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Capturing single-cell heterogeneity via data fusion improves image-based profiling | Nature Communications

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data-article-title="">Capturing single-cell heterogeneity via data fusion improves image-based profiling</h1> <ul class="c-article-author-list c-article-author-list--short" data-test="authors-list" data-component-authors-activator="authors-list"><li class="c-article-author-list__item"><a data-test="author-name" data-track="click" data-track-action="open author" data-track-label="link" href="#auth-Mohammad_H_-Rohban-Aff1-Aff2" data-author-popup="auth-Mohammad_H_-Rohban-Aff1-Aff2" data-author-search="Rohban, Mohammad H." data-corresp-id="c1">Mohammad H. Rohban<svg width="16" height="16" focusable="false" role="img" aria-hidden="true" class="u-icon"><use xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#icon-eds-i-mail-medium"></use></svg></a><sup class="u-js-hide"><a href="#Aff1">1</a>,<a href="#Aff2">2</a></sup>, </li><li class="c-article-author-list__item"><a data-test="author-name" data-track="click" data-track-action="open author" data-track-label="link" href="#auth-Hamdah_S_-Abbasi-Aff1" data-author-popup="auth-Hamdah_S_-Abbasi-Aff1" data-author-search="Abbasi, Hamdah S.">Hamdah S. Abbasi</a><sup class="u-js-hide"><a href="#Aff1">1</a></sup>, </li><li class="c-article-author-list__item c-article-author-list__item--hide-small-screen"><a data-test="author-name" data-track="click" data-track-action="open author" data-track-label="link" href="#auth-Shantanu-Singh-Aff1" data-author-popup="auth-Shantanu-Singh-Aff1" data-author-search="Singh, Shantanu">Shantanu Singh</a><span class="u-js-hide">  <a class="js-orcid" href="http://orcid.org/0000-0003-3150-3025"><span class="u-visually-hidden">ORCID: </span>orcid.org/0000-0003-3150-3025</a></span><sup class="u-js-hide"><a href="#Aff1">1</a></sup> &amp; </li><li class="c-article-author-list__show-more" aria-label="Show all 4 authors for this article" title="Show all 4 authors for this article">…</li><li class="c-article-author-list__item"><a data-test="author-name" data-track="click" data-track-action="open author" data-track-label="link" href="#auth-Anne_E_-Carpenter-Aff1" data-author-popup="auth-Anne_E_-Carpenter-Aff1" data-author-search="Carpenter, Anne E.">Anne E. Carpenter</a><span class="u-js-hide">  <a class="js-orcid" href="http://orcid.org/0000-0003-1555-8261"><span class="u-visually-hidden">ORCID: </span>orcid.org/0000-0003-1555-8261</a></span><sup class="u-js-hide"><a href="#Aff1">1</a></sup> </li></ul><button aria-expanded="false" class="c-article-author-list__button"><svg width="16" height="16" focusable="false" role="img" aria-hidden="true" class="u-icon"><use xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#icon-eds-i-chevron-down-medium"></use></svg><span>Show authors</span></button> <p class="c-article-info-details" data-container-section="info"> <a data-test="journal-link" href="/ncomms" data-track="click" data-track-action="journal homepage" data-track-category="article body" data-track-label="link"><i data-test="journal-title">Nature Communications</i></a> <b data-test="journal-volume"><span class="u-visually-hidden">volume</span> 10</b>, Article number: <span data-test="article-number">2082</span> (<span data-test="article-publication-year">2019</span>) <a href="#citeas" class="c-article-info-details__cite-as u-hide-print" data-track="click" data-track-action="cite this article" data-track-label="link">Cite this article</a> </p> <div class="c-article-metrics-bar__wrapper u-clear-both"> <ul class="c-article-metrics-bar u-list-reset"> <li class=" c-article-metrics-bar__item" data-test="access-count"> <p class="c-article-metrics-bar__count">7584 <span class="c-article-metrics-bar__label">Accesses</span></p> </li> <li class="c-article-metrics-bar__item" data-test="citation-count"> <p class="c-article-metrics-bar__count">24 <span class="c-article-metrics-bar__label">Citations</span></p> </li> <li class="c-article-metrics-bar__item" data-test="altmetric-score"> <p class="c-article-metrics-bar__count">11 <span class="c-article-metrics-bar__label">Altmetric</span></p> </li> <li class="c-article-metrics-bar__item"> <p class="c-article-metrics-bar__details"><a href="/articles/s41467-019-10154-8/metrics" data-track="click" data-track-action="view metrics" data-track-label="link" rel="nofollow">Metrics <span class="u-visually-hidden">details</span></a></p> </li> </ul> </div> </header> <div class="u-js-hide" data-component="article-subject-links"> <h3 class="c-article__sub-heading">Subjects</h3> <ul class="c-article-subject-list"> <li class="c-article-subject-list__subject"><a href="/subjects/data-mining" data-track="click" data-track-action="view subject" data-track-label="link">Data mining</a></li><li class="c-article-subject-list__subject"><a href="/subjects/high-throughput-screening" data-track="click" data-track-action="view subject" data-track-label="link">High-throughput screening</a></li><li class="c-article-subject-list__subject"><a href="/subjects/statistical-methods" data-track="click" data-track-action="view subject" data-track-label="link">Statistical methods</a></li> </ul> </div> </div> <div class="c-article-body"> <section aria-labelledby="Abs1" data-title="Abstract" lang="en"><div class="c-article-section" id="Abs1-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="Abs1">Abstract</h2><div class="c-article-section__content" id="Abs1-content"><p>Single-cell resolution technologies warrant computational methods that capture cell heterogeneity while allowing efficient comparisons of populations. Here, we summarize cell populations by adding features’ dispersion and covariances to population averages, in the context of image-based profiling. We find that data fusion is critical for these metrics to improve results over the prior alternatives, providing at least ~20% better performance in predicting a compound’s mechanism of action (MoA) and a gene’s pathway.