Evidence map›Paper›PMID 34107436›Full record

ArticleComputers in biology and medicine2021

ASIST: Annotation-free synthetic instance segmentation and tracking by adversarial simulations.

Quan Liu, Isabella M Gaeta, Mengyang Zhao, Ruining Deng, Aadarsh Jha, Bryan A Millis, Anita Mahadevan-Jansen, Matthew J Tyska, Yuankai Huo

Abstract read
In one paragraph

Article in Computers in biology and medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

2 citing papers in PubMed.

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4 · The record

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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

9 authors.

Quan LiuVanderbilt University, Computer Science, Nashville, TN, 37215, USA.
Isabella M GaetaVanderbilt University, Cell and Developmental Biology, Nashville, TN, 37215, USA.
Mengyang ZhaoTufts University, Computer Science, Medford, MA, 02155, USA.
Ruining DengVanderbilt University, Computer Science, Nashville, TN, 37215, USA.
Aadarsh JhaVanderbilt University, Computer Science, Nashville, TN, 37215, USA.
Bryan A MillisVanderbilt University, Cell and Developmental Biology, Nashville, TN, 37215, USA.
Anita Mahadevan-JansenVanderbilt University, Biomedical Engineering, Nashville, TN, 37215, USA.
Matthew J TyskaVanderbilt University, Cell and Developmental Biology, Nashville, TN, 37215, USA.
Yuankai HuoVanderbilt University, Computer Science, Nashville, TN, 37215, USA. Electronic address: yuankai.huo@vanderbilt.edu.

Funding

TRAINING PROGRAM IN CELLULAR, BIOCHEMICAL, &MOLECULAR ST32GM008554 · NIGMS · VANDERBILT UNIVERSITY · PI PATTON, JAMES G. · 1995 to 2020
$7.4M
Molecular basis of brush border assemblyR01DK095811 · NIDDK · VANDERBILT UNIVERSITY · PI MATTHEW J TYSKA · 2013 to 2026
$4.9M
Role of I-BAR proteins in enterocyte differentiationR01DK111949 · NIDDK · VANDERBILT UNIVERSITY · PI MATTHEW J TYSKA · 2017 to 2026
$4.2M
Myosin-2 function in the enterocyte terminal webR01DK125546 · NIDDK · VANDERBILT UNIVERSITY · PI TYSKA, MATTHEW J · 2021 to 2024
$1.4M
Investigating the role of EPS8 in microvillar growthF31DK122692 · NIDDK · VANDERBILT UNIVERSITY · PI GAETA, ISABELLA M · 2019 to 2021
$91k
NIDDK NIH HHS F31 DK122692NIDDK NIH HHS R01 DK095811NIDDK NIH HHS R01 DK111949NIDDK NIH HHS R01 DK125546NIGMS NIH HHS T32 GM008554
6 · The paper itself

Abstract

backgroundThe quantitative analysis of microscope videos often requires instance segmentation and tracking of cellular and subcellular objects. The traditional method consists of two stages: (1) performing instance object segmentation of each frame, and (2) associating objects frame-by-frame. Recently, pixel-embedding-based deep learning approaches these two steps simultaneously as a single stage holistic solution. Pixel-embedding-based learning forces similar feature representation of pixels from the same object, while maximizing the difference of feature representations from different objects. However, such deep learning methods require consistent annotations not only spatially (for segmentation), but also temporally (for tracking). In computer vision, annotated training data with consistent segmentation and tracking is resource intensive, the severity of which is multiplied in microscopy imaging due to (1) dense objects (e.g., overlapping or touching), and (2) high dynamics (e.g., irregular motion and mitosis). Adversarial simulations have provided successful solutions to alleviate the lack of such annotations in dynamics scenes in computer vision, such as using simulated environments (e.g., computer games) to train real-world self-driving systems.

methodsIn this paper, we propose an annotation-free synthetic instance segmentation and tracking (ASIST) method with adversarial simulation and single-stage pixel-embedding based learning. CONTRIBUTION: The contribution of this paper is three-fold: (1) the proposed method aggregates adversarial simulations and single-stage pixel-embedding based deep learning (2) the method is assessed with both the cellular (i.e., HeLa cells); and subcellular (i.e., microvilli) objects; and (3) to the best of our knowledge, this is the first study to explore annotation-free instance segmentation and tracking study for microscope videos.

resultsThe ASIST method achieved an important step forward, when compared with fully supervised approaches: ASIST shows 7%-11% higher segmentation, detection and tracking performance on microvilli relative to fully supervised methods, and comparable performance on Hela cell videos.

Indexed as

Image Processing, Computer-AssistedMicroscopyComputer SimulationHeLa CellsHumansAnnotation freeCellularSegmentationSubcelluarTracking

Identifiers

PMID34107436
PMCPMC8263511

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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.