Morphological features from images and masks made easy.
cp_measure: Morphological features for imaging data
Do you need to use CellProfiler features, but you want to do it in a programmatic way? Look no more, this package was developed by and for the click-a-phobic scientists.
Preprint
Here is the preprint. Published as a workshop paper for ICML 2025's CODEML.
Please cite using the following .bib entry
@article{munoz2025cpmeasure,
title={cp\_measure: API-first feature extraction for image-based profiling workflows},
author={Mu{\~n}oz, Al{\'a}n F and Treis, Tim and Kalinin, Alexandr A and Dasgupta, Shatavisha and Theis, Fabian and Carpenter, Anne E and Singh, Shantanu},
journal={arXiv preprint arXiv:2507.01163},
year={2025}
}
Quick overview
Installation
pip install cp-measure
Usage
We provide three entry points: (Featurizer) We orchestrate the images x combinations, (Bulk API) we give you all features and you orchestrate, and (Low-level) you directly import the functions.
Featurizer (Recommended for small datasets)
The simplest way to extract all features from an image and its masks:
import numpy as np
from cp_measure.featurizer import featurize
image: (C, H, W) float array, masks: (N_masks, H, W) integer labels
image = np.random.default_rng(42).random((2, 240, 240))
masks = np.zeros((1, 240, 240), dtype=np.int32)
masks[0, 50:100, 50:100] = 1
masks[0, 150:200, 150:200] = 2
data, columns, rows = featurize(image, masks)
data: np.ndarray of shape (nobjects, nfeatures)
columns: feature names (e.g. "Area", "IntensityMeanIntensity_ch0", ...)
rows: [(None, "object", 1), (None, "object", 2)] — (imageid, objectname, label) per row
To customise which features are extracted, or to name your channels and masks, use makefeaturizerconfig. Channel names are matched positionally to the image's first axis and control how per-channel features are labeled in the output columns (e.g. "IntensityMeanIntensity_DNA"). If omitted, channels are auto-named ch0, ch1, ...
import numpy as np
from cpmeasure.featurizer import featurize, makefeaturizer_config
Recreate variables from previous examples for this block to run in isolation
image = np.random.default_rng(42).random((2, 240, 240))
masks = np.zeros((1, 240, 240), dtype=np.int32)
masks[0, 50:100, 50:100] = 1
masks[0, 150:200, 150:200] = 2
Disable texture features, name channels explicitly
config = makefeaturizerconfig(["DNA", "ER"], texture=False)
data, columns, rows = featurize(image, masks, config)
Multiple mask types (e.g. nuclei and cells) are supported by stacking them along the first axis:
import numpy as np
from cpmeasure.featurizer import featurize, makefeaturizer_config
Recreate variables from previous examples for this block to run in isolation
image = np.random.default_rng(42).random((2, 240, 240))
config = makefeaturizerconfig(["DNA", "ER"], objects=["nuclei", "cells"])
masks = np.zeros((2, 240, 240), dtype=np.int32) masks[0, 50:100, 50:100] = 1 # nucleus 1 masks[1, 40:110, 40:110] = 1 # cell 1 masks[1, 150:200, 150:200] = 2 # cell 2 masks[1, 175:180, 180:210] = 2 # Minor asymmetries on bottom right edge of cells
data, columns, rows = featurize(image, masks, config)
rows: [(None, "nuclei", 1), (None, "cells", 1), (None, "cells", 2)]
Volumetric (C, Z, H, W) data is supported. The featurizer automatically skips 2D-only features (radialdistribution, radialzernikes, zernike, feret). All other features (intensity, sizeshape, texture, granularity, correlations) work for both 2D and 3D.
The output is plain numpy + lists, so converting to a DataFrame is straightforward:
notest
import pandas as pd
row_names = [f"{img}{obj}{label}" for img, obj, label in rows]
df = pd.DataFrame(data, index=row_names, columns=columns)
Note: DataFrame libraries must be installed independently, to keep the dependency tree low.