</p></div></div></section> <noscript> </noscript> <section aria-labelledby="inline-recommendations" data-title="Inline Recommendations" class="c-article-recommendations" data-track-component="inline-recommendations"> <h3 class="c-article-recommendations-title" id="inline-recommendations">Similar content being viewed by others</h3> <div class="c-article-recommendations-list"> <div class="c-article-recommendations-list__item"> <article class="c-article-recommendations-card" itemscope itemtype="http://schema.org/ScholarlyArticle"> <div class="c-article-recommendations-card__img"><img src="https://media.springernature.com/w215h120/springer-static/image/art%3A10.1038%2Fs41587-021-00895-7/MediaObjects/41587_2021_895_Fig1_HTML.png" loading="lazy" alt=""></div> <div class="c-article-recommendations-card__main"> <h3 class="c-article-recommendations-card__heading" itemprop="name headline"> <a class="c-article-recommendations-card__link" itemprop="url" href="https://www.nature.com/articles/s41587-021-00895-7?fromPaywallRec=false" data-track="select_recommendations_1" data-track-context="inline recommendations" data-track-action="click recommendations inline - 1" data-track-label="10.1038/s41587-021-00895-7">Computational principles and challenges in single-cell data integration </a> </h3> <div class="c-article-meta-recommendations" data-test="recommendation-info"> <span class="c-article-meta-recommendations__item-type">Article</span> <span class="c-article-meta-recommendations__date">03 May 2021</span> </div> </div> </article> </div> <div class="c-article-recommendations-list__item"> <article class="c-article-recommendations-card" itemscope itemtype="http://schema.org/ScholarlyArticle"> <div class="c-article-recommendations-card__img"><img src="https://media.springernature.com/w215h120/springer-static/image/art%3A10.1038%2Fs42003-022-04343-3/MediaObjects/42003_2022_4343_Fig1_HTML.png" loading="lazy" alt=""></div> <div class="c-article-recommendations-card__main"> <h3 class="c-article-recommendations-card__heading" itemprop="name headline"> <a class="c-article-recommendations-card__link" itemprop="url" href="https://www.nature.com/articles/s42003-022-04343-3?fromPaywallRec=false" data-track="select_recommendations_2" data-track-context="inline recommendations" data-track-action="click recommendations inline - 2" data-track-label="10.1038/s42003-022-04343-3">A statistical framework for high-content phenotypic profiling using cellular feature distributions </a> </h3> <div class="c-article-meta-recommendations" data-test="recommendation-info"> <span class="c-article-meta-recommendations__item-type">Article</span> <span class="c-article-meta-recommendations__access-type">Open access</span> <span class="c-article-meta-recommendations__date">22 December 2022</span> </div> </div> </article> </div> <div class="c-article-recommendations-list__item"> <article class="c-article-recommendations-card" itemscope itemtype="http://schema.org/ScholarlyArticle"> <div class="c-article-recommendations-card__img"><img src="https://media.springernature.com/w215h120/springer-static/image/art%3A10.1038%2Fs12276-024-01186-2/MediaObjects/12276_2024_1186_Fig1_HTML.png" loading="lazy" alt=""></div> <div class="c-article-recommendations-card__main"> <h3 class="c-article-recommendations-card__heading" itemprop="name headline"> <a class="c-article-recommendations-card__link" itemprop="url" href="https://www.nature.com/articles/s12276-024-01186-2?fromPaywallRec=false" data-track="select_recommendations_3" data-track-context="inline recommendations" data-track-action="click recommendations inline - 3" data-track-label="10.1038/s12276-024-01186-2">Advances in single-cell omics and multiomics for high-resolution molecular profiling </a> </h3> <div class="c-article-meta-recommendations" data-test="recommendation-info"> <span class="c-article-meta-recommendations__item-type">Article</span> <span class="c-article-meta-recommendations__access-type">Open access</span> <span class="c-article-meta-recommendations__date">05 March 2024</span> </div> </div> </article> </div> </div> </section> <script> window.dataLayer = window.dataLayer || []; window.dataLayer.push({ recommendations: { recommender: 'semantic', model: 'specter', policy_id: 'NA', timestamp: 1732666216, embedded_user: 'null' } }); </script> <div class="main-content"> <section data-title="Introduction"><div class="c-article-section" id="Sec1-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="Sec1">Introduction</h2><div class="c-article-section__content" id="Sec1-content"><p>As a very early large-scale, high-dimensional, single-cell-resolution data type, high-throughput microscopy experiments have presented one of the first exemplars of the challenges in summarizing and comparing cell populations.</p><p>One of the key challenges is creating a profile of each cell population. A profile is a summary of many features of a population that enables efficient comparison with other populations while simultaneously capturing their natural variations and possible subpopulations. Recent studies have yielded many insights into cellular heterogeneity and its importance<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" title="Janes, K. A. Single-cell states versus single-cell atlases—two classes of heterogeneity that differ in meaning and method. Curr. Opin. Biotechnol. 39, 120–125 (2016)." href="#ref-CR1" id="ref-link-section-d52554175e365">1</a>,<a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" title="Altschuler, S. J. &amp; Wu, L. F. Cellular heterogeneity: do differences make a difference? Cell 141, 559–563 (2010)." href="#ref-CR2" id="ref-link-section-d52554175e365_1">2</a>,<a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" title="Pelkmans, L. Cell Biology. Using cell-to-cell variability—a new era in molecular biology. Science 336, 425–426 (2012)." href="#ref-CR3" id="ref-link-section-d52554175e365_2">3</a>,<a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 4" title="Deb, D. et al. Combination therapy targeting BCL6 and phospho-STAT3 defeats intratumor heterogeneity in a subset of non–small cell lung cancers. Cancer Res. 77, 3070–3081 (2017)." href="/articles/s41467-019-10154-8#ref-CR4" id="ref-link-section-d52554175e368">4</a></sup>.</p><p>Although anecdotal evidence of the value of capturing heterogeneity abounds, it has remained puzzling that so-called average profiling, the practice of feature-averaging all single-cell measurements together using measures-of-center (mean or median), has remained the top-ranked approach in the field of image-based (or morphological) profiling, whether those features are raw or pre-processed using unsupervised learning, or whether they derive from classical image processing or deep learning.