Keras R-CNN: library for cell detection in biological images using deep neural networks

Abstract

Background

A common yet still manual task in basic biology research, high-throughput drug screening and digital pathology is identifying the number, location, and type of individual cells in images. Object detection methods can be useful for identifying individual cells as well as their phenotype in one step. State-of-the-art deep learning for object detection is poised to improve the accuracy and efficiency of biological image analysis.

Results

We created Keras R-CNN to bring leading computational research to the everyday practice of bioimage analysts. Keras R-CNN implements deep learning object detection techniques using Keras and Tensorflow (https://github.com/broadinstitute/keras-rcnn). We demonstrate the command line tool’s simplified Application Programming Interface on two important biological problems, nucleus detection and malaria stage classification, and show its potential for identifying and classifying a large number of cells. For malaria stage classification, we compare results with expert human annotators and find comparable performance.

Conclusions

Keras R-CNN is a Python package that performs automated cell identification for both brightfield and fluorescence images and can process large image sets. Both the package and image datasets are freely available on GitHub and the Broad Bioimage Benchmark Collection.

Background

Identifying individual cells in images is often a crucial task for basic biology research, high-throughput drug screening and digital pathology. Traditional segmentation methods (Fig. 1a) identify individual pixels that belong to each distinct object through a carefully designed series of image processing steps, often involving watershed, distance transform, and intensity gradients. This approach requires algorithm selection and parameter tuning (and thus time and expertise), is computationally expensive, and often fails to sufficiently handle noisy images, illumination fluctuations, and clumped cells. In cases where phenotype classification is also needed, hundreds of classical morphological features are extracted per cell, followed by a subsequent machine learning step to classify each cell. User-friendly software exists for these steps [1–4], but it does add significant effort to a typical workflow.

Fig. 1.

Overview of a traditional segmentation based pipeline and a deep learning based object detection pipeline. a. Traditional segmentation based pipelines require the selection and tuning of multiple classical image processing algorithms to produce a segmentation, where pixels associated with individual instances (e.g. nuclei, or cells) receive unique “labels”, represented here as different colors. b. Deep learning-based object detection pipelines require some example annotated images to be provided, and use neural networks to learn a model that can produce bounding boxes around each object, which can be overlapping. If multiple object classes are of interest (for example, multiple phenotypes), each bounding box is assigned a class. c. Code to train an object detection model, written using Keras R-CNN’s API. d. Graphs of cell counts of each infected type over time predicted on time course images. The time course set contains samples prepared at particular hours between 0 and 44 h and has been designed to synchronize the parasites’ growth and to show representation of all stages. The ground truth is based on Annotator 1, who annotated all images in the dataset including the training data

Deep learning holds tremendous promise to overcome these challenges by simplifying workflows while also improving accuracy, at least in many contexts [5]. In particular, deep learning-based object detection algorithms (Fig. 1b) examine the raw pixels of images and discover which features and combinations of features best describe each phenotypic class of cells (based on examples provided by the researcher), with minimal user configuration of mathematical parameters. They can conveniently identify cells as well as their phenotype in one step. In contrast to segmentation, object detection algorithms yield a bounding box around each cell. Treating cell identification as an object detection problem rather than a pixel-level segmentation problem has several advantages, most notably that the annotation step is orders of magnitude faster. Drawing bounding boxes (in essence, marking two points in space) is much faster than the pixel level annotation that is needed for ground truth for training segmentation models, and they allow overlapping objects to be easily distinguishable. Object detection algorithms additionally do not need distinct steps to separate overlapping or touching cells and require much less storage in terms of training data and results. For cases where pixel-level segmentation is needed, object detection can be followed by post-processing steps to define precise boundaries for each object.

Here, we present an open source Keras package for cell detection called Keras R-CNN, as well as pre-trained deep learning models and new public datasets. Keras R-CNN is based on the Faster Region-based Convolutional Neural Network (Faster R-CNN) [6] architecture, which is currently the basis of many best-performing models for object detection. It was among the top scoring in the 2018 Data Science Bowl public competition we co-organized [7] and has already compared favorably with other deep learning architectures in performance and inference time [5, 8] (Supplementary Figure S6). Faster R-CNN takes an image as input and generates bounding boxes and bounding box classifications [9]. Training involves gathering appropriate data as ground truth, namely a set of images with known bounding box coordinates and annotated labels annotated. Initially, a training procedure adapts the model to a particular application by optimizing the weights in the network. Subsequently, inference or prediction involves new images running through the trained model to produce output bounding box coordinates and class probabilities. To test the accuracy of a trained model for a given application, prediction is performed on a set of images that were not used for training (and, importantly, were collected in a completely different experimental batch than those used for training [10]). The predictions are compared to the known ground truth annotations to characterize accuracy.

