How to measure single-cell texture ----------------------------------- This guide shows you how to measure :term:`Haralick Texture Features` on a per-cell basis. Reference keys: :term:`texture`, :term:`single-cell measurement` **Prerequisite:** You must have segmented the cells. Tracking is recommended but not required. Enable :term:`Haralick Texture Features` ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ #. Open the **Measure** tab for your population of interest. #. In the measurement settings, check the **Haralick** option. Configure the parameters ~~~~~~~~~~~~~~~~~~~~~~~~~ #. **Channel**: Select the channel to analyze (e.g., a DNA/DAPI channel for chromatin texture). #. **Distance**: Set the pixel distance for the gray-level co-occurrence matrix computation (default: ``1``). Larger values capture coarser texture patterns. #. **Gray levels**: Set the number of quantized gray-level bins (default: ``256``). Lowering this value (e.g., ``64``) significantly speeds up computation at the cost of intensity resolution. #. **Scale**: Set a downscaling factor between ``0`` and ``1`` to reduce cell crop size before GLCM computation. Useful for large cells. #. **Normalization**: Choose how to normalize intensities before quantization: * **Percentile mode**: clip intensities between a min and max percentile (e.g., 0.01% – 99.9%). * **Absolute mode**: clip between fixed pixel intensity values. .. figure:: ../../_static/texture-measurements.png :align: center :alt: texture_options Run the measurements ~~~~~~~~~~~~~~~~~~~~ #. Click **Set** to save the configuration. #. In the control panel, check the **MEASURE** box and click **Submit**. The following :term:`Haralick Texture Features` will be appended to your measurement table: ``haralick_contrast``, ``haralick_dissimilarity``, ``haralick_homogeneity``, ``haralick_energy``, ``haralick_correlation``, ``haralick_ASM``. .. note:: :term:`Haralick Texture Features` are computationally expensive. Consider lowering the gray levels or using a scale factor < 1 for large datasets.