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1.
Heliyon ; 10(7): e29050, 2024 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-38623206

RESUMO

Background: Anesthesiology plays a crucial role in perioperative care, critical care, and pain management, impacting patient experiences and clinical outcomes. However, our understanding of the anesthesiology research landscape is limited. Accordingly, we initiated a data-driven analysis through topic modeling to uncover research trends, enabling informed decision-making and fostering progress within the field. Methods: The easyPubMed R package was used to collect 32,300 PubMed abstracts spanning from 2000 to 2022. These abstracts were authored by 737 Anesthesiology Principal Investigators (PIs) who were recipients of National Institute of Health (NIH) funding from 2010 to 2022. Abstracts were preprocessed, vectorized, and analyzed with the state-of-the-art BERTopic algorithm to identify pillar topics and trending subtopics within anesthesiology research. Temporal trends were assessed using the Mann-Kendall test. Results: The publishing journals with most abstracts in this dataset were Anesthesia & Analgesia 1133, Anesthesiology 992, and Pain 671. Eight pillar topics were identified and categorized as basic or clinical sciences based on a hierarchical clustering analysis. Amongst the pillar topics, "Cells & Proteomics" had both the highest annual and total number of abstracts. Interestingly, there was an overall upward trend for all topics spanning the years 2000-2022. However, when focusing on the period from 2015 to 2022, topics "Cells & Proteomics" and "Pulmonology" exhibit a downward trajectory. Additionally, various subtopics were identified, with notable increasing trends in "Aneurysms", "Covid 19 Pandemic", and "Artificial intelligence & Machine Learning". Conclusion: Our work offers a comprehensive analysis of the anesthesiology research landscape by providing insights into pillar topics, and trending subtopics. These findings contribute to a better understanding of anesthesiology research and can guide future directions.

2.
Am J Obstet Gynecol ; 230(1S): S46, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-38355237

RESUMO

This article has been retracted: please see Elsevier Policy on Article Withdrawal (https://www.elsevier.com/about/policies/article-withdrawal). This meeting abstract has been retracted at the request of the authors. The team determined further analysis is warranted before the formal presentation of the results.

3.
Comput Methods Programs Biomed ; 224: 107019, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-35878483

RESUMO

BACKGROUND AND OBJECTIVE: Leukemia represents 30% of all pediatric cancers and is considered the most common malignancy affecting adults and children. Cell differential count obtained from bone marrow aspirate smears is crucial for diagnosing hematologic diseases. Classification of these cell types is an essential task towards analyzing the disease, but it is time-consuming and requires intensive manual intervention. While machine learning has shown excellent outcomes in automating medical diagnosis, it needs ample data to build an efficient model for real-world tasks. This paper aims to generate synthetic data to enhance the classification accuracy of cells obtained from bone marrow aspirate smears. METHODS: A three-stage architecture has been proposed. We first collaborate with experts from the medical domain to prepare a dataset that consolidates microscopic cell images obtained from bone marrow aspirate smears from three different sources. The second stage involves a generative adversarial networks (GAN) model to generate synthetic microscopic cell images. We propose a GAN model consisting of three networks; generator discriminator and classifier. We train the GAN model with the loss function of Wasserstein GAN with gradient penalty (WGAN-GP). Since our GAN has an additional classifier and was trained using WGAN-GP, we named our model C-WGAN-GP. In the third stage, we propose a sequential convolutional neural network (CNN) to classify cells in the original and synthetic dataset to demonstrate how generating synthetic data and utilizing a simple sequential CNN model can enhance the accuracy of cell classification. RESULTS: We validated the proposed C-WGAN-GP and sequential CNN model with various evaluation metrics and achieved a classification accuracy of 96.98% using the synthetic dataset. We have presented each cell type's accuracy, specificity, and sensitivity results. The sequential CNN model achieves the highest accuracy for neutrophils with an accuracy rate of 97.5%. The highest value for sensitivity and specificity are 97.1% and 97%. Our proposed GAN model achieved an inception score of 14.52 ± 0.10, significantly better than the existing GAN models. CONCLUSIONS: Using three network GAN architecture produced more realistic synthetic data than existing models. Sequential CNN model with the synthetic data achieved higher classification accuracy than the original data.


