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A. Three-colour high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against Sec16 (orange) and 𝛽-COP (purple). B. Quantitative data highlighting the relative distribution of COPII (HaloTag-Sec23A) and transitional ER (Sec16A). Left panel: Violin plots of the distance between centroids of endogenous HaloTag-Sec23A puncta from immunostained Sec16 and 𝛽-COP. Extracted from the three-color high resolution confocal fluorescence imaging as exampled in A. For Sec16, n = 5819, from ≥10 cells, across 3 experimental repeats. For 𝛽-COP, n = 4950, from ≥10 cells, across 4 experimental repeats. Right panel: Averaged <t>linescans</t> of Sec16 (orange) and HaloTag-Sec23A (green), extracted from two-colour super resolution STED imaging and fitted from 50 structures across 2 cells over 1 experimental repeat. Standard error is shown by the dotted lines. The intensity values were normalized for display purposes. C. Three-color high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against ERGIC-53 (cyan) and 𝛽-COP (purple). D. Two-colour super resolution STED imaging of endogenous SNAP-tag-ERGIC-53 RPE1 cells stained with antibodies directed against 𝛽-COP (purple) and SNAP-tag-ERGIC-53 dyed with JFX650-SNAP-tag ligand (cyan) Scale bar: A,C overviews: 1 µm, insets: 200 nm, D: 100 nm
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GeoTek Inc geotek linescan camera
A. Three-colour high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against Sec16 (orange) and 𝛽-COP (purple). B. Quantitative data highlighting the relative distribution of COPII (HaloTag-Sec23A) and transitional ER (Sec16A). Left panel: Violin plots of the distance between centroids of endogenous HaloTag-Sec23A puncta from immunostained Sec16 and 𝛽-COP. Extracted from the three-color high resolution confocal fluorescence imaging as exampled in A. For Sec16, n = 5819, from ≥10 cells, across 3 experimental repeats. For 𝛽-COP, n = 4950, from ≥10 cells, across 4 experimental repeats. Right panel: Averaged <t>linescans</t> of Sec16 (orange) and HaloTag-Sec23A (green), extracted from two-colour super resolution STED imaging and fitted from 50 structures across 2 cells over 1 experimental repeat. Standard error is shown by the dotted lines. The intensity values were normalized for display purposes. C. Three-color high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against ERGIC-53 (cyan) and 𝛽-COP (purple). D. Two-colour super resolution STED imaging of endogenous SNAP-tag-ERGIC-53 RPE1 cells stained with antibodies directed against 𝛽-COP (purple) and SNAP-tag-ERGIC-53 dyed with JFX650-SNAP-tag ligand (cyan) Scale bar: A,C overviews: 1 µm, insets: 200 nm, D: 100 nm
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A. Three-colour high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against Sec16 (orange) and 𝛽-COP (purple). B. Quantitative data highlighting the relative distribution of COPII (HaloTag-Sec23A) and transitional ER (Sec16A). Left panel: Violin plots of the distance between centroids of endogenous HaloTag-Sec23A puncta from immunostained Sec16 and 𝛽-COP. Extracted from the three-color high resolution confocal fluorescence imaging as exampled in A. For Sec16, n = 5819, from ≥10 cells, across 3 experimental repeats. For 𝛽-COP, n = 4950, from ≥10 cells, across 4 experimental repeats. Right panel: Averaged <t>linescans</t> of Sec16 (orange) and HaloTag-Sec23A (green), extracted from two-colour super resolution STED imaging and fitted from 50 structures across 2 cells over 1 experimental repeat. Standard error is shown by the dotted lines. The intensity values were normalized for display purposes. C. Three-color high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against ERGIC-53 (cyan) and 𝛽-COP (purple). D. Two-colour super resolution STED imaging of endogenous SNAP-tag-ERGIC-53 RPE1 cells stained with antibodies directed against 𝛽-COP (purple) and SNAP-tag-ERGIC-53 dyed with JFX650-SNAP-tag ligand (cyan) Scale bar: A,C overviews: 1 µm, insets: 200 nm, D: 100 nm
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Schematic of the calibration library procedure followed in the operating room with the simplified 3D model of the SLIMBRAIN prototype 3. ( a ) Illustration of the positioning of the acquisition system with respect to the diffuse reflectance target. ( b ) White and dark references obtained with the Ximea snapshot and Headwall <t>linescan</t> cameras.
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Schematic of the calibration library procedure followed in the operating room with the simplified 3D model of the SLIMBRAIN prototype 3. ( a ) Illustration of the positioning of the acquisition system with respect to the diffuse reflectance target. ( b ) White and dark references obtained with the Ximea snapshot and Headwall <t>linescan</t> cameras.
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Schematic of the calibration library procedure followed in the operating room with the simplified 3D model of the SLIMBRAIN prototype 3. ( a ) Illustration of the positioning of the acquisition system with respect to the diffuse reflectance target. ( b ) White and dark references obtained with the Ximea snapshot and Headwall <t>linescan</t> cameras.
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Headwall Photonics hyperspec® vnir e-series linescan camera
Schematic of the calibration library procedure followed in the operating room with the simplified 3D model of the SLIMBRAIN prototype 3. ( a ) Illustration of the positioning of the acquisition system with respect to the diffuse reflectance target. ( b ) White and dark references obtained with the Ximea snapshot and Headwall <t>linescan</t> cameras.
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Image Search Results


