an optional third one. The second color separation algorithm is semi-manual (using a color picker) and separates an unlimited amount of colors with great control and precision.

HistoQuest uses algorithms for nuclear and cell compartment segmentation. It also provides an algorithm for stained area detection as well as algorithms for the detection of dots inside of already detected cell compartments.

 

 

Nuc-and-Cyto-Segm

The nuclear segmentation algorithm is highly efficient in difficult situations in tissue and can be set with two values only - mean nuclear size and nuclear channel background threshhold. The cell compartment algorithm provides a large amount of flexibility with a few simple settings (yellow outline = segmented nuclei, blue outline = nuclei positive for DAB or cytoplasm positive for Permanent Red marker). The total area algorithm segments stained areas in a sample.

 

 The dot algorithm provides small dot detection ideal for CISH, ISH and other applications in which the quantification of small objects within cellular compartments is needed. The images below show the quantification of EGFR RNA dots inside of the nuclear compartment. Simple context-based analysis can easily be done in HistoQuest by using manual region tools. Drawing the regions takes a negligible amount of time and provides data for epithelial areas and stroma separately in this example. The skeleton algorithm permits the detection of membrane stainings.

quantification of FITC and Texas Red FISH dots inside of the nuclear compartment.

 

TISSUE MICROARRAY
Analysis Support

HistoQuest fully supports the analysis of Tissue Microarrays (TMA) scanned either with TissueFAXS systems or those slide scanners for which HistoQuest provides importers. For analysis projects of scans coming from TissueFAXS systems the autodetected TMA regions will be imported. For scans imported from other scanning systems without detected regions the TMA autodetection feature is also available in HistoQuest.

microarray

CAPABILITIES

 HistoQuest 7.1TissueQuest 7.1 StrataQuest 7.1
Available as a standalone software
Analyze tissue sections, TMAs, confluent cells, smears
Flourescence image analysis  
Brightfield image analysis  
Single cell analysis, total area measurements, dot detection (FISH, CISH, RNAScope), cytoplasmatic and membrane measurements
Contextual image analysis by manual ROI definition
Deep-learning nuclear segmentation
Machine-learning tissue classifier, metastructure detection, automated contextual tissue cytometry, proximity & distance measurements, Spatial relationships & tissue microenvironment analysis    
Highly customizable analysis development    
Apps with predefined analysis solutions    
Analysis of confocal/multispectral and time-lapse projects    

PROPERTIES

  
Operating System Windows 10 System
Platform compatibility TissueFAXS platform (.sqproj), StrataFAXS II (.vmic), Precipoint (.vmic, .gtif), OME-Tiff, Generic Big Tiff, Images (.jpeg, .tif, .bmp, .png), 3D Histech (.mrxs), Hamamatsu (.ndpi), Zeiss Axio Scan (.czi), Yokogawa, Aperio (.svs), Leica (.scn), Keyence, Perkin Elmer (.qptiff)
Export file compatibility Matlab, Python, ImageJ, FIJI, FCS express, most external command line engines

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.

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