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Automatic localization and identification of mitochondria in cellular electron cryo-tomography using faster-RCNN.
Li, Ran; Zeng, Xiangrui; Sigmund, Stephanie E; Lin, Ruogu; Zhou, Bo; Liu, Chang; Wang, Kaiwen; Jiang, Rui; Freyberg, Zachary; Lv, Hairong; Xu, Min.
Affiliation
  • Li R; Department of Automation, Tsinghua University, Beijing, China.
  • Zeng X; Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA.
  • Sigmund SE; Department of Cellular, Molecular and Biophysical Studies, Columbia University Medical Center, New York, NY, USA.
  • Lin R; Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA.
  • Zhou B; Robotics Institute, Carnegie Mellon University, Pittsburgh, PA, USA.
  • Liu C; Department of Electrical and Computer Engineering, Carnegie Mellon University, Pittsburgh, PA, USA.
  • Wang K; Department of Electrical and Computer Engineering, Carnegie Mellon University, Pittsburgh, PA, USA.
  • Jiang R; Department of Automation, Tsinghua University, Beijing, China.
  • Freyberg Z; Departments of Psychiatry and Cell Biology, University of Pittsburgh, Pittsburgh, PA, USA. freybergzz@upmc.edu.
  • Lv H; Department of Automation, Tsinghua University, Beijing, China. lihua@ict.ac.cn.
  • Xu M; Computational Biology Department, Carnegie Mellon University, Pittsburgh, PA, USA. mxu1@cs.cmu.edu.
BMC Bioinformatics ; 20(Suppl 3): 132, 2019 Mar 29.
Article in En | MEDLINE | ID: mdl-30925860
BACKGROUND: Cryo-electron tomography (cryo-ET) enables the 3D visualization of cellular organization in near-native state which plays important roles in the field of structural cell biology. However, due to the low signal-to-noise ratio (SNR), large volume and high content complexity within cells, it remains difficult and time-consuming to localize and identify different components in cellular cryo-ET. To automatically localize and recognize in situ cellular structures of interest captured by cryo-ET, we proposed a simple yet effective automatic image analysis approach based on Faster-RCNN. RESULTS: Our experimental results were validated using in situ cyro-ET-imaged mitochondria data. Our experimental results show that our algorithm can accurately localize and identify important cellular structures on both the 2D tilt images and the reconstructed 2D slices of cryo-ET. When ran on the mitochondria cryo-ET dataset, our algorithm achieved Average Precision >0.95. Moreover, our study demonstrated that our customized pre-processing steps can further improve the robustness of our model performance. CONCLUSIONS: In this paper, we proposed an automatic Cryo-ET image analysis algorithm for localization and identification of different structure of interest in cells, which is the first Faster-RCNN based method for localizing an cellular organelle in Cryo-ET images and demonstrated the high accuracy and robustness of detection and classification tasks of intracellular mitochondria. Furthermore, our approach can be easily applied to detection tasks of other cellular structures as well.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neural Networks, Computer / Electron Microscope Tomography / Mitochondria Type of study: Diagnostic_studies Limits: Animals Language: En Journal: BMC Bioinformatics Journal subject: INFORMATICA MEDICA Year: 2019 Document type: Article Affiliation country: China Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neural Networks, Computer / Electron Microscope Tomography / Mitochondria Type of study: Diagnostic_studies Limits: Animals Language: En Journal: BMC Bioinformatics Journal subject: INFORMATICA MEDICA Year: 2019 Document type: Article Affiliation country: China Country of publication: United kingdom