A. Three-colour high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against Sec16 (orange) and 𝛽-COP (purple). B. Quantitative data highlighting the relative distribution of COPII (HaloTag-Sec23A) and transitional ER (Sec16A). Left panel: Violin plots of the distance between centroids of endogenous HaloTag-Sec23A puncta from immunostained Sec16 and 𝛽-COP. Extracted from the three-color high resolution confocal fluorescence imaging as exampled in A. For Sec16, n = 5819, from ≥10 cells, across 3 experimental repeats. For 𝛽-COP, n = 4950, from ≥10 cells, across 4 experimental repeats. Right panel: Averaged linescans of Sec16 (orange) and HaloTag-Sec23A (green), extracted from two-colour super resolution STED imaging and fitted from 50 structures across 2 cells over 1 experimental repeat. Standard error is shown by the dotted lines. The intensity values were normalized for display purposes. C. Three-color high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against ERGIC-53 (cyan) and 𝛽-COP (purple). D. Two-colour super resolution STED imaging of endogenous SNAP-tag-ERGIC-53 RPE1 cells stained with antibodies directed against 𝛽-COP (purple) and SNAP-tag-ERGIC-53 dyed with JFX650-SNAP-tag ligand (cyan) Scale bar: A,C overviews: 1 µm, insets: 200 nm, D: 100 nm

Journal: bioRxiv

Article Title: Multi-scale Molecular Imaging of Human Cells reveals COPI and COPII Vesicles at ER Exit Sites

doi: 10.1101/2025.07.29.667472

Figure Lengend Snippet: A. Three-colour high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against Sec16 (orange) and 𝛽-COP (purple). B. Quantitative data highlighting the relative distribution of COPII (HaloTag-Sec23A) and transitional ER (Sec16A). Left panel: Violin plots of the distance between centroids of endogenous HaloTag-Sec23A puncta from immunostained Sec16 and 𝛽-COP. Extracted from the three-color high resolution confocal fluorescence imaging as exampled in A. For Sec16, n = 5819, from ≥10 cells, across 3 experimental repeats. For 𝛽-COP, n = 4950, from ≥10 cells, across 4 experimental repeats. Right panel: Averaged linescans of Sec16 (orange) and HaloTag-Sec23A (green), extracted from two-colour super resolution STED imaging and fitted from 50 structures across 2 cells over 1 experimental repeat. Standard error is shown by the dotted lines. The intensity values were normalized for display purposes. C. Three-color high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A RPE1 cells dyed with HaloTag JFX650 ligand (green) and stained with antibodies directed against ERGIC-53 (cyan) and 𝛽-COP (purple). D. Two-colour super resolution STED imaging of endogenous SNAP-tag-ERGIC-53 RPE1 cells stained with antibodies directed against 𝛽-COP (purple) and SNAP-tag-ERGIC-53 dyed with JFX650-SNAP-tag ligand (cyan) Scale bar: A,C overviews: 1 µm, insets: 200 nm, D: 100 nm

Article Snippet: To create the linescans, Imaris was used to pick spots at the intended beginning and end of the line of interest.

