Dataset Information

Detection of masses in mammograms using a one-stage object detector based on a deep convolutional neural network.

ABSTRACT: Several computer aided diagnosis (CAD) systems have been developed for mammography. They are widely used in certain countries such as the U.S. where mammography studies are conducted more frequently; however, they are not yet globally employed for clinical use due to their inconsistent performance, which can be attributed to their reliance on hand-crafted features. It is difficult to use hand-crafted features for mammogram images that vary due to factors such as the breast density of patients and differences in imaging devices. To address these problems, several studies have leveraged a deep convolutional neural network that does not require hand-crafted features. Among the recent object detectors, RetinaNet is particularly promising as it is a simpler one-stage object detector that is fast and efficient while achieving state-of-the-art performance. RetinaNet has been proven to perform conventional object detection tasks but has not been tested on detecting masses in mammograms. Thus, we propose a mass detection model based on RetinaNet. To validate its performance in diverse use cases, we construct several experimental setups using the public dataset INbreast and the in-house dataset GURO. In addition to training and testing on the same dataset (i.e., training and testing on INbreast), we evaluate our mass detection model in setups using additional training data (i.e., training on INbreast + GURO and testing on INbreast). We also evaluate our model in setups using pre-trained weights (i.e., using weights pre-trained on GURO, training and testing on INbreast). In all the experiments, our mass detection model achieves comparable or better performance than more complex state-of-the-art models including the two-stage object detector. Also, the results show that using the weights pre-trained on datasets achieves similar performance as directly using datasets in the training phase. Therefore, we make our mass detection model's weights pre-trained on both GURO and INbreast publicly available. We expect that researchers who train RetinaNet on their in-house dataset for the mass detection task can use our pre-trained weights to leverage the features extracted from the datasets.

SUBMITTER: Jung H

PROVIDER: S-EPMC6143189 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

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Detection of masses in mammograms using a one-stage object detector based on a deep convolutional neural network.

Jung Hwejin H Kim Bumsoo B Lee Inyeop I Yoo Minhwan M Lee Junhyun J Ham Sooyoun S Woo Okhee O Kang Jaewoo J

PloS one 20180918 9

Several computer aided diagnosis (CAD) systems have been developed for mammography. They are widely used in certain countries such as the U.S. where mammography studies are conducted more frequently; however, they are not yet globally employed for clinical use due to their inconsistent performance, which can be attributed to their reliance on hand-crafted features. It is difficult to use hand-crafted features for mammogram images that vary due to factors such as the breast density of patients an ...[more]

PMID: 30226841

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Project description:BackgroundThe detection of masses on mammogram represents one of the earliest signs of a malignant breast cancer. However, masses may be hard to detect due to dense breast tissue, leading to false negative results. In this study, we aimed to explore the clinical application of the convolutional neural network (CNN)-based deep learning (DL) system constructed in our previous work as an objective and accurate tool for breast cancer screening and diagnosis in Asian women.MethodsThis retrospective analysis included 324 patients with masses detected on mammograms at Shenzhen People's Hospital between April and December 2019. (I) Detection: images were independently analyzed by two junior radiologists who were blinded to relative results. Then, a senior radiologist analyzed the images after reviewing all the relevant information as the reference. (II) Classification: masses were classified by the same two junior radiologists and in consensus by two other seniors. Images were also input into the DL system. The sensitivity of detection by junior radiologists and the DL system, effects of different factors [breast density; patient age; morphology, margin, size, breast imaging reporting and data system (BI-RADS) category of the mass] on detection, the accuracy, sensitivity, and specificity of classification, and the area under the receiver operating characteristic (ROC) curve (AUC), were evaluated.ResultsA total of 618 masses were detected. The detection sensitivity of the two junior radiologists [78.0% (482/618) and 84.0% (519/618), respectively] was lower than that of the DL system [86.2% (533/618)]. Breast density significantly affected the detection by two junior radiologists (both P=0.030), but not by the DL system (P=0.385). The AUC for classifying masses as negative (BI-RADS 1, 2, 3) or positive (BI-RADS 4A, 4B, 4C, 5) for the DL system was significantly higher compared to those of the two junior radiologists, but not significantly different compared to seniors [DL system, 0.697; junior, 0.612 and 0.620 (P=0.021, 0.019); senior in consensus, 0.748 (P=0.071)].ConclusionsThe CNN-based DL system could assist junior radiologists in improving mass detection and is not affected by breast density. This DL system may have clinical utility in women with dense breasts, including reducing the impact caused by inexperienced radiologists and the potential for missed diagnoses.

Project description:Motivation:A majority of known genetic variants associated with human-inherited diseases lie in non-coding regions that lack adequate interpretation, making it indispensable to systematically discover functional sites at the whole genome level and precisely decipher their implications in a comprehensive manner. Although computational approaches have been complementing high-throughput biological experiments towards the annotation of the human genome, it still remains a big challenge to accurately annotate regulatory elements in the context of a specific cell type via automatic learning of the DNA sequence code from large-scale sequencing data. Indeed, the development of an accurate and interpretable model to learn the DNA sequence signature and further enable the identification of causative genetic variants has become essential in both genomic and genetic studies. Results:We proposed Deopen, a hybrid framework mainly based on a deep convolutional neural network, to automatically learn the regulatory code of DNA sequences and predict chromatin accessibility. In a series of comparison with existing methods, we show the superior performance of our model in not only the classification of accessible regions against background sequences sampled at random, but also the regression of DNase-seq signals. Besides, we further visualize the convolutional kernels and show the match of identified sequence signatures and known motifs. We finally demonstrate the sensitivity of our model in finding causative noncoding variants in the analysis of a breast cancer dataset. We expect to see wide applications of Deopen with either public or in-house chromatin accessibility data in the annotation of the human genome and the identification of non-coding variants associated with diseases. Availability and implementation:Deopen is freely available at https://github.com/kimmo1019/Deopen. Contact:ruijiang@tsinghua.edu.cn. Supplementary information:Supplementary data are available at Bioinformatics online.

Dataset Information

Detection of masses in mammograms using a one-stage object detector based on a deep convolutional neural network.

Publications

Detection of masses in mammograms using a one-stage object detector based on a deep convolutional neural network.

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