COLI‐Net: Deep learning‐assisted fully automated COVID‐19 lung and infection pneumonia lesion detection and segmentation from chest computed tomography images. Issue 1 (28th October 2021)
- Record Type:
- Journal Article
- Title:
- COLI‐Net: Deep learning‐assisted fully automated COVID‐19 lung and infection pneumonia lesion detection and segmentation from chest computed tomography images. Issue 1 (28th October 2021)
- Main Title:
- COLI‐Net: Deep learning‐assisted fully automated COVID‐19 lung and infection pneumonia lesion detection and segmentation from chest computed tomography images
- Authors:
- Shiri, Isaac
Arabi, Hossein
Salimi, Yazdan
Sanaat, Amirhossein
Akhavanallaf, Azadeh
Hajianfar, Ghasem
Askari, Dariush
Moradi, Shakiba
Mansouri, Zahra
Pakbin, Masoumeh
Sandoughdaran, Saleh
Abdollahi, Hamid
Radmard, Amir Reza
Rezaei‐Kalantari, Kiara
Ghelich Oghli, Mostafa
Zaidi, Habib - Abstract:
- Abstract: We present a deep learning (DL)‐based automated whole lung and COVID‐19 pneumonia infectious lesions (COLI‐Net) detection and segmentation from chest computed tomography (CT) images. This multicenter/multiscanner study involved 2368 (347′259 2D slices) and 190 (17 341 2D slices) volumetric CT exams along with their corresponding manual segmentation of lungs and lesions, respectively. All images were cropped, resized, and the intensity values clipped and normalized. A residual network with non‐square Dice loss function built upon TensorFlow was employed. The accuracy of lung and COVID‐19 lesions segmentation was evaluated on an external reverse transcription‐polymerase chain reaction positive COVID‐19 dataset (7′333 2D slices) collected at five different centers. To evaluate the segmentation performance, we calculated different quantitative metrics, including radiomic features. The mean Dice coefficients were 0.98 ± 0.011 (95% CI, 0.98–0.99) and 0.91 ± 0.038 (95% CI, 0.90–0.91) for lung and lesions segmentation, respectively. The mean relative Hounsfield unit differences were 0.03 ± 0.84% (95% CI, −0.12 to 0.18) and −0.18 ± 3.4% (95% CI, −0.8 to 0.44) for the lung and lesions, respectively. The relative volume difference for lung and lesions were 0.38 ± 1.2% (95% CI, 0.16–0.59) and 0.81 ± 6.6% (95% CI, −0.39 to 2), respectively. Most radiomic features had a mean relative error less than 5% with the highest mean relative error achieved for the lung for the rangeAbstract: We present a deep learning (DL)‐based automated whole lung and COVID‐19 pneumonia infectious lesions (COLI‐Net) detection and segmentation from chest computed tomography (CT) images. This multicenter/multiscanner study involved 2368 (347′259 2D slices) and 190 (17 341 2D slices) volumetric CT exams along with their corresponding manual segmentation of lungs and lesions, respectively. All images were cropped, resized, and the intensity values clipped and normalized. A residual network with non‐square Dice loss function built upon TensorFlow was employed. The accuracy of lung and COVID‐19 lesions segmentation was evaluated on an external reverse transcription‐polymerase chain reaction positive COVID‐19 dataset (7′333 2D slices) collected at five different centers. To evaluate the segmentation performance, we calculated different quantitative metrics, including radiomic features. The mean Dice coefficients were 0.98 ± 0.011 (95% CI, 0.98–0.99) and 0.91 ± 0.038 (95% CI, 0.90–0.91) for lung and lesions segmentation, respectively. The mean relative Hounsfield unit differences were 0.03 ± 0.84% (95% CI, −0.12 to 0.18) and −0.18 ± 3.4% (95% CI, −0.8 to 0.44) for the lung and lesions, respectively. The relative volume difference for lung and lesions were 0.38 ± 1.2% (95% CI, 0.16–0.59) and 0.81 ± 6.6% (95% CI, −0.39 to 2), respectively. Most radiomic features had a mean relative error less than 5% with the highest mean relative error achieved for the lung for the range first‐order feature (−6.95%) and least axis length shape feature (8.68%) for lesions. We developed an automated DL‐guided three‐dimensional whole lung and infected regions segmentation in COVID‐19 patients to provide fast, consistent, robust, and human error immune framework for lung and pneumonia lesion detection and quantification. … (more)
- Is Part Of:
- International journal of imaging systems and technology. Volume 32:Issue 1(2022)
- Journal:
- International journal of imaging systems and technology
- Issue:
- Volume 32:Issue 1(2022)
- Issue Display:
- Volume 32, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 32
- Issue:
- 1
- Issue Sort Value:
- 2022-0032-0001-0000
- Page Start:
- 12
- Page End:
- 25
- Publication Date:
- 2021-10-28
- Subjects:
- COVID‐19 -- deep learning -- pneumonia -- segmentation -- X‐ray CT
Imaging systems -- Periodicals
Image processing -- Periodicals
621.367 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1098 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ima.22672 ↗
- Languages:
- English
- ISSNs:
- 0899-9457
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.299000
British Library DSC - BLDSS-3PM
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- 26270.xml