</p><p>In image-based profiling, average profiling has been used as a straightforward way of summarizing a cell population (a sample) into a fixed length vector (a sample’s profile), with one value per feature per sample. Various metrics of similarity between profiles of two samples can then be used to infer whether they show similar phenotypic responses to their respective treatments. Average profiling typically results in a thousand-fold decrease in data size (because there are typically around a thousand cells per well in image-based profiling experiments conducted in multi-well plates), which makes downstream processing both computationally manageable and potentially statistically more robust.</p><p>However, average profiling results in loss of information about a population’s heterogeneity. The information loss can manifest in different forms. For example, multiple configurations of distinct subpopulations of cells could yield identical average profiles. Or, if two subpopulations with opposite phenotypes exist in a sample, they might cancel out yielding a profile indistinguishable from that of a sample that contains neither subpopulation. In addition to information loss, averaging can result in misleading interpretation of feature associations, e.g., Simpson’s paradox<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 5" title="Trapnell, C. Defining cell types and states with single-cell genomics. Genome Res. 25, 1491–1498 (2015)." href="/articles/s41467-019-10154-8#ref-CR5" id="ref-link-section-d52554175e382">5</a></sup>. Finally, averaging makes the implicit assumption that the joint distribution of the underlying features is unimodal, which if violated can lead to artifacts. In this paper we investigate whether including heterogeneity measures in the profiles of cells undergoing various treatment conditions can improve upon prior methods that do not capture heterogeneity well.</p><p>Several methods have been developed in an attempt to capture cell population heterogeneity while still allowing efficient comparisons between different populations. A simple solution is to compute the cell population’s dispersion (e.g., standard deviation or median absolute deviation, MAD) for each feature and concatenate these values with the average profile. Although feature normalization brings features to comparable scales, features in average profiles generally follow a probability distribution different from that of the features in dispersion-based profiles. This discrepancy may lead to the correlation between profiles being biased toward either only features of the average or the dispersion. Concatenation can also dilute the signal-to-noise ratio (SNR) if one type of profile already has a low SNR<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 6" title="Wang, B. et al. Similarity network fusion for aggregating data types on a genomic scale. Nat. Methods 11, 333–337 (2014)." href="/articles/s41467-019-10154-8#ref-CR6" id="ref-link-section-d52554175e389">6</a></sup>, i.e., the SNR of concatenated data would be lower than the maximum of SNRs across data types. In practice, concatenation of median and MAD profiles has been shown to provide only a minor improvement over median profiling alone<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e393">7</a></sup>.</p><p>Measures of dispersion might only capture a small fraction of the heterogeneity in the data, i.e., they disregard subpopulation structures, because they involve processing each feature separately. Instead of capturing dispersion for each individual feature, one can alternatively model the heterogeneity by clustering cells using all features simultaneously. In this approach, a subset of data is used to estimate clusters of cells (representing subpopulations) and profiles are calculated as the feature averages within subpopulations<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 8" title="Loo, L.-H. et al. An approach for extensibly profiling the molecular states of cellular subpopulations. Nat. Methods 6, 759–765 (2009)." href="/articles/s41467-019-10154-8#ref-CR8" id="ref-link-section-d52554175e400">8</a></sup>. Alternatively, cells can be classified into pre-determined phenotype classes using a supervised approach, and the profile is then defined as the fraction of cells in each phenotype class<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 9" title="Fuchs, F. et al. Clustering phenotype populations by genome-wide RNAi and multiparametric imaging. Mol. Syst. Biol. 6, 370 (2010)." href="/articles/s41467-019-10154-8#ref-CR9" id="ref-link-section-d52554175e404">9</a></sup>. However, many cell phenotypes are better considered as a continuum of varying morphologies rather than discrete populations. Further, there may exist some rare subpopulations that are unique to a small portion of the data that may be overlooked in the clustering step. As a remedy, if we instead try to cluster each sample separately, the subpopulations may not be appropriately matched across samples, which makes the profiles uncomparable across the samples. Unfortunately, despite their intuitive appeal, none of these ideas have proven to significantly improve upon the baseline average profiling, at least, on the single public dataset with available ground truth, which are annotations of the mechanism of action (MOA) of a small set of compounds. In a comparison of profiling methods, average profiling (after dimensionality reduction) outperformed methods that attempted to capture heterogeneity in the data<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e408">7</a></sup>. More recent work demonstrated a deep learning approach to feature extraction that yielded the highest performance yet, but nonetheless relied on average profiling<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 10" title="Michael Ando, D., McLean, C. &amp; Berndl, M. Improving phenotypic measurements in high-content imaging screens. bioRxiv 161422 preprint at &#xA; https://www.biorxiv.org/content/10.1101/161422v1&#xA; &#xA; (2017)." href="/articles/s41467-019-10154-8#ref-CR10" id="ref-link-section-d52554175e412">10</a></sup>.</p><p>Here, we test fusing information from the dispersion profiles with the average profiles at the level of profiles’ similarity matrices. This avoids inclusion of features with inherently different probability densities in the final profile. Modeling profile similarity matrices from disparate data types using a graph has been shown to be effective in handling heterogeneous data sources such as DNA methylation, miRNA expression, and mRNA expression<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 6" title="Wang, B. et al. Similarity network fusion for aggregating data types on a genomic scale. Nat. Methods 11, 333–337 (2014)." href="/articles/s41467-019-10154-8#ref-CR6" id="ref-link-section-d52554175e419">6</a></sup>.</p><p>We also consider alternate heterogeneity representations that do not explicitly model subpopulation information, but nevertheless capture heterogeneity. Higher order moments, which consider combinations of features (as opposed to univariate moments of single features such as mean/median or standard deviations) are excellent candidates. As shown schematically (Fig. <a data-track="click" data-track-label="link" data-track-action="figure anchor" href="/articles/s41467-019-10154-8#Fig1">1</a>), two cell populations may differ dramatically but have identical means and standard deviations. However, there is a substantial difference in the covariance (a second moment) of two features between the control (on the left) and treatment (on the right) cell populations, making this information useful to include in the populations’ profiles.</p><div class="c-article-section__figure js-c-reading-companion-figures-item" data-test="figure" data-container-section="figure" id="figure-1" data-title="Fig. 1"><figure><figcaption><b id="Fig1" class="c-article-section__figure-caption" data-test="figure-caption-text">Fig. 1</b></figcaption><div class="c-article-section__figure-content"><div class="c-article-section__figure-item"><a class="c-article-section__figure-link" data-test="img-link" data-track="click" data-track-label="image" data-track-action="view figure" href="/articles/s41467-019-10154-8/figures/1" rel="nofollow"><picture><source type="image/webp" srcset="//media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-019-10154-8/MediaObjects/41467_2019_10154_Fig1_HTML.png?as=webp"><img aria-describedby="Fig1" src="//media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-019-10154-8/MediaObjects/41467_2019_10154_Fig1_HTML.png" alt="figure 1" loading="lazy" width="685" height="624"></picture></a></div><div class="c-article-section__figure-description" data-test="bottom-caption" id="figure-1-desc"><p>Features’ covariance can capture cell phenotypes better than feature averages or dispersion. In this synthetic example, the negative control sample (on the left) consists of cells displaying heterogeneous morphologies. The treatment, on the other hand, shows two distinct subpopulations. In both cases, the scatter plot helps to see that the mean and standard deviation of both measured cell features (area and elongation) are equivalent in the two cases. However, the two features positively correlate in the treatment condition as opposed to the control. In such a case, the covariance can distinguish the phenotypes better than simple averages (e.g., means and medians) and measures of dispersion (e.g., standard deviations and median absolute deviations)</p></div></div><div class="u-text-right u-hide-print"><a class="c-article__pill-button" data-test="article-link" data-track="click" data-track-label="button" data-track-action="view figure" href="/articles/s41467-019-10154-8/figures/1" data-track-dest="link:Figure1 Full size image" aria-label="Full size image figure 1" rel="nofollow"><span>Full size image</span><svg width="16" height="16" focusable="false" role="img" aria-hidden="true" class="u-icon"><use xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#icon-eds-i-chevron-right-small"></use></svg></a></div></figure></div><p>We also motivate the use of higher order joint statistical moments for profiling from a more theoretical standpoint. In the terminology of estimation theory, we aim to find a sufficient statistic for the unknown subpopulations to serve as the sample profile. A sufficient statistic is a summary of data that provides maximal information about the unknown parameters of a model that is used to explain the data. Previous work has shown that under certain assumptions, the first, second, and third order moments, collectively, are approximately a sufficient statistic for modeling subpopulations given a large enough sample size<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 11" title="Hsu, D. &amp; Kakade, S. M. Learning Mixtures of Spherical Gaussians: Moment Methods and Spectral Decompositions. In Proc. 4th Conference on Innovations in Theoretical Computer Science 11–20 (ACM, Berkeley, CA, USA 2013)." href="/articles/s41467-019-10154-8#ref-CR11" id="ref-link-section-d52554175e449">11</a></sup> (Methods). Unfortunately, for typical single-cell datasets, sample sizes are too small, and computational requirements are too high, for estimating third order moments.</p><p>Here we find that even sparse random projections<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 12" title="Li, P., Hastie, T. J. &amp; Church, K. W. Very Sparse Random Projections. In Proc. 12th ACM SIGKDD International Conference on Knowledge Discovery and Data Mining 287–296 (ACM, Philadelphia, PA, USA 2006)." href="/articles/s41467-019-10154-8#ref-CR12" id="ref-link-section-d52554175e457">12</a></sup> of covariances (second-order moments) can provide a substantial improvement in the ability to accurately compare cell populations for phenotypic similarity, when combined with median and MAD profiles via data fusion.</p><p>Testing profiling methods against each other is not a trivial exercise, given that the true similarities and differences among large sets of cell populations is rarely known. We therefore tested the approach on three different publicly available datasets where some ground truth (i.e., expected results), albeit imperfect, is known. Cell measurements in the datasets are based on Cell Painting, which is an image-based assay designed to capture cell morphology<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 13" title="Bray, M.-A. et al. Cell Painting, a high-content image-based assay for morphological profiling using multiplexed fluorescent dyes. Nat. Protoc. 11, 1757–1774 (2016)." href="/articles/s41467-019-10154-8#ref-CR13" id="ref-link-section-d52554175e464">13</a></sup>. For these benchmark datasets, our laboratory had released the image data<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 14" title="Gustafsdottir, S. M. et al. Multiplex cytological profiling assay to measure diverse cellular states. PLoS One 8, e80999 (2013)." href="/articles/s41467-019-10154-8#ref-CR14" id="ref-link-section-d52554175e468">14</a>,<a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 15" title="Bray, M.-A. et al. A dataset of images and morphological profiles of 30 000 small-molecule treatments using the Cell Painting assay. Gigascience 6, 1–5 (2017)." href="/articles/s41467-019-10154-8#ref-CR15" id="ref-link-section-d52554175e471">15</a></sup> but for this study we collected ground truth to create a proper testing scenario. We used datasets that had a sufficient number of perturbations for the data fusion technique to work (Methods), and therefore did not include the dataset reported in a previously published study<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e475">7</a></sup>.</p><p>To summarize, to account for the single-cell heterogeneity in comparing cell populations, we propose to fuse information from average, dispersion, and randomly projected covariance profiles at the level of profiles’ similarity matrices. On three new benchmark datasets, the resulting fused similarity matrix shows significant improvement of concordance to the known ground truth compared to similarity matrices that are based on each type of profile alone, and some methods that were previously proposed to capture population heterogeneity.</p></div></div></section><section data-title="Results"><div class="c-article-section" id="Sec2-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="Sec2">Results</h2><div class="c-article-section__content" id="Sec2-content"><h3 class="c-article__sub-heading" id="Sec3">Fused profile similarities improves performance</h3><p>To evaluate each profiling method, we tested whether pairs of cell populations that look most alike, according to the computed image-based profiles, have been treated with perturbations that are annotated as having the same mechanism of action (for compounds) or the same pathway (for gene overexpressions). Similarity between pairs of image-based profiles are established based on the profiles’ correlation (Methods).</p><p>We find that the enrichment of top-correlated perturbation pairs, whether genetic or chemical, in having the same mechanism of action or the same pathway (Methods), is improved when median absolute deviation and/or covariances are combined with the median profiles through Similarity Network Fusion (SNF) (Methods) (Fig. <a data-track="click" data-track-label="link" data-track-action="figure anchor" href="/articles/s41467-019-10154-8#Fig2">2a</a> and Supplementary Tables <a data-track="click" data-track-label="link" data-track-action="supplementary material anchor" href="/articles/s41467-019-10154-8#MOESM1">1</a> and <a data-track="click" data-track-label="link" data-track-action="supplementary material anchor" href="/articles/s41467-019-10154-8#MOESM1">2</a>). Covariances are summarized by sparse random projections to avoid the curse of dimensionality. The enrichment score we use here is appropriate for applications where the aim is to identify the most highly correlated treatment pairs rather than to classify every treatment into a class<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e506">7</a></sup>. Examples in drug discovery include lead-hopping, identifying gene function, and matching genetic and chemical perturbations. An increase in enrichment score would directly translate to a proportional increase in the chances of finding a novel connections between genes, compounds, and diseases.</p><div class="c-article-section__figure js-c-reading-companion-figures-item" data-test="figure" data-container-section="figure" id="figure-2" data-title="Fig. 2"><figure><figcaption><b id="Fig2" class="c-article-section__figure-caption" data-test="figure-caption-text">Fig. 2</b></figcaption><div class="c-article-section__figure-content"><div class="c-article-section__figure-item"><a class="c-article-section__figure-link" data-test="img-link" data-track="click" data-track-label="image" data-track-action="view figure" href="/articles/s41467-019-10154-8/figures/2" rel="nofollow"><picture><source type="image/webp" srcset="//media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-019-10154-8/MediaObjects/41467_2019_10154_Fig2_HTML.png?as=webp"><img aria-describedby="Fig2" src="//media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-019-10154-8/MediaObjects/41467_2019_10154_Fig2_HTML.png" alt="figure 2" loading="lazy" width="685" height="575"></picture></a></div><div class="c-article-section__figure-description" data-test="bottom-caption" id="figure-2-desc"><p>Fusing metrics of cell heterogeneity increases the percentage of validated connections. <b>a</b> When median, MAD and random projections of covariance profiles are combined through SNF (red line), the enrichment in having same MOA/pathway annotations is improved, especially for the strongest, most relevant connections above 0.5%. This is shown in three separate experiments involving small molecules (left, right) and gene overexpression (middle). Enrichment is versus a null distribution, which is based on the remainder of the connections. <b>b</b> Similarity graphs for the mechanism of action (MOA) class Adrenergic receptor antagonists, using different types of profiles in CDRPBIO-BBBC036-Bray. This MOA was chosen because it showed the highest improvement upon combining different profiles. The goal is a qualitative view on how data fusion improves within-MOA connectivities. Each node represents a compound, and two nodes are connected if the similarity of their corresponding profiles is ranked among the top 5% most-similar pairs. Median, MAD, and random projections of covariance profiles seem to be complementary for this MOA, as they cover mostly non-overlapping compound connections. The overall connectivity of compounds in this MOA is improved once these profiles are combined through SNF. Graph layouts are the same across data types and are based on the similarities in median + MAD + cov. (SNF); note that this causes the left-most graph to appear less cluttered and less connected, but the main purpose of the visualization is to observe the structure of connections, not the number of connections (which is quantified systematically in part <b>a</b>). <b>c</b> Weighted similarity graph as in the previous plot except that edge thicknesses are based on an exponential weighting of the ranked similarity values. Sub-clusters that are moderately present in two or three profile types (such as the one marked in red in bottom left) became stronger after applying data fusion using SNF</p></div></div><div class="u-text-right u-hide-print"><a class="c-article__pill-button" data-test="article-link" data-track="click" data-track-label="button" data-track-action="view figure" href="/articles/s41467-019-10154-8/figures/2" data-track-dest="link:Figure2 Full size image" aria-label="Full size image figure 2" rel="nofollow"><span>Full size image</span><svg width="16" height="16" focusable="false" role="img" aria-hidden="true" class="u-icon"><use xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#icon-eds-i-chevron-right-small"></use></svg></a></div></figure></div><p>The improvements are observed even when MOAs/pathways with few (fewer than five) compound/gene pairs are removed, confirming that the improvement was not driven by a few outlier groups. We also evaluated another method that implicitly accounts for heterogeneity (Factor Analysis on single-cell data<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e543">7</a></sup>), which performed poorer than the proposed method (but had been the best performing in a previously published, smaller dataset in a different application<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e547">7</a></sup>), as well as methods that do not account for heterogeneity (Supplementary Fig. <a data-track="click" data-track-label="link" data-track-action="supplementary material anchor" href="/articles/s41467-019-10154-8#MOESM1">1</a>). The improved intra-MOA similarities, especially in certain MOAs (Fig. <a data-track="click" data-track-label="link" data-track-action="figure anchor" href="/articles/s41467-019-10154-8#Fig2">2b, c</a>, Supplementary Tables <a data-track="click" data-track-label="link" data-track-action="supplementary material anchor" href="/articles/s41467-019-10154-8#MOESM1">3</a>–<a data-track="click" data-track-label="link" data-track-action="supplementary material anchor" href="/articles/s41467-019-10154-8#MOESM1">5</a>), indicates that median, MAD, and sparse projections of covariances are complementary sources of information.</p><p>The improvement in enrichment of top-correlated perturbation pairs is observed across the three datasets, which involve different experimental conditions and perturbation/annotation types. Although trivial concatenation of dispersion measures with the median profile has shown marginal improvement in the past<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e567">7</a></sup>, combining MAD and covariance with medians via data fusion provides consistent and substantial improvement (typically around 20%) in the mentioned enrichment score.</p><p>We conclude that capturing cell-to-cell heterogeneity is of value in image-based profiling of cell populations. Mean-averaged metrics from deep learning-based feature extractors have shown promise in image-based profiling; these metrics would likely also be improved by the method presented here. These and other strategies can now be tested and the results shared, because we provide the datasets publicly. Source code, image processing pipelines, and gene/compound annotation data to reproduce these results are available (<a href="https://github.com/carpenterlab/2018_rohban_natcomm">https://github.com/carpenterlab/2018_rohban_natcomm</a>).</p></div></div></section><section data-title="Methods"><div class="c-article-section" id="Sec4-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="Sec4">Methods</h2><div class="c-article-section__content" id="Sec4-content"><h3 class="c-article__sub-heading" id="Sec5">Annotations</h3><p>We used the Repurposing hub<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 16" title="Corsello, S. M. et al. The Drug Repurposing Hub: a next-generation drug library and information resource. Nat. Med. 23, 405–408 (2017)." href="/articles/s41467-019-10154-8#ref-CR16" id="ref-link-section-d52554175e595">16</a></sup>, <a href="https://clue.io/repurposing-app">https://clue.io/repurposing-app</a>, to annotate compounds with their mechanism of action (accessed on 28 February 2018). For missing annotations, we used other resources such as <a href="https://www.drugbank.ca">https://www.drugbank.ca</a>. The gene overexpression dataset contains biological pathway annotations, generated by domain experts at our institution. For pathways marked as having canonical and non-canonical members, we merged all members.</p><h3 class="c-article__sub-heading" id="Sec6">Rationale</h3><p>The theoretical basis we present assumes that the cellular phenotypes can be modelled as a mixture of gaussians. This model has been shown to be effective in capturing subpopulations in imaging data<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 8" title="Loo, L.-H. et al. An approach for extensibly profiling the molecular states of cellular subpopulations. Nat. Methods 6, 759–765 (2009)." href="/articles/s41467-019-10154-8#ref-CR8" id="ref-link-section-d52554175e621">8</a>,<a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 17" title="Slack, M. D., Martinez, E. D., Wu, L. F. &amp; Altschuler, S. J. Characterizing heterogeneous cellular responses to perturbations. Proc. Natl Acad. Sci. USA 105, 19306–19311 (2008)." href="/articles/s41467-019-10154-8#ref-CR17" id="ref-link-section-d52554175e624">17</a></sup>. In this model, the subpopulations and their proportions correspond to mixture centers and mixture prior probabilities, respectively. Both of these quantities are considered as unknown parameters.</p><p>It has been shown that, under mild assumptions, these unknown parameters can be estimated using the first, second, and third moments of data<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 11" title="Hsu, D. &amp; Kakade, S. M. Learning Mixtures of Spherical Gaussians: Moment Methods and Spectral Decompositions. In Proc. 4th Conference on Innovations in Theoretical Computer Science 11–20 (ACM, Berkeley, CA, USA 2013)." href="/articles/s41467-019-10154-8#ref-CR11" id="ref-link-section-d52554175e631">11</a></sup>. More specifically, if the mixtures are spherical Gaussians, and their centers are linearly independent, all the unknown parameters can be estimated with high precision given a sufficiently large number of data points (see Theorems 2 and 3<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 11" title="Hsu, D. &amp; Kakade, S. M. Learning Mixtures of Spherical Gaussians: Moment Methods and Spectral Decompositions. In Proc. 4th Conference on Innovations in Theoretical Computer Science 11–20 (ACM, Berkeley, CA, USA 2013)." href="/articles/s41467-019-10154-8#ref-CR11" id="ref-link-section-d52554175e635">11</a></sup>). In other words, the first, second, and third moments of the data constitute an approximate sufficient statistic for the unknown parameters in GMM when the sample size is sufficiently large. Average profiling uses only a small portion of this sufficient statistic–the first moment–to represent the sample. We can make this representation richer by also including the second and third moment profiles. Going beyond the third moment does not add any additional information with regard to the GMM (Theorems 2 and 3<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 11" title="Hsu, D. &amp; Kakade, S. M. Learning Mixtures of Spherical Gaussians: Moment Methods and Spectral Decompositions. In Proc. 4th Conference on Innovations in Theoretical Computer Science 11–20 (ACM, Berkeley, CA, USA 2013)." href="/articles/s41467-019-10154-8#ref-CR11" id="ref-link-section-d52554175e639">11</a></sup>).</p><p>We did not test the third moment because our datasets contain in the order of a few thousand cells per sample, whereas millions of cells would be needed to robustly compute third moments (O(d<sup>3</sup>), where d is the dimensionality of the feature space; on the order of 100 in our case). As well, the dimensionality of the final profiles rapidly grows as d increases. Although computing second-order moments is more feasible, it nonetheless requires dimensionality reduction to be of practical use: for 500 features, the second moment is nearly 125,000-dimensional, which is both computationally and statistically difficult to work with in forming the treatments similarity matrix. We use sparse random projections<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 12" title="Li, P., Hastie, T. J. &amp; Church, K. W. Very Sparse Random Projections. In Proc. 12th ACM SIGKDD International Conference on Knowledge Discovery and Data Mining 287–296 (ACM, Philadelphia, PA, USA 2006)." href="/articles/s41467-019-10154-8#ref-CR12" id="ref-link-section-d52554175e648">12</a></sup> of the vectorized covariance matrices to reduce the dimensionality to 3000 while approximately preserving pairwise profile distances.</p><h3 class="c-article__sub-heading" id="Sec7">Combining first and second-order moments</h3><p>Because the statistical distributions of mean, MAD, and covariance profiles can be different in general (Supplementary Fig. <a data-track="click" data-track-label="link" data-track-action="supplementary material anchor" href="/articles/s41467-019-10154-8#MOESM1">2</a>), we combined them at the sample similarities level, rather than simply concatenating the profiles. We use Similarity Network Fusion (SNF)<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 6" title="Wang, B. et al. Similarity network fusion for aggregating data types on a genomic scale. Nat. Methods 11, 333–337 (2014)." href="/articles/s41467-019-10154-8#ref-CR6" id="ref-link-section-d52554175e663">6</a></sup>, which operates on a graph representation of the dataset in each data type (in our case, three: medians, MADs, and covariances). A graph diffusion process is then used to combine the graph for each data type into the final network, which encodes the pairwise similarity values. SNF has shown great promise in fusing biological readouts when the number of samples is on the order of few hundreds<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 6" title="Wang, B. et al. Similarity network fusion for aggregating data types on a genomic scale. Nat. Methods 11, 333–337 (2014)." href="/articles/s41467-019-10154-8#ref-CR6" id="ref-link-section-d52554175e667">6</a></sup>. The method is expected to be less effective when sample size falls below a threshold as local neighbors start to become less similar, violating the assumptions made in the method<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 18" title="Wang, B., Jiang, J., Wang, W., Zhou, Z. H. &amp; Tu, Z. Unsupervised metric fusion by cross diffusion. In 2012 IEEE Conference on Computer Vision and Pattern Recognition 2997–3004 (IEEE, Providence, RI, USA 2012)." href="/articles/s41467-019-10154-8#ref-CR18" id="ref-link-section-d52554175e671">18</a></sup>. For this reason, we did not use the prior benchmark dataset in ref. <sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e675">7</a></sup>.</p><h3 class="c-article__sub-heading" id="Sec8">Parameter settings</h3><p>We used the SNFtool R package (Ver. 2.2.1) for data fusion to combine data types (median, MAD, and covariance profiles), and set the neighborhood size k = 7 in the similarity graph, gaussian weight function bandwidth μ = 0.5, and number of iterations T = 10 (for two data types) and T = 15 (for three data types) in SNF, which are typical choices for the algorithm. To avoid overfitting, we did not test alternative values of these parameters. Prior to applying SNF, similarity matrices are z-scored based on median and MAD and then linearly scaled to map 99.9th percentile to 0.999. This helps to make sure that the similarity values are on the same scale across data types.</p><p>We used 3000 sparse random projections with the density of <i>p</i> = 0.1 (the probability of an entry in the random projection matrix of being non-zero) to reduce the dimensionality of the covariance profiles in all the datasets. We observed reasonable consistency against randomness in the treatment correlation matrices when using around 3000 random projections (Supplementary Fig. <a data-track="click" data-track-label="link" data-track-action="supplementary material anchor" href="/articles/s41467-019-10154-8#MOESM1">3</a>). Pearson correlation of profiles is used to form similarity matrices, which are used as the inputs to SNF.