Techniques: Fluorescence, Imaging, Staining

A. Three-color high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A dyed with HaloTag JFX650 ligand (green) and immunostained Sec12 (purple) and TFG (orange). B. Two-color super resolution STED imaging of endogenous HaloTag-Sec23A dyed with HaloTag JFX650 ligand (green) and immunostained TFG (pink). C. Averaged linescans of TFG (pink) and HaloTag-Sec23A (green) fitted from 50 measurements across 9 cells over 3 experimental repeats, showing the distribution of HaloTag-Sec23A signal from the center of TFG condensates extracted from the two-color super resolution STED imaging. Standard error is shown with by the dotted lines. Scale bars overviews: 1 µm, insets: 100 nm

Journal: bioRxiv

Article Title: Multi-scale Molecular Imaging of Human Cells reveals COPI and COPII Vesicles at ER Exit Sites

doi: 10.1101/2025.07.29.667472

Figure Lengend Snippet: A. Three-color high resolution confocal fluorescence imaging of endogenous HaloTag-Sec23A dyed with HaloTag JFX650 ligand (green) and immunostained Sec12 (purple) and TFG (orange). B. Two-color super resolution STED imaging of endogenous HaloTag-Sec23A dyed with HaloTag JFX650 ligand (green) and immunostained TFG (pink). C. Averaged linescans of TFG (pink) and HaloTag-Sec23A (green) fitted from 50 measurements across 9 cells over 3 experimental repeats, showing the distribution of HaloTag-Sec23A signal from the center of TFG condensates extracted from the two-color super resolution STED imaging. Standard error is shown with by the dotted lines. Scale bars overviews: 1 µm, insets: 100 nm

Article Snippet: To create the linescans, Imaris was used to pick spots at the intended beginning and end of the line of interest.

Techniques: Fluorescence, Imaging

Schematic of the calibration library procedure followed in the operating room with the simplified 3D model of the SLIMBRAIN prototype 3. ( a ) Illustration of the positioning of the acquisition system with respect to the diffuse reflectance target. ( b ) White and dark references obtained with the Ximea snapshot and Headwall linescan cameras.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: Schematic of the calibration library procedure followed in the operating room with the simplified 3D model of the SLIMBRAIN prototype 3. ( a ) Illustration of the positioning of the acquisition system with respect to the diffuse reflectance target. ( b ) White and dark references obtained with the Ximea snapshot and Headwall linescan cameras.

Article Snippet: Ximea linescan , /ID_ x _CN_ y /scan/linescan , ID x LS y .tif , uint8 , 78–106 , Sequence of raw HS images.

Techniques:

Representation of the spatial and spectral information captured in every line with the Headwall linescan HS camera. The information is saved using the BIL binary format with a header file indicating how to read the data.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: Representation of the spatial and spectral information captured in every line with the Headwall linescan HS camera. The information is saved using the BIL binary format with a header file indicating how to read the data.

Article Snippet: Ximea linescan , /ID_ x _CN_ y /scan/linescan , ID x LS y .tif , uint8 , 78–106 , Sequence of raw HS images.

Techniques:

