Evidence map›Paper›PMID 36303727›Full record

ReviewFrontiers in bioinformatics2021

Efficient Cross-Correlation Filtering of One- and Two-Color Single Molecule Localization Microscopy Data.

Angel Mancebo, Dushyant Mehra, Chiranjib Banerjee, Do-Hyung Kim, Elias M Puchner

Abstract readReview
In one paragraph

Review in Frontiers in bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

5 authors.

Angel ManceboSchool of Physics and Astronomy, University of Minnesota, Minneapolis, MN, United States.
Dushyant MehraSchool of Physics and Astronomy, University of Minnesota, Minneapolis, MN, United States.
Chiranjib BanerjeeSchool of Physics and Astronomy, University of Minnesota, Minneapolis, MN, United States.
Do-Hyung KimDepartment of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, Minneapolis, MN, United States.
Elias M PuchnerSchool of Physics and Astronomy, University of Minnesota, Minneapolis, MN, United States.

Funding

Mechanisms of mTORC1 signaling to protein degradation pathwaysR35GM130353 · NIGMS · UNIVERSITY OF MINNESOTA · PI Do-Hyung Kim · 2019 to 2026
$4.2M
Developing Diffusion-Contrast Super-Resolution Microscopy to Study Protein Interactions at Extreme Concentration Ratios in Live CellsR21GM127965 · NIGMS · UNIVERSITY OF MINNESOTA · PI PUCHNER, GEORG ELIAS MICHAEL · 2018 to 2019
$283k
NIGMS NIH HHS R21 GM127965NIGMS NIH HHS R35 GM130353
6 · The paper itself

Abstract

Single molecule localization microscopy has become a prominent technique to quantitatively study biological processes below the optical diffraction limit. By fitting the intensity profile of single sparsely activated fluorophores, which are often attached to a specific biomolecule within a cell, the locations of all imaged fluorophores are obtained with ∼20 nm resolution in the form of a coordinate table. While rendered super-resolution images reveal structural features of intracellular structures below the optical diffraction limit, the ability to further analyze the molecular coordinates presents opportunities to gain additional quantitative insights into the spatial distribution of a biomolecule of interest. For instance, pair-correlation or radial distribution functions are employed as a measure of clustering, and cross-correlation analysis reveals the colocalization of two biomolecules in two-color SMLM data. Here, we present an efficient filtering method for SMLM data sets based on pair- or cross-correlation to isolate localizations that are clustered or appear in proximity to a second set of localizations in two-color SMLM data. In this way, clustered or colocalized localizations can be separately rendered and analyzed to compare other molecular properties to the remaining localizations, such as their oligomeric state or mobility in live cell experiments. Current matrix-based cross-correlation analyses of large data sets quickly reach the limitations of computer memory due to the space complexity of constructing the distance matrices. Our approach leverages k-dimensional trees to efficiently perform range searches, which dramatically reduces memory needs and the time for the analysis. We demonstrate the versatile applications of this method with simulated data sets as well as examples of two-color SMLM data. The provided MATLAB code and its description can be integrated into existing localization analysis packages and provides a useful resource to analyze SMLM data with new detail.

Indexed as

clusteringcolocalizationcross-correlationphoto-activated localization microscopysingle-molecule localization microscopy

Identifiers

PMID36303727
PMCPMC9581065

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.