Evidence map›Paper›PMID 36345757›Full record

ArticleJournal of synchrotron radiation2022

ROI-Finder: machine learning to guide region-of-interest scanning for X-ray fluorescence microscopy.

M A Z Chowdhury, K Ok, Y Luo, Z Liu, S Chen, T V O'Halloran, R Kettimuthu, A Tekawade

Abstract read
In one paragraph

Article in Journal of synchrotron radiation, 2022. 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
–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

2 citing papers in PubMed.

  1. Distinguishing isotropic and anisotropic signals for X-ray total scattering using machine learning.Acta crystallographica. Section A, Foundations and advances · 2025
    Article
  2. 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

8 authors.

M A Z ChowdhuryData Science and Learning Division, Argonne National Laboratory, Lemont, IL 60439, USA.
K OkDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA.
Y LuoX-ray Science Division, Argonne National Laboratory, Lemont, IL 60439, USA.
Z LiuData Science and Learning Division, Argonne National Laboratory, Lemont, IL 60439, USA.ORCID 0000-0002-6647-4423
S ChenX-ray Science Division, Argonne National Laboratory, Lemont, IL 60439, USA.
T V O'HalloranDepartment of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA.
R KettimuthuData Science and Learning Division, Argonne National Laboratory, Lemont, IL 60439, USA.
A TekawadeData Science and Learning Division, Argonne National Laboratory, Lemont, IL 60439, USA.

Funding

TR&D Project 3: Photoacoustic Detection of Metal Fluxes at the Tissue LevelP41GM135018 · NIGMS · NORTHWESTERN UNIVERSITY · PI JACOBSEN, CHRIS JOHNSON, O'HALLORAN, THOMAS V · 2020 to 2024
$5.8M
METALLOREGULATION BY MERR AND FUR PROTEIN FAMILIESR37GM038784 · NIGMS · NORTHWESTERN UNIVERSITY · PI O'HALLORAN, THOMAS V · 2001 to 2010
$3.6M
Metalloregulation by MerR and Fur Protein FamiliesR01GM038784 · NIGMS · NORTHWESTERN UNIVERSITY · PI O'HALLORAN, THOMAS V · 1992 to 2025
$3.5M
MECHANISTIC STUDY OF THE MERR METALLOREGULATORY PROTEINR29GM038784 · NIGMS · NORTHWESTERN UNIVERSITY · PI O'HALLORAN, THOMAS V · 1987 to 1991
–
Argonne National Laboratory LDRD PRJ1008073Argonne National Laboratory LDRD PRJ1008870NIGMS NIH HHS P41 GM135018NIGMS NIH HHS R01 GM038784NIGMS NIH HHS R37 GM038784NIH HHS ARRA S10 SP0007167NIH HHS GM038784NIH HHS P41GM181350US Department of Energy, Office of Science DE-AC02-06CH1135US Department of Energy, Office of Science PRJ1009594
6 · The paper itself

Abstract

The microscopy research at the Bionanoprobe (currently at beamline 9-ID and later 2-ID after APS-U) of Argonne National Laboratory focuses on applying synchrotron X-ray fluorescence (XRF) techniques to obtain trace elemental mappings of cryogenic biological samples to gain insights about their role in critical biological activities. The elemental mappings and the morphological aspects of the biological samples, in this instance, the bacterium Escherichia coli (E. Coli), also serve as label-free biological fingerprints to identify E. coli cells that have been treated differently. The key limitations of achieving good identification performance are the extraction of cells from raw XRF measurements via binary conversion, definition of features, noise floor and proportion of cells treated differently in the measurement. Automating cell extraction from raw XRF measurements across different types of chemical treatment and the implementation of machine-learning models to distinguish cells from the background and their differing treatments are described. Principal components are calculated from domain knowledge specific features and clustered to distinguish healthy and poisoned cells from the background without manual annotation. The cells are ranked via fuzzy clustering to recommend regions of interest for automated experimentation. The effects of dwell time and the amount of data required on the usability of the software are also discussed.

Indexed as

Escherichia coliSynchrotronsMachine LearningMicroscopy, FluorescenceX-RaysE. colifuzzy clusteringlive cell imagingmicroscopyprincipal components analysisregion-of-interest detectionX-ray fluorescence

Identifiers

PMID36345757
PMCPMC9641565

What OpenQuestion holds

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Registered trials

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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.