Implementation

Keras R-CNN is distinguished from other deep learning based object detection implementations like Facebook’s Detectron [11] or Tensorflow’s Object Detection API [12] in several ways. First, Keras R-CNN can process an unlimited number of channels. Unlike standard consumer photos’ red, green and blue (RGB) channels, biological imaging assays often involve up to several dozen fluorescent labels in multispectral imaging. The Keras R-CNN schema is designed for users to easily provide their own datasets; its modular structure allows for flexibility and interoperability with Keras and the scientific Python ecosystems including NumPy, and it is portable across platforms (Windows, Mac, Linux) and devices. It also includes dataset augmentation through cropping, rescaling, and rotating; and efficient handling of large scale, densely annotated, and three (or more)-dimensional datasets.

Keras R-CNN can train a model in just a few lines of code as compared to the hundreds or even thousands required by other implementations (Fig. 1c). While not itself a point-and-click tool, Keras R-CNN could serve as the foundation for a more accessible software tool serving biologists and pathologists [13]. The use of Keras offers platform and device portability while being abstract enough for the code to be understandable and easily customizable. We also designed a human-readable schema for datasets (see Supplemental Material), which is readily understood by non-experts in computer vision so they can focus on solving biological problems.

Results

We first demonstrated Keras R-CNN on a very common application: nucleus detection (see Supplementary Figure S1). We used manually annotated fluorescent images showing nuclei stained with Hoechst 33342 to highlight their DNA. The ~ 600 training images (~ 30,000 nuclei) were from the 2018 Data Science Bowl (DSB) dataset BBBC038 and the ~ 100 testing images (~ 10,000 nuclei) were from a subset of the human U2OS cell dataset BBBC022 [14, 15]. We recently described instance segmentation of nuclei [16]; here we instead address the problem of object detection, which yields bounding boxes and whose accuracy is assessed by a different metric.

We found that the trained model achieved a mean average precision score of 82% at an intersection-over-union (IoU) threshold of 0.5. For comparison, we also tested the traditional approach of segmentation, using a CellProfiler [17] pipeline tuned to the data, achieving a score of 81%. The resulting scores are very similar, indicating that, on this relatively straightforward image analysis task, Keras R-CNN can perform as well as classical image processing algorithms that have been parameter-tuned by experts.

We next tested a more complex case: detection of cells in blood smears of patients infected with the human malaria parasite Plasmodium vivax in various stages, which requires phenotype classification (Supplementary Figure 2A) in addition to object detection. P. vivax causes a significant health burden in malaria endemic regions. Manual inspection of blood smears by trained microscopists remains the gold standard of parasite detection and stage determination because of its low cost and high flexibility. However, manual inspection and counting is tedious, requires resources to develop expertise, and is prone to significant human variability as the phenotypic changes are very subtle.

We applied Keras R-CNN to classify different stages of P. vivax development, with particular focus on trophozoites vs gametocytes. We collected 1364 images (~ 80,000 cells) from samples prepared by different groups: from Brazil, from Southeast Asia, and ex-vivo cultured samples prepared as a time course [18] and made them publicly available as BBBC041 (see Supplementary Table S1). We created these three datasets across sites to increase reproducibility and robustness across different sample sets, preventing overfitting to a single laboratory’s imaging and staining routine (Supplementary Figure 2C). We used the time course images as our holdout set, and the others as training data.

We found that a trained Keras R-CNN model achieved a mean average precision score of 78% at an IoU threshold of 0.5 (Supplementary Figure 1), much higher than an expert-configured CellProfiler pipeline, which yielded 61%. Classical image processing struggles with this task, which is much more challenging than nucleus detection because the malaria images are brightfield rather than the high signal-to-noise fluorescent images in the nucleus detection case.

Because Keras R-CNN learns from expert-provided data, it is able to handle different image modalities without hand tuning parameters.

Mean average precision only assesses the ability to locate cells; we also evaluated phenotype classification. Classifying P. vivax stages is notoriously difficult, and often experts disagree. We quantified the level and nature of disagreement by giving two expert annotators the same set of blood smear images; there is significant confusion (disagreement) between them as well as a substantial number of cells each expert marked as low confidence (“difficult”) (Supplementary Figure 2B). In particular, trophozoites and gametocytes are prone to misclassification.

In light of this, in addition to comparing our predictions directly with expert annotations, we evaluated whether the results match the expected pattern for the time course images. Given the P. vivax life cycle, the number of parasites in the ring stage should decrease over time (until the parasites seed new cells and the cycle repeats), and the number in later stages should increase over time, consistent with expert counts and our results (Fig. 1d). We used diffusion pseudotime [19] to create an unsupervised ordering of all the cells in the data set based on the features learned by the model, to see if these features can capture the known progression of the various parasite stages; previously, this sort of modeling has been used to show that deep learning features are useful in capturing other chronological progressions such as cell cycle phase (Supplementary Figure S3). The ordering of the cells matches the expected cell progression, which suggests the learned features capture important and biologically meaningful underlying cell information.

