Quality metrics for automatic evaluation of dual ish images
US-2017323431-A1 · Nov 9, 2017 · US
US11568657B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11568657-B2 |
| Application number | US-202016892075-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 3, 2020 |
| Priority date | Dec 6, 2017 |
| Publication date | Jan 31, 2023 |
| Grant date | Jan 31, 2023 |
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The present disclosure is directed, among other things, to automated systems and methods for analyzing, storing, and/or retrieving information associated with biological objects having irregular shapes. In some embodiments, the systems and methods partition an input image into a plurality of sub-regions based on localized colors, textures, and/or intensities in the input image, wherein each sub-region represents biologically meaningful data.
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The invention claimed is: 1. A system for deriving data corresponding to irregularly-shaped cells from an image of a biological sample comprising at least one stain, the system comprising: (i) one or more processors, and (ii) a memory coupled to the one or more processors, the memory to store computer-executable instructions that, when executed by the one or more processors, cause the system to perform operations comprising: (a) deriving one or more feature metrics from the image; (b) generating a plurality of sub-regions within the image, each sub-region having pixels with similar characteristics, the characteristics selected from color, brightness, and/or texture; (c) computing a series of representational objects that correspond to a set of sub-regions of the generated plurality of sub-regions; wherein: each representational object of the series of representational objects (i) identifies a particular cell type, and (ii) defines an outline of a corresponding sub-region of the set of sub-regions; and each sub-region of the set of sub-regions identifies an amount of stain that exceeds a threshold value; and (d) associating the derived one or more feature metrics from the image with calculated coordinates of each of the series of representational objects. 2. The system of claim 1 , wherein generating plurality of sub-regions comprises deriving superpixels. 3. The system of claim 2 , wherein the superpixels are derived using one of a graph-based approach or a gradient-ascent-based approach. 4. The system of claim 2 , wherein the superpixels are derived by (i) grouping pixels with local k-means clustering; and (ii) using a connected components algorithm to merge small isolated regions into nearest large superpixels. 5. The system of claim 1 , wherein the particular cell type includes a fibroblast or a macrophage. 6. The system of claim 1 , wherein each representational object of the series of representational objects is further identified by a corresponding seed point. 7. The system of claim 1 , wherein the operations further comprise storing the derived one or more feature metrics and associated calculated representational object coordinates in a database. 8. The system of claim 1 , wherein the one or more derived feature metrics comprise at least one expression score selected from percent positivity, an H-score, and a staining intensity. 9. The system of claim 1 , wherein data corresponding to irregularly-shaped cells is derived for a region-of-interest within the image. 10. The system of claim 9 , wherein the region-of-interest is an area of the image annotated by a medical professional. 11. A non-transitory computer-readable medium storing instructions for analyzing data associated with biological objects having irregular shapes, the instructions comprising: (a) instructions for deriving one or more feature metrics from an image of a biological sample, the biological sample comprising at least one stain; (b) instructions for partitioning the image into a series of sub-regions by grouping pixels having similar characteristics, the characteristics selected from color, brightness, and/or texture; (c) instructions for computing a plurality of representational objects that correspond to a set of sub-regions of the series of sub-regions; each representational object of the plurality of representational objects (i) identifies a particular cell type, and (ii) defines an outline of a corresponding sub-region of the set of sub-regions; and each sub-region of the set of sub-regions identifies an amount of stain that exceeds a threshold value; and (d) instructions for associating the derived one or more feature metrics from the image with calculated coordinates of each of the plurality of representational objects. 12. The non-transitory computer-readable medium of claim 11 , wherein the partitioning of the image into the series of sub-regions comprises computing superpixels. 13. The non-transitory computer-readable medium of claim 12 , wherein the superpixels are computed using one of a normalized cuts algorithm, an agglomerative clustering algorithm, a quick shift algorithm, a turbopixel algorithm, or simple linear iterative clustering algorithm. 14. The non-transitory computer-readable medium of claim 12 , wherein the superpixels are generated using simple iterative clustering, and wherein a superpixel size parameter is set to between 40 pixels and 400 pixels, and wherein a compactness parameter is set to between 10 to 100. 15. The non-transitory computer-readable medium of claim 12 , wherein the superpixels are computed by (i) grouping pixels with local k-means clustering; and (ii) using a connected components algorithm to merge small isolated regions into nearest large superpixels. 16. The non-transitory computer-readable medium of claim 11 , wherein the biological sample is stained with at least FAP, and wherein the derived one or more feature metrics include at least one of a FAP staining intensity or a FAP percent positivity. 17. The non-transitory computer-readable medium of claim 16 , wherein an average FAP percent positivity is calculated for all pixels within a sub-region. 18. The non-transitory computer-readable medium of claim 16 , wherein an average FAP staining intensity is calculated for all pixels within a sub-region. 19. The non-transitory computer-readable medium of claim 11 , wherein each representational object of the plurality of representational objects is further identified by a corresponding seed point. 20. The non-transitory computer-readable medium of claim 11 , further comprising instructions for storing the derived one or more feature metrics and associated calculated representational object coordinates in a database. 21. The non-transitory computer-readable medium of claim 20 , further comprising instructions for projecting stored information onto the image of the biological sample.
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