Abstract:Accurate classification of blood cells is of vital significance in the diagnosis of hematological disorders. However, in real-world scenarios, domain shifts caused by the variability in laboratory procedures and settings, result in a rapid deterioration of the model's generalization performance. To address this issue, we propose a novel framework of domain-invariant representation learning (DoRL) via segment anything model (SAM) for blood cell classification. The DoRL comprises two main components: a LoRA-based SAM (LoRA-SAM) and a cross-domain autoencoder (CAE). The advantage of DoRL is that it can extract domain-invariant representations from various blood cell datasets in an unsupervised manner. Specifically, we first leverage the large-scale foundation model of SAM, fine-tuned with LoRA, to learn general image embeddings and segment blood cells. Additionally, we introduce CAE to learn domain-invariant representations across different-domain datasets while mitigating images' artifacts. To validate the effectiveness of domain-invariant representations, we employ five widely used machine learning classifiers to construct blood cell classification models. Experimental results on two public blood cell datasets and a private real dataset demonstrate that our proposed DoRL achieves a new state-of-the-art cross-domain performance, surpassing existing methods by a significant margin. The source code can be available at the URL (https://github.com/AnoK3111/DoRL).
Abstract:Accurate classification of blood cells plays a vital role in hematological analysis as it aids physicians in diagnosing various medical conditions. In this study, we present a novel approach for classifying blood cell images known as BC-SAM. BC-SAM leverages the large-scale foundation model of Segment Anything Model (SAM) and incorporates a fine-tuning technique using LoRA, allowing it to extract general image embeddings from blood cell images. To enhance the applicability of BC-SAM across different blood cell image datasets, we introduce an unsupervised cross-domain autoencoder that focuses on learning intrinsic features while suppressing artifacts in the images. To assess the performance of BC-SAM, we employ four widely used machine learning classifiers (Random Forest, Support Vector Machine, Artificial Neural Network, and XGBoost) to construct blood cell classification models and compare them against existing state-of-the-art methods. Experimental results conducted on two publicly available blood cell datasets (Matek-19 and Acevedo-20) demonstrate that our proposed BC-SAM achieves a new state-of-the-art result, surpassing the baseline methods with a significant improvement. The source code of this paper is available at https://github.com/AnoK3111/BC-SAM.
Abstract:Effective and accurate diagnosis of Diabetes Mellitus (DM), as well as its early stage Impaired Glucose Regulation (IGR), has attracted much attention recently. Traditional Chinese Medicine (TCM) [3], [5] etc. has proved that tongue, face and sublingual diagnosis as a noninvasive method is a reasonable way for disease detection. However, most previous works only focus on a single modality (tongue, face or sublingual) for diagnosis, although different modalities may provide complementary information for the diagnosis of DM and IGR. In this paper, we propose a novel multi-modal classification method to discriminate between DM (or IGR) and healthy controls. Specially, the tongue, facial and sublingual images are first collected by using a non-invasive capture device. The color, texture and geometry features of these three types of images are then extracted, respectively. Finally, our so-called multi-modal similar and specific learning (MMSSL) approach is proposed to combine features of tongue, face and sublingual, which not only exploits the correlation but also extracts individual components among them. Experimental results on a dataset consisting of 192 Healthy, 198 DM and 114 IGR samples (all samples were obtained from Guangdong Provincial Hospital of Traditional Chinese Medicine) substantiate the effectiveness and superiority of our proposed method for the diagnosis of DM and IGR, compared to the case of using a single modality.