Normalized reflectance spectral responses with correlation values when illuminating the polymer reference with lamps B and D from Fig. and captured with different sensors. Spectrometer measurements were performed with a fibre optic orthogonal to the polymer reference from a 5 cm distance. The hyperspectral camera captures a scene of the polymer at approximately 72.5 degrees and 40.5 cm distance and uses a region of interest of 25 × 25 pixels. Note that captures taken at 90 ∘ and 0 ∘ would mean pointing the camera to a vertical wall and to the floor, respectively. These responses from the HS cameras are the mean spectral signatures of the 25 × 25 pixel polymer pixels with their corresponding standard deviations, shown with shaded colours between their corresponding means. The spectrometer uses 2055 bands and covers the 350–925 nm range. The HS linescan VNIR camera covers the 400–1000 nm spectral range and uses 369 bands. Finally, the HS snapshot NIR camera spectra ranges from 660–950 nm and includes 25 bands. The Pearson correlation is presented after the measured bands of each sensor are compared with the polymer reference response. The visible (VIS) spectra is illustrated with rainbow shading in the 380–740 nm range.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: Normalized reflectance spectral responses with correlation values when illuminating the polymer reference with lamps B and D from Fig. and captured with different sensors. Spectrometer measurements were performed with a fibre optic orthogonal to the polymer reference from a 5 cm distance. The hyperspectral camera captures a scene of the polymer at approximately 72.5 degrees and 40.5 cm distance and uses a region of interest of 25 × 25 pixels. Note that captures taken at 90 ∘ and 0 ∘ would mean pointing the camera to a vertical wall and to the floor, respectively. These responses from the HS cameras are the mean spectral signatures of the 25 × 25 pixel polymer pixels with their corresponding standard deviations, shown with shaded colours between their corresponding means. The spectrometer uses 2055 bands and covers the 350–925 nm range. The HS linescan VNIR camera covers the 400–1000 nm spectral range and uses 369 bands. Finally, the HS snapshot NIR camera spectra ranges from 660–950 nm and includes 25 bands. The Pearson correlation is presented after the measured bands of each sensor are compared with the polymer reference response. The visible (VIS) spectra is illustrated with rainbow shading in the 380–740 nm range.

Article Snippet: Ximea linescan , /ID_ x _CN_ y /scan/linescan , ID x LS y .tif , uint8 , 78–106 , Sequence of raw HS images.

Techniques: Polymer

Raincloud plot with the SAM thresholds used for every reference label pixel. Obtained during the ground-truth labelling procedure for the Headwall linescan brain captures with IDs, which can be found inside the zipped folder “PaperExperiments” on the e-cienciaDatos repository, as well as in the Headwall_Linescan_GT_Patient_IDs.txt file.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: Raincloud plot with the SAM thresholds used for every reference label pixel. Obtained during the ground-truth labelling procedure for the Headwall linescan brain captures with IDs, which can be found inside the zipped folder “PaperExperiments” on the e-cienciaDatos repository, as well as in the Headwall_Linescan_GT_Patient_IDs.txt file.

Article Snippet: Ximea linescan , /ID_ x _CN_ y /scan/linescan , ID x LS y .tif , uint8 , 78–106 , Sequence of raw HS images.

Techniques:

ROC curves obtained on the test set with two RF models trained with labelled pixels from both the snapshot and the linescan HS cameras independently. Each class contains the AUC score in the legend expressed in %.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: ROC curves obtained on the test set with two RF models trained with labelled pixels from both the snapshot and the linescan HS cameras independently. Each class contains the AUC score in the legend expressed in %.

Article Snippet: Ximea linescan , /ID_ x _CN_ y /scan/linescan , ID x LS y .tif , uint8 , 78–106 , Sequence of raw HS images.

Techniques:

Schematic of the calibration library procedure followed in the operating room with the simplified 3D model of the SLIMBRAIN prototype 3. ( a ) Illustration of the positioning of the acquisition system with respect to the diffuse reflectance target. ( b ) White and dark references obtained with the Ximea snapshot and Headwall linescan cameras.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: Schematic of the calibration library procedure followed in the operating room with the simplified 3D model of the SLIMBRAIN prototype 3. ( a ) Illustration of the positioning of the acquisition system with respect to the diffuse reflectance target. ( b ) White and dark references obtained with the Ximea snapshot and Headwall linescan cameras.

Article Snippet: Although three HS cameras have been utilized to acquire images, the images taken from the Ximea linescan camera presented many difficulties when reconstructing HS cubes with the nonflat surface of the brain.

Techniques:

Representation of the spatial and spectral information captured in every line with the Headwall linescan HS camera. The information is saved using the BIL binary format with a header file indicating how to read the data.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: Representation of the spatial and spectral information captured in every line with the Headwall linescan HS camera. The information is saved using the BIL binary format with a header file indicating how to read the data.