Bulk API (Access all measurements at once)
For more control over individual measurements, or to call specific functions directly, use the bulk API. It operates on single images and masks following the scikit-image convention.
cp_measure currently provides two types of measurements based on their inputs:
- Type 1: 1 image + 1 set of masks (e.g., intensity)
- Type 2: 2 images + 1 set of masks (e.g., colocalization)
import numpy as np
from cpmeasure.bulk import getcore_measurements
measurements = getcoremeasurements()
print(measurements.keys())
dictkeys(['radialdistribution', 'radial_zernikes', 'intensity', 'sizeshape', 'zernike', 'feret', 'texture', 'granularity'])
Create synthetic data
size = 240
rng = np.random.default_rng(42)
pixels = rng.integers(low=1, high=255, size=(size, size))
Create two similar-sized objects
masks = np.zeros_like(pixels)
masks[50:100, 50:100] = 1
masks[150:200, 150:200] = 2
measurements = getcoremeasurements() results = {} for name, func in measurements.items(): results = {results, func(masks, pixels)}
""" {'RadialDistributionFracAtD1of4': array([0.03673493, 0.05640786]), 'RadialDistributionMeanFrac1of4': array([1.02857809, 1.15072037]), 'RadialDistributionRadialCV1of4': array([0.05539421, 0.04635982]), ... 'Granularity_16': array([97.65759629, 97.64371833]) } """
Low-level access
Individual measurement functions can be imported directly. Each returns a dictionary of arrays.
import numpy as np
from cpmeasure.core.measureobjectsizeshape import getsizeshape
mask = np.zeros((50, 50), dtype=np.int32) mask[5:-6, 5:-6] = 1 get_sizeshape(mask, None)
measureobjectintensitydistribution.getradialzernikes
measureobjectintensity.get_intensity
measureobjectsizeshape.get_zernike
measureobjectsizeshape.get_feret
measuregranularity.get_granularity
measuretexture.get_texture
measurecolocalization.getcorrelationpearson
measurecolocalization.getcorrelationmanders_fold
measurecolocalization.getcorrelationrwc
measurecolocalization.getcorrelationcostes
measurecolocalization.getcorrelationoverlap
Important notes
- Labels: Any positive integer labels work — non-contiguous IDs (e.g.
[1, 3, 4]) are relabelled to1..Ninternally without modifying your array, and results are reported against your original IDs.featurizeand the bulkget*registries sanitize by default (sanitize=Falseto opt out); raw measurement functions assume contiguous1..N, so wrap them withcpmeasure._sanitize.sanitizeif you call them directly with gapped IDs. - Fidelity: If you need to match CellProfiler measurements 1:1, you must convert your image arrays to float values between 0 and 1. For instance, if you have an array of data type uint16, you must divide them all by 65535. This is important for radial distribution measurements. For the four intensity quantile features (
LowerQuartileIntensity,MedianIntensity,UpperQuartileIntensity,MADIntensity) you additionally needlegacy=True— see below. - Speed: The Granularity measurement is particularly slow (~80% of the compute time). Skip this one it if speed is of utmost importance.
- Legacy percentile convention:
getintensity(numpy and numba backends),getcoremeasurements,getcoremeasurements3d, andmakefeaturizerconfigacceptlegacy: bool = False. The default usesnumpy.percentile'linear' ((n-1)q) quartiles and the textbookmedian(|x - median(x)|)MAD. Passlegacy=Trueto reproduce the original cp_measure / CellProfiler behavior:nqquartiles and the(1/ndim)-quantile MAD (which returns the 33rd percentile in 3D rather than the median). All other intensity features are identical either way. - Minor floating-point discrepancy: Some features produce a minor (1e-16) discrepancy when using one vs multiple mask in some features. The issue lies upstream (centrosome, scipy), and does not significantly impact my use-cases.
Similar projects
- spacr: Library to analyse screens, it provides measurements (independent implementation) and a GUI.
- ScaleFEX: Python pipeline that includes measurements, designed for the cloud.
- thyme: Rust library to extract a subset of CellProfiler's features efficiently (independent implementation).
Current work
You can follow progress here.
Most features are implemented, but Type 3 measurements (e.g., ObjectNeighbors) does not have a wrapper. We do not plan to implement ObjectSkeleton.
Contributing
See CONTRIBUTING.md for details.