Spectral analysis of pair-correlation bandwidth: application to cell biology images

Images from cell biology experiments often indicate the presence of cell clustering, which can provide insight into the mechanisms driving the collective cell behaviour. Pair-correlation functions provide quantitative information about the presence, or absence, of clustering in a spatial distributio...

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Main Authors: Benjamin J. Binder, Matthew J. Simpson
Format: Article
Language:English
Published: The Royal Society 2015-01-01
Series:Royal Society Open Science
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.140494
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author Benjamin J. Binder
Matthew J. Simpson
author_facet Benjamin J. Binder
Matthew J. Simpson
author_sort Benjamin J. Binder
collection DOAJ
description Images from cell biology experiments often indicate the presence of cell clustering, which can provide insight into the mechanisms driving the collective cell behaviour. Pair-correlation functions provide quantitative information about the presence, or absence, of clustering in a spatial distribution of cells. This is because the pair-correlation function describes the ratio of the abundance of pairs of cells, separated by a particular distance, relative to a randomly distributed reference population. Pair-correlation functions are often presented as a kernel density estimate where the frequency of pairs of objects are grouped using a particular bandwidth (or bin width), Δ>0. The choice of bandwidth has a dramatic impact: choosing Δ too large produces a pair-correlation function that contains insufficient information, whereas choosing Δ too small produces a pair-correlation signal dominated by fluctuations. Presently, there is little guidance available regarding how to make an objective choice of Δ. We present a new technique to choose Δ by analysing the power spectrum of the discrete Fourier transform of the pair-correlation function. Using synthetic simulation data, we confirm that our approach allows us to objectively choose Δ such that the appropriately binned pair-correlation function captures known features in uniform and clustered synthetic images. We also apply our technique to images from two different cell biology assays. The first assay corresponds to an approximately uniform distribution of cells, while the second assay involves a time series of images of a cell population which forms aggregates over time. The appropriately binned pair-correlation function allows us to make quantitative inferences about the average aggregate size, as well as quantifying how the average aggregate size changes with time.
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spelling doaj.art-3790e69f3b0f4e0688d15062608114ff2022-12-21T23:39:33ZengThe Royal SocietyRoyal Society Open Science2054-57032015-01-012210.1098/rsos.140494140494Spectral analysis of pair-correlation bandwidth: application to cell biology imagesBenjamin J. BinderMatthew J. SimpsonImages from cell biology experiments often indicate the presence of cell clustering, which can provide insight into the mechanisms driving the collective cell behaviour. Pair-correlation functions provide quantitative information about the presence, or absence, of clustering in a spatial distribution of cells. This is because the pair-correlation function describes the ratio of the abundance of pairs of cells, separated by a particular distance, relative to a randomly distributed reference population. Pair-correlation functions are often presented as a kernel density estimate where the frequency of pairs of objects are grouped using a particular bandwidth (or bin width), Δ>0. The choice of bandwidth has a dramatic impact: choosing Δ too large produces a pair-correlation function that contains insufficient information, whereas choosing Δ too small produces a pair-correlation signal dominated by fluctuations. Presently, there is little guidance available regarding how to make an objective choice of Δ. We present a new technique to choose Δ by analysing the power spectrum of the discrete Fourier transform of the pair-correlation function. Using synthetic simulation data, we confirm that our approach allows us to objectively choose Δ such that the appropriately binned pair-correlation function captures known features in uniform and clustered synthetic images. We also apply our technique to images from two different cell biology assays. The first assay corresponds to an approximately uniform distribution of cells, while the second assay involves a time series of images of a cell population which forms aggregates over time. The appropriately binned pair-correlation function allows us to make quantitative inferences about the average aggregate size, as well as quantifying how the average aggregate size changes with time.https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.140494pair-correlationspectral analysisspatial patternscell clusteringin vitro assay
spellingShingle Benjamin J. Binder
Matthew J. Simpson
Spectral analysis of pair-correlation bandwidth: application to cell biology images
Royal Society Open Science
pair-correlation
spectral analysis
spatial patterns
cell clustering
in vitro assay
title Spectral analysis of pair-correlation bandwidth: application to cell biology images
title_full Spectral analysis of pair-correlation bandwidth: application to cell biology images
title_fullStr Spectral analysis of pair-correlation bandwidth: application to cell biology images
title_full_unstemmed Spectral analysis of pair-correlation bandwidth: application to cell biology images
title_short Spectral analysis of pair-correlation bandwidth: application to cell biology images
title_sort spectral analysis of pair correlation bandwidth application to cell biology images
topic pair-correlation
spectral analysis
spatial patterns
cell clustering
in vitro assay
url https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.140494
work_keys_str_mv AT benjaminjbinder spectralanalysisofpaircorrelationbandwidthapplicationtocellbiologyimages
AT matthewjsimpson spectralanalysisofpaircorrelationbandwidthapplicationtocellbiologyimages