Article Snippet: Although three HS cameras have been utilized to acquire images, the images taken from the Ximea linescan camera presented many difficulties when reconstructing HS cubes with the nonflat surface of the brain.

Techniques:

Normalized reflectance spectral responses with correlation values when illuminating the polymer reference with lamps B and D from Fig. and captured with different sensors. Spectrometer measurements were performed with a fibre optic orthogonal to the polymer reference from a 5 cm distance. The hyperspectral camera captures a scene of the polymer at approximately 72.5 degrees and 40.5 cm distance and uses a region of interest of 25 × 25 pixels. Note that captures taken at 90 ∘ and 0 ∘ would mean pointing the camera to a vertical wall and to the floor, respectively. These responses from the HS cameras are the mean spectral signatures of the 25 × 25 pixel polymer pixels with their corresponding standard deviations, shown with shaded colours between their corresponding means. The spectrometer uses 2055 bands and covers the 350–925 nm range. The HS linescan VNIR camera covers the 400–1000 nm spectral range and uses 369 bands. Finally, the HS snapshot NIR camera spectra ranges from 660–950 nm and includes 25 bands. The Pearson correlation is presented after the measured bands of each sensor are compared with the polymer reference response. The visible (VIS) spectra is illustrated with rainbow shading in the 380–740 nm range.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: Normalized reflectance spectral responses with correlation values when illuminating the polymer reference with lamps B and D from Fig. and captured with different sensors. Spectrometer measurements were performed with a fibre optic orthogonal to the polymer reference from a 5 cm distance. The hyperspectral camera captures a scene of the polymer at approximately 72.5 degrees and 40.5 cm distance and uses a region of interest of 25 × 25 pixels. Note that captures taken at 90 ∘ and 0 ∘ would mean pointing the camera to a vertical wall and to the floor, respectively. These responses from the HS cameras are the mean spectral signatures of the 25 × 25 pixel polymer pixels with their corresponding standard deviations, shown with shaded colours between their corresponding means. The spectrometer uses 2055 bands and covers the 350–925 nm range. The HS linescan VNIR camera covers the 400–1000 nm spectral range and uses 369 bands. Finally, the HS snapshot NIR camera spectra ranges from 660–950 nm and includes 25 bands. The Pearson correlation is presented after the measured bands of each sensor are compared with the polymer reference response. The visible (VIS) spectra is illustrated with rainbow shading in the 380–740 nm range.

Article Snippet: Although three HS cameras have been utilized to acquire images, the images taken from the Ximea linescan camera presented many difficulties when reconstructing HS cubes with the nonflat surface of the brain.

Techniques: Polymer

Raincloud plot with the SAM thresholds used for every reference label pixel. Obtained during the ground-truth labelling procedure for the Headwall linescan brain captures with IDs, which can be found inside the zipped folder “PaperExperiments” on the e-cienciaDatos repository, as well as in the Headwall_Linescan_GT_Patient_IDs.txt file.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: Raincloud plot with the SAM thresholds used for every reference label pixel. Obtained during the ground-truth labelling procedure for the Headwall linescan brain captures with IDs, which can be found inside the zipped folder “PaperExperiments” on the e-cienciaDatos repository, as well as in the Headwall_Linescan_GT_Patient_IDs.txt file.

Article Snippet: Although three HS cameras have been utilized to acquire images, the images taken from the Ximea linescan camera presented many difficulties when reconstructing HS cubes with the nonflat surface of the brain.

Techniques:

ROC curves obtained on the test set with two RF models trained with labelled pixels from both the snapshot and the linescan HS cameras independently. Each class contains the AUC score in the legend expressed in %.

Journal: Scientific Data

Article Title: SLIMBRAIN database: A multimodal image database of in vivo human brains for tumour detection

doi: 10.1038/s41597-025-04993-y

Figure Lengend Snippet: ROC curves obtained on the test set with two RF models trained with labelled pixels from both the snapshot and the linescan HS cameras independently. Each class contains the AUC score in the legend expressed in %.

Article Snippet: Although three HS cameras have been utilized to acquire images, the images taken from the Ximea linescan camera presented many difficulties when reconstructing HS cubes with the nonflat surface of the brain.

Techniques: