Evidence map›Paper›PMID 31511756›Full record

ArticleMachine vision and applications2018

Improved deep learning-based macromolecules structure classification from electron cryo-tomograms.

Chengqian Che, Ruogu Lin, Xiangrui Zeng, Karim Elmaaroufi, John Galeotti, Min Xu

Abstract read
In one paragraph

Article in Machine vision and applications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

  1. Article
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  7. Review
  8. Review
  9. High-throughput cryo-ET structural pattern mining by unsupervised deep iterative subtomogram clustering.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Computational methods forFrontiers in cellular and infection microbiology · 2023
    Review
  11. Review
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Chengqian CheThe Robotics Institute, Carnegie Mellon University,Pittsburgh, USA.
Ruogu LinDepartment of Automation, Tsinghua University, Beijing, China.
Xiangrui ZengComputational Biology Department, Carnegie Mellon University, Pittsburgh, USA.
Karim ElmaaroufiDepartment of Electrical and Computer Engineering, Carnegie Mellon University, Pittsburgh, USA.
John GaleottiThe Robotics Institute, Carnegie Mellon University,Pittsburgh, USA.
Min XuComputational Biology Department, Carnegie Mellon University, Pittsburgh, USA.ORCID 0000-0002-0881-5891

Funding

TrainingP41GM103712 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FAEDER, JAMES · 2012 to 2021
$16.3M
Microsurgical In-Situ Image Guidance with Optical Coherence TomographyR01EY021641 · NEI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLATZKY, ROBERTA L, STETTEN, GEORGE D. · 2011 to 2014
$2.2M
NEI NIH HHS R01 EY021641NIGMS NIH HHS P41 GM103712
6 · The paper itself

Abstract

Cellular processes are governed by macromolecular complexes inside the cell. Study of the native structures of macromolecular complexes has been extremely difficult due to lack of data. With recent breakthroughs in Cellular Electron Cryo-Tomography (CECT) 3D imaging technology, it is now possible for researchers to gain accesses to fully study and understand the macro-molecular structures single cells. However, systematic recovery of macromolecular structures from CECT is very difficult due to high degree of structural complexity and practical imaging limitations. Specifically, we proposed a deep learning-based image classification approach for large-scale systematic macromolecular structure separation from CECT data. However, our previous work was only a very initial step toward exploration of the full potential of deep learning-based macromolecule separation. In this paper, we focus on improving classification performance by proposing three newly designed individual CNN models: an extended version of (Deep Small Receptive Field) DSRF3D, donated as DSRF3D-v2, a 3D residual block-based neural network, named as RB3D, and a convolutional 3D (C3D)-based model, CB3D. We compare them with our previously developed model (DSRF3D) on 12 datasets with different SNRs and tilt angle ranges. The experiments show that our new models achieved significantly higher classification accuracies. The accuracies are not only higher than 0.9 on normal datasets, but also demonstrate potentials to operate on datasets with high levels of noises and missing wedge effects presented.

Indexed as

Cellular electron cryo-tomographyDeep learningImage classificationMedical big data learning

Identifiers

PMID31511756
PMCPMC6738941

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.