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Juan C. Caicedo

Publications and source records attributed to Juan C. Caicedo.

12 recordsLinked to original sources

CHAMMI-75: Pre-training multi-channel models with heterogeneous microscopy images

Quantifying cell morphology using images and machine learning has proven to be a powerful tool to study the response of cells to treatments. However, models used to quantify cellular morphology are typically trained with a single microscopy imaging type. This results in specialized models that cannot be reused across biological studies because the technical specifications do not match (e.g., different number of channels). Here, we present CHAMMI-75, an open access dataset of heterogeneous, multi-channel microscopy images from 75 diverse biological studies. We curated this resource from publicly available sources to investigate cellular morphology models that are channel-adaptive and can process any microscopy image type. Our experiments show that training with CHAMMI-75 can improve performance in multi-channel bioimaging tasks primarily because of its high diversity in microscopy modalities. This work paves the way to create the next generation of cellular morphology models for biological studies.

cs.CV↗

Progress and new challenges in image-based profiling

For over two decades, image-based profiling has revolutionized cell phenotype analysis. Image-based profiling processes rich, high-throughput, microscopy data into thousands of unbiased measurements that reveal phenotypic patterns powerful for drug discovery, functional genomics, and cell state classification. Here, we review the evolving computational landscape of image-based profiling, detailing the bioinformatics processes involved from feature extraction to normalization and batch correction. We discuss how deep learning has fundamentally reshaped the field. We examine key methodological advancements, such as single-cell analysis, the development of robust similarity metrics, and the expansion into new modalities like optical pooled screening, temporal imaging, and 3D organoid profiling. We also highlight the growth of public benchmarks and open-source software ecosystems as a key driver for fostering reproducibility and collaboration. Despite these advances, the field still faces substantial challenges, particularly in developing methods for emerging temporal and 3D data modalities, establishing robust quality control standards and workflows, and interpreting the processed features. By focusing on the technical evolution of image-based profiling rather than the wide-ranging biological applications, our aim with this review is to provide researchers with a roadmap for navigating the progress and new challenges in this rapidly advancing domain.

q-bio.QM↗

ChA-MAEViT: Unifying Channel-Aware Masked Autoencoders and Multi-Channel Vision Transformers for Improved Cross-Channel Learning

Prior work using Masked Autoencoders (MAEs) typically relies on random patch masking based on the assumption that images have significant redundancies across different channels, allowing for the reconstruction of masked content using cross-channel correlations. However, this assumption does not hold in Multi-Channel Imaging (MCI), where channels may provide complementary information with minimal feature overlap. Thus, these MAEs primarily learn local structures within individual channels from patch reconstruction, failing to fully leverage cross-channel interactions and limiting their MCI effectiveness. In this paper, we present ChA-MAEViT, an MAE-based method that enhances feature learning across MCI channels via four key strategies: (1) dynamic channel-patch masking, which compels the model to reconstruct missing channels in addition to masked patches, thereby enhancing cross-channel dependencies and improving robustness to varying channel configurations; (2) memory tokens, which serve as long-term memory aids to promote information sharing across channels, addressing the challenges of reconstructing structurally diverse channels; (3) hybrid token fusion module, which merges fine-grained patch tokens with a global class token to capture richer representations; and (4) Channel-Aware Decoder, a lightweight decoder utilizes channel tokens to effectively reconstruct image patches. Experiments on satellite and microscopy datasets, CHAMMI, JUMP-CP, and So2Sat, show that ChA-MAEViT significantly outperforms state-of-the-art MCI-ViTs by 3.0-21.5%, highlighting the importance of cross-channel interactions in MCI. Our code is publicly available at https://github.com/chaudatascience/cha_mae_vit.

cs.CV↗

Synthesizing Late-Stage Contrast Enhancement in Breast MRI: A Comprehensive Pipeline Leveraging Temporal Contrast Enhancement Dynamics

Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) is essential for breast cancer diagnosis due to its ability to characterize tissue through contrast agent kinetics. However, traditional DCE-MRI protocols require multiple imaging phases, including early and late post-contrast acquisitions, leading to prolonged scan times, patient discomfort, motion artifacts, high costs, and limited accessibility. To overcome these limitations, this study presents a pipeline for synthesizing late-phase DCE-MRI images from early-phase data, replicating the time-intensity (TI) curve behavior in enhanced regions while maintaining visual fidelity across the entire image. The proposed approach introduces a novel loss function, Time Intensity Loss (TI-loss), leveraging the temporal behavior of contrast agents to guide the training of a generative model. Additionally, a new normalization strategy, TI-norm, preserves the contrast enhancement pattern across multiple image sequences at various timestamps, addressing limitations of conventional normalization methods. Two metrics are proposed to evaluate image quality: the Contrast Agent Pattern Score ($\mathcal{CP}_{s}$), which validates enhancement patterns in annotated regions, and the Average Difference in Enhancement ($\mathcal{ED}$), measuring differences between real and generated enhancements. Using a public DCE-MRI dataset with 1.5T and 3T scanners, the proposed method demonstrates accurate synthesis of late-phase images that outperform existing models in replicating the TI curve's behavior in regions of interest while preserving overall image quality. This advancement shows a potential to optimize DCE-MRI protocols by reducing scanning time without compromising diagnostic accuracy, and bringing generative models closer to practical implementation in clinical scenarios to enhance efficiency in breast cancer imaging.

cs.CV↗

Reproducible image-based profiling with Pycytominer

Advances in high-throughput microscopy have enabled the rapid acquisition of large numbers of high-content microscopy images. Whether by deep learning or classical algorithms, image analysis pipelines then produce single-cell features. To process these single-cells for downstream applications, we present Pycytominer, a user-friendly, open-source python package that implements the bioinformatics steps, known as image-based profiling. We demonstrate Pycytominers usefulness in a machine learning project to predict nuisance compounds that cause undesirable cell injuries.

q-bio.QM↗

CHAMMI: A benchmark for channel-adaptive models in microscopy imaging

Most neural networks assume that input images have a fixed number of channels (three for RGB images). However, there are many settings where the number of channels may vary, such as microscopy images where the number of channels changes depending on instruments and experimental goals. Yet, there has not been a systemic attempt to create and evaluate neural networks that are invariant to the number and type of channels. As a result, trained models remain specific to individual studies and are hardly reusable for other microscopy settings. In this paper, we present a benchmark for investigating channel-adaptive models in microscopy imaging, which consists of 1) a dataset of varied-channel single-cell images, and 2) a biologically relevant evaluation framework. In addition, we adapted several existing techniques to create channel-adaptive models and compared their performance on this benchmark to fixed-channel, baseline models. We find that channel-adaptive models can generalize better to out-of-domain tasks and can be computationally efficient. We contribute a curated dataset (https://doi.org/10.5281/zenodo.7988357) and an evaluation API (https://github.com/broadinstitute/MorphEm.git) to facilitate objective comparisons in future research and applications.

cs.CV↗

Out of Distribution Generalization via Interventional Style Transfer in Single-Cell Microscopy

Real-world deployment of computer vision systems, including in the discovery processes of biomedical research, requires causal representations that are invariant to contextual nuisances and generalize to new data. Leveraging the internal replicate structure of two novel single-cell fluorescent microscopy datasets, we propose generally applicable tests to assess the extent to which models learn causal representations across increasingly challenging levels of OOD-generalization. We show that despite seemingly strong performance, as assessed by other established metrics, both naive and contemporary baselines designed to ward against confounding, collapse on these tests. We introduce a new method, Interventional Style Transfer (IST), that substantially improves OOD generalization by generating interventional training distributions in which spurious correlations between biological causes and nuisances are mitigated. We publish our code and datasets.