</p><h3 class="c-article__sub-heading" id="Sec9">Factor analysis</h3><p>We performed exploratory factor analysis using factanal function in R and a model is trained on a random sample of 25,000 control cells of each dataset. Fifty factors were chosen, which accounted for ~76% of total variance. Factor score coefficients (loadings) were computed using regression and Varimax rotation of orthogonally uncorrelated factors. Loadings of standardized control cells were used to estimate factor scores.</p><h3 class="c-article__sub-heading" id="Sec10">Principal component analysis</h3><p>We performed principal component analysis using prcomp function in R (Ver. 3.3.3), and a model is trained on a random sample of 25,000 control cells of each dataset. Fifty principal components were chosen, which accounted for ~76% of total variance. Loadings of standardized control cells were used to compute principal component scores by multiplying it with the normalized data matrix.</p><h3 class="c-article__sub-heading" id="Sec11">Evaluation tasks</h3><p>We evaluated different profiling strategies in this paper (Fig. <a data-track="click" data-track-label="link" data-track-action="figure anchor" href="/articles/s41467-019-10154-8#Fig2">2</a>) based on whether the most-similar treatment pairs (above a given cutoff) are enriched for having the same MOA/pathway annotation, after removing un-annotated compounds. To ensure that strong profile similarities are not driven by systematic effects that might make samples on the same plate look more similar to each other than to those in other plates, all same-plate pairs were excluded in this analysis. To avoid introducing additional parameters, we did not filter for perturbations with strong phenotypes, although in practice, this could be a valuable step to further improve similarity predictions.</p><p>We rejected an alternative evaluation approach, accuracy in MOA/pathway classification<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e727">7</a></sup>, which only works well if MOAs are all well/equally represented in the dataset. The approach we took is better suited for the MOA class imbalance situation (as is the case for the datasets analyzed in this paper), as the enrichment is calculated based on a null distribution that tends to normalize MOA class sizes implicitly. Otherwise, treatments belonging to larger MOA classes tend to dominate the classification accuracy. Note that the chemical datasets we have presented reflect a huge variety of structures rather than a small number of compounds hand-picked to belong to particular classes; furthermore, annotations are sparse as many small molecules’ mechanisms are unknown. As a result, while the number of samples are large, they are spread across many classes, resulting in many classes with very few samples. Although alternate metrics such as F-score/precision/recall can help to mitigate class imbalances, they cannot overcome the small sizes for most classes in this dataset.</p><h3 class="c-article__sub-heading" id="Sec12">Enrichment score</h3><p>We define enrichment score as the odds ratio in a one-sided Fisher’s exact test, which tests whether having high profile similarity for a treatment pair is independent of the treatments sharing an MOA/pathway. To perform the test, we form the 2 × 2 contingency table by dividing treatment pairs into four categories, based on whether they have high profile correlations, determined by a specified threshold (in rows) and whether they share an MOA/pathway (in columns). The odds ratio is then defined as the ratio of elements in the first row divided by that of the second row in the contingency table. This roughly measures how likely it is to observe same MOA/pathway treatment pairs in highly correlated vs. non-highly correlated treatment pairs.</p></div></div></section> </div> <div> <section data-title="Data availability"><div class="c-article-section" id="data-availability-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="data-availability">Data availability</h2><div class="c-article-section__content" id="data-availability-content"> <p>We used three datasets to evaluate the profiling methods:</p> <p>CDRPBIO-BBBC036-Bray: 2200 known bioactive compounds in U2OS cells. This dataset is the bioactive subset of a publicly available dataset<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 15" title="Bray, M.-A. et al. A dataset of images and morphological profiles of 30 000 small-molecule treatments using the Cell Painting assay. Gigascience 6, 1–5 (2017)." href="/articles/s41467-019-10154-8#ref-CR15" id="ref-link-section-d52554175e806">15</a></sup>. Raw images are available at <a href="https://idr.openmicroscopy.org/webclient/?show=screen-1251">https://idr.openmicroscopy.org/webclient/?show = screen-1251</a>.</p> <p>Bioactives-BBBC022-Gustafsdottir: 1600 known bioactive compounds in U2OS cells. This is the image set BBBC022v1<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 14" title="Gustafsdottir, S. M. et al. Multiplex cytological profiling assay to measure diverse cellular states. PLoS One 8, e80999 (2013)." href="/articles/s41467-019-10154-8#ref-CR14" id="ref-link-section-d52554175e820">14</a></sup>, available from the Broad Bioimage Benchmark Collection<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 7" title="Ljosa, V. et al. Comparison of methods for image-based profiling of cellular morphological responses to small-molecule treatment. J. Biomol. Screen. 18, 1321–1329 (2013)." href="/articles/s41467-019-10154-8#ref-CR7" id="ref-link-section-d52554175e824">7</a></sup>. Raw images are available at <a href="https://data.broadinstitute.org/bbbc/BBBC022">https://data.broadinstitute.org/bbbc/BBBC022</a> and <a href="https://idr.openmicroscopy.org/webclient/?show=screen-1952">https://idr.openmicroscopy.org/webclient/?show = screen-1952</a>. The compounds in this dataset have some overlap with CDRPBIO.</p> <p>TA-ORF-BBBC037-Rohban: ~200 genes in various signaling pathways are over-expressed