| dc.contributor |
Electrical and Computer Engineering |
|
| dc.creator |
Song, Yang |
|
| dc.creator |
Cai, Weidong |
|
| dc.creator |
Huang, Heng |
|
| dc.creator |
Wang, Yue |
|
| dc.creator |
Feng, David D. |
|
| dc.creator |
Chen, Mei |
|
| dc.date |
2013-07-10T10:37:45Z |
|
| dc.date |
2013-07-10T10:37:45Z |
|
| dc.date |
2013-06-02 |
|
| dc.date |
2013-07-10T10:37:45Z |
|
| dc.date.accessioned |
2023-03-01T18:54:00Z |
|
| dc.date.available |
2023-03-01T18:54:00Z |
|
| dc.identifier |
BMC Bioinformatics. 2013 Jun 02;14(1):173 |
|
| dc.identifier |
http://hdl.handle.net/10919/23296 |
|
| dc.identifier |
https://doi.org/10.1186/1471-2105-14-173 |
|
| dc.identifier.uri |
http://localhost:8080/xmlui/handle/CUHPOERS/281784 |
|
| dc.description |
Background
Segmenting cell nuclei in microscopic images has become one of the most important routines in modern biological applications. With the vast amount of data, automatic localization, i.e. detection and segmentation, of cell nuclei is highly desirable compared to time-consuming manual processes. However, automated segmentation is challenging due to large intensity inhomogeneities in the cell nuclei and the background.
Results
We present a new method for automated progressive localization of cell nuclei using data-adaptive models that can better handle the inhomogeneity problem. We perform localization in a three-stage approach: first identify all interest regions with contrast-enhanced salient region detection, then process the clusters to identify true cell nuclei with probability estimation via feature-distance profiles of reference regions, and finally refine the contours of detected regions with regional contrast-based graphical model. The proposed region-based progressive localization (RPL) method is evaluated on three different datasets, with the first two containing grayscale images, and the third one comprising of color images with cytoplasm in addition to cell nuclei. We demonstrate performance improvement over the state-of-the-art. For example, compared to the second best approach, on the first dataset, our method achieves 2.8 and 3.7 reduction in Hausdorff distance and false negatives; on the second dataset that has larger intensity inhomogeneity, our method achieves 5% increase in Dice coefficient and Rand index; on the third dataset, our method achieves 4% increase in object-level accuracy.
Conclusions
To tackle the intensity inhomogeneities in cell nuclei and background, a region-based progressive localization method is proposed for cell nuclei localization in fluorescence microscopy images. The RPL method is demonstrated highly effective on three different public datasets, with on average 3.5% and 7% improvement of region- and contour-based segmentation performance over the state-of-the-art. |
|
| dc.description |
Published version |
|
| dc.format |
application/pdf |
|
| dc.format |
text/xml |
|
| dc.format |
application/pdf |
|
| dc.language |
en_US |
|
| dc.rights |
Creative Commons Attribution 4.0 International |
|
| dc.rights |
http://creativecommons.org/licenses/by/4.0/ |
|
| dc.rights |
Yang Song et al.; licensee BioMed Central Ltd. |
|
| dc.title |
Region-based progressive localization of cell nuclei in microscopic images with data adaptive modeling |
|
| dc.title |
BMC Bioinformatics |
|
| dc.type |
Article - Refereed |
|
| dc.type |
Text |
|