cs.CV↗

Roadmap on Deep Learning for Microscopy

Through digital imaging, microscopy has evolved from primarily being a means for visual observation of life at the micro- and nano-scale, to a quantitative tool with ever-increasing resolution and throughput. Artificial intelligence, deep neural networks, and machine learning are all niche terms describing computational methods that have gained a pivotal role in microscopy-based research over the past decade. This Roadmap is written collectively by prominent researchers and encompasses selected aspects of how machine learning is applied to microscopy image data, with the aim of gaining scientific knowledge by improved image quality, automated detection, segmentation, classification and tracking of objects, and efficient merging of information from multiple imaging modalities. We aim to give the reader an overview of the key developments and an understanding of possibilities and limitations of machine learning for microscopy. It will be of interest to a wide cross-disciplinary audience in the physical sciences and life sciences.

physics.optics↗

Anchoring to Exemplars for Training Mixture-of-Expert Cell Embeddings

Analyzing the morphology of cells in microscopy images can provide insights into the mechanism of compounds or the function of genes. Addressing this task requires methods that can not only extract biological information from the images, but also ignore technical variations, ie, changes in experimental procedure or differences between equipments used to collect microscopy images. We propose Treatment ExemplArs with Mixture-of-experts (TEAMs), an embedding learning approach that learns a set of experts that are specialized in capturing technical variations in our training set and then aggregates specialist's predictions at test time. Thus, TEAMs can learn powerful embeddings with less technical variation bias by minimizing the noise from every expert. To train our model, we leverage Treatment Exemplars that enable our approach to capture the distribution of the entire dataset in every minibatch while still fitting into GPU memory. We evaluate our approach on three datasets for tasks like drug discovery, boosting performance on identifying the true mechanism of action of cell treatments by 5.5-11% over the state-of-the-art.

cs.LG↗

Quantum Latent Semantic Analysis

The main goal of this paper is to explore latent topic analysis (LTA), in the context of quantum information retrieval. LTA is a valuable technique for document analysis and representation, which has been extensively used in information retrieval and machine learning. Different LTA techniques have been proposed, some based on geometrical modeling (such as latent semantic analysis, LSA) and others based on a strong statistical foundation. However, these two different approaches are not usually mixed. Quantum information retrieval has the remarkable virtue of combining both geometry and probability in a common principled framework. We built on this quantum framework to propose a new LTA method, which has a clear geometrical motivation but also supports a well-founded probabilistic interpretation. An initial exploratory experimentation was performed on three standard data sets. The results show that the proposed method outperforms LSA on two of the three datasets. These results suggests that the quantum-motivated representation is an alternative for geometrical latent topic modeling worthy of further exploration.

cs.LG↗

Flickr30k Entities: Collecting Region-to-Phrase Correspondences for Richer Image-to-Sentence Models

The Flickr30k dataset has become a standard benchmark for sentence-based image description. This paper presents Flickr30k Entities, which augments the 158k captions from Flickr30k with 244k coreference chains, linking mentions of the same entities across different captions for the same image, and associating them with 276k manually annotated bounding boxes. Such annotations are essential for continued progress in automatic image description and grounded language understanding. They enable us to define a new benchmark for localization of textual entity mentions in an image. We present a strong baseline for this task that combines an image-text embedding, detectors for common objects, a color classifier, and a bias towards selecting larger objects. While our baseline rivals in accuracy more complex state-of-the-art models, we show that its gains cannot be easily parlayed into improvements on such tasks as image-sentence retrieval, thus underlining the limitations of current methods and the need for further research.

cs.CV↗

Active Object Localization with Deep Reinforcement Learning

We present an active detection model for localizing objects in scenes. The model is class-specific and allows an agent to focus attention on candidate regions for identifying the correct location of a target object. This agent learns to deform a bounding box using simple transformation actions, with the goal of determining the most specific location of target objects following top-down reasoning. The proposed localization agent is trained using deep reinforcement learning, and evaluated on the Pascal VOC 2007 dataset. We show that agents guided by the proposed model are able to localize a single instance of an object after analyzing only between 11 and 25 regions in an image, and obtain the best detection results among systems that do not use object proposals for object localization.

cs.CV↗