Assuntos
Medula Óssea , Redes Neurais de Computação , Medula Óssea/diagnóstico por imagem , Criança , Humanos , Processamento de Imagem Assistida por Computador/métodos , Aprendizado de Máquina , Sensibilidade e Especificidade
4.
Int J Mol Sci ; 23(7)2022 Mar 28.
Artigo em Inglês | MEDLINE | ID: mdl-35409058

RESUMO

Nucleic acids are the basic units of deoxyribonucleic acid (DNA) sequencing. Every organism demonstrates different DNA sequences with specific nucleotides. It reveals the genetic information carried by a particular DNA segment. Nucleic acid sequencing expresses the evolutionary changes among organisms and revolutionizes disease diagnosis in animals. This paper proposes a generative adversarial networks (GAN) model to create synthetic nucleic acid sequences of the cat genome tuned to exhibit specific desired properties. We obtained the raw sequence data from Illumina next generation sequencing. Various data preprocessing steps were performed using Cutadapt and DADA2 tools. The processed data were fed to the GAN model that was designed following the architecture of Wasserstein GAN with gradient penalty (WGAN-GP). We introduced a predictor and an evaluator in our proposed GAN model to tune the synthetic sequences to acquire certain realistic properties. The predictor was built for extracting samples with a promoter sequence, and the evaluator was built for filtering samples that scored high for motif-matching. The filtered samples were then passed to the discriminator. We evaluated our model based on multiple metrics and demonstrated outputs for latent interpolation, latent complementation, and motif-matching. Evaluation results showed our proposed GAN model achieved 93.7% correlation with the original data and produced significant outcomes as compared to existing models for sequence generation.


Assuntos
Adenosina Desaminase , Processamento de Imagem Assistida por Computador , DNA , Processamento de Imagem Assistida por Computador/métodos , Peptídeos e Proteínas de Sinalização Intercelular
5.
Biology (Basel) ; 11(2)2022 Feb 10.
Artigo em Inglês | MEDLINE | ID: mdl-35205142

RESUMO

Every year approximately 1.24 million people are diagnosed with blood cancer. While the rate increases each year, the availability of data for each kind of blood cancer remains scarce. It is essential to produce enough data for each blood cell type obtained from bone marrow aspirate smears to diagnose rare types of cancer. Generating data would help easy and quick diagnosis, which are the most critical factors in cancer. Generative adversarial networks (GAN) are the latest emerging framework for generating synthetic images and time-series data. This paper takes microscopic cell images, preprocesses them, and uses a hybrid GAN architecture to generate synthetic images of the cell types containing fewer data. We prepared a single dataset with expert intervention by combining images from three different sources. The final dataset consists of 12 cell types and has 33,177 microscopic cell images. We use the discriminator architecture of auxiliary classifier GAN (AC-GAN) and combine it with the Wasserstein GAN with gradient penalty model (WGAN-GP). We name our model as WGAN-GP-AC. The discriminator in our proposed model works to identify real and generated images and classify every image with a cell type. We provide experimental results demonstrating that our proposed model performs better than existing individual and hybrid GAN models in generating microscopic cell images. We use the generated synthetic data with classification models, and the results prove that the classification rate increases significantly. Classification models achieved 0.95 precision and 0.96 recall value for synthetic data, which is higher than the original, augmented, or combined datasets.

6.
Biology (Basel) ; 9(12)2020 Dec 03.
Artigo em Inglês | MEDLINE | ID: mdl-33287366

RESUMO

Automating medical diagnosis and training medical students with real-life situations requires the accumulation of large dataset variants covering all aspects of a patient's condition. For preventing the misuse of patient's private information, datasets are not always publicly available. There is a need to generate synthetic data that can be trained for the advancement of public healthcare without intruding on patient's confidentiality. Currently, rules for generating synthetic data are predefined and they require expert intervention, which limits the types and amount of synthetic data. In this paper, we propose a novel generative adversarial networks (GAN) model, named SynSigGAN, for automating the generation of any kind of synthetic biomedical signals. We have used bidirectional grid long short-term memory for the generator network and convolutional neural network for the discriminator network of the GAN model. Our model can be applied in order to create new biomedical synthetic signals while using a small size of the original signal dataset. We have experimented with our model for generating synthetic signals for four kinds of biomedical signals (electrocardiogram (ECG), electroencephalogram (EEG), electromyography (EMG), photoplethysmography (PPG)). The performance of our model is superior wheen compared to other traditional models and GAN models, as depicted by the evaluation metric. Synthetic biomedical signals generated by our approach have been tested while using other models that could classify each signal significantly with high accuracy.

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