Evidence map›Paper›PMID 36048824›Full record

ArticlePloS one2022

An intensity-based post-processing tool for 3D instance segmentation of organelles in soft X-ray tomograms.

Angdi Li, Shuning Zhang, Valentina Loconte, Yan Liu, Axel Ekman, Garth J Thompson, Andrej Sali, Raymond C Stevens, Kate White, Jitin Singla and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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

11 authors at 5 institutions in 3 countries.

Angdi LiiHuman Institute, ShanghaiTech University, Shanghai, China.ORCID 0000-0001-6143-6295
Shuning ZhangiHuman Institute, ShanghaiTech University, Shanghai, China.
Valentina LoconteiHuman Institute, ShanghaiTech University, Shanghai, China.
Yan LiuiHuman Institute, ShanghaiTech University, Shanghai, China.
Axel EkmanDepartment of Anatomy, University of California San Francisco, San Francisco, CA, United States of America.
Garth J ThompsoniHuman Institute, ShanghaiTech University, Shanghai, China.ORCID 0000-0002-1125-0799
Andrej SaliCalifornia Institute for Quantitative Biosciences, Department of Bioengineering and Therapeutic Sciences, Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, United States of America.
Raymond C StevensiHuman Institute, ShanghaiTech University, Shanghai, China.
Kate WhiteDepartment of Chemistry, Bridge Institute, University of Southern California, Los Angeles, CA, United States of America.ORCID 0000-0001-8894-9621
Jitin SinglaDepartment of Biosciences and Bioengineering, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, India.ORCID 0000-0001-6225-0783
Liping SuniHuman Institute, ShanghaiTech University, Shanghai, China.ORCID 0000-0002-2420-8936
ShanghaiTech University · CNUniversity of Southern California · USIndian Institute of Technology Roorkee · INLawrence Berkeley National Laboratory · USQB3 · US

Funding

TrainingP41GM103445 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LARABELL, CAROLYN A · 2012 to 2019
$8.2M
User Training and OutreachP30GM138441 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LARABELL, CAROLYN A · 2020 to 2023
$3.7M
NIGMS NIH HHS P30 GM138441NIGMS NIH HHS P41 GM103445
6 · The paper itself

Abstract

Investigating the 3D structures and rearrangements of organelles within a single cell is critical for better characterizing cellular function. Imaging approaches such as soft X-ray tomography have been widely applied to reveal a complex subcellular organization involving multiple inter-organelle interactions. However, 3D segmentation of organelle instances has been challenging despite its importance in organelle characterization. Here we propose an intensity-based post-processing tool to identify and separate organelle instances. Our tool separates sphere-like (insulin vesicle) and columnar-shaped organelle instances (mitochondrion) based on the intensity of raw tomograms, semantic segmentation masks, and organelle morphology. We validate our tool using synthetic tomograms of organelles and experimental tomograms of pancreatic β-cells to separate insulin vesicle and mitochondria instances. As compared to the commonly used connected regions labeling, watershed, and watershed + Gaussian filter methods, our tool results in improved accuracy in identifying organelles in the synthetic tomograms and an improved description of organelle structures in β-cell tomograms. In addition, under different experimental treatment conditions, significant changes in volumes and intensities of both insulin vesicle and mitochondrion are observed in our instance results, revealing their potential roles in maintaining normal β-cell function. Our tool is expected to be applicable for improving the instance segmentation of other images obtained from different cell types using multiple imaging modalities.

Indexed as

Imaging, Three-DimensionalInsulinsOrganellesTomographyX-RaysInsulins

Identifiers

PMID36048824
PMCPMC9436087
OpenAlexW4294043553

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.