Conclusions

In summary, we find that state-of-the-art object detection with Keras R-CNN can be accomplished with just ~ 20 lines of code and little computer vision expertise required. As our aim was to implement an already-proven architecture, we did not focus here on optimizing and assessing model accuracy; performance could also improve even further given more annotated examples and better hyperparameter optimization. We emphasize that annotated example cell images are required to train the system, but many biologists may prefer marking bounding boxes rather than learning how to choose, operate and tune classical segmentation algorithms. The models trained in this work are freely available although tailored to specific applications; the open-source framework makes training for other applications and datasets relatively straightforward. We have also recently added additional architectures from the literature, such as Feature Pyramid Network (FPN) [20] and Mask R-CNN [21].

Keras R-CNN’s popularity was unexpected for a pre-1.0 release. It presently has more than 650 stars and forks on GitHub, making it one of the most popular codebases available on the Broad Institute GitHub organization. Machine learning based computer vision algorithms have the potential to greatly improve the accuracy of image analysis for biology and decrease reliance on human labor, by reducing manual image analysis as well as time spent configuring automated algorithms. Keras R-CNN is therefore a useful tool for performing automated cell identification for both brightfield and fluorescence images, and can serve as a foundation for future point-and-click software.

Abbreviations

API

Application programming interface

BBBC

Broad Bioimage Benchmark Collection

DNA

Deoxyribonucleic acid

DSB

Data Science Bowl

FPN

Feature Pyramid Network

IoU

Intersection over union

P. vivax

Plasmodium vivax

R-CNN

Region-based convolutional neural network

Authors’ contributions

JH designed the project, collected malaria image data, co-wrote Keras R-CNN, developed methodology, and drafted the manuscript. AG co-wrote Keras R-CNN and ran experiments. DR prepared and provided Brazilian samples and consulted on methodology and interpretation of the data. SL prepared and provided Brazilian samples and annotated. GR prepared and provided time course malaria samples and annotated. OAN prepared time course malaria samples from Brazil. BM prepared Southeast Asian malaria samples. FN prepared Southeast Asian malaria samples. MUF and ML prepared Brazilian samples. LR organised malaria slide collections from Thailand and read and corrected the manuscript. MD consulted on methodology and supervised in vitro culture work. FTMC consulted on methodology and interpretation of the data and co-supervised the project. MM consulted on methodology and interpretation of the data and supervised the project. AEC designed and supervised the project and contributed to the manuscript.

Funding

Funding was provided by the National Institute of General Medical Sciences of the National Institutes of Health under R01 GM089652 and MIRA R35 GM122547 (to AEC). MM is supported by a career development award from BWF and a Wolfson Merit award from the Royal Society. DR was supported by a graduate fellowship (DGE1144152) from the U.S. National Science Foundation. FTMC is supported by FAPESP Grant 2017/18611–7. MVGL, MUF and FTMC are CNPq research fellows. GWR was supported by the HHMI Gilliam Fellowship for Advanced Study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Availability of data and materials

Availability and requirements:

Project name: Keras R-CNN.

Project home page: https://github.com/broadinstitute/keras-rcnn

Operating system: Platform independent.

Programming language: Python 3.

Other requirements: keras-resnet, numpy, tensorflow==1.13.1, Keras==2.2.4, scikit-image==0.15.0.

License: BSD.

The model weights can be found in keras_rcnn.applications. JHung2019.

The datasets supporting the conclusions of this article are available in the following:

Malaria data are available at https://data.broadinstitute.org/bbbc/BBBC041/.

Nuclei data are available at https://data.broadinstitute.org/bbbc/BBBC022/.

Ethics approval and consent to participate

Samples from Manaus, Brazil. All patients signed an informed consent form, and no children were included in the study. Sample collection was approved by Fundação de Medicina Tropical Ethical Board under the number CAAE 0044.0.114.000–11.

Samples from Acre, Brazil. Informed consent was obtained from all patients or, in case of children, from their parents/guardians. Study protocols for parasite sample collection were approved by the Institutional Review Board of the Institute of Biomedical Sciences, University of São Paulo, Brazil (1169/CEPSH, 2014).

Samples from Thailand. All patients signed an informed consent form, and no children were included in the study. The clinical samples were collected and tested in accordance with protocols approved by The Center for Clinical Vaccinology and Tropical Medicine at University of Oxford (OXTREC 17–11). Five mL of whole blood were collected in lithium heparin collection tubes. Samples were cryopreserved in Glycerolyte 57 (Baxter) after leukocyte depletion using cellulose columns (Sigma cat #C6288) (Sriprawat K, et al. Effective and cheap removal of leukocytes and platelets from Plasmodium vivax infected blood. Malar J 8, 115; 2009).

Consent for publication

Not Applicable.

Competing interests

The authors declare no competing interests.

Supplementary information

Supplementary information accompanies this paper at 10.1186/s12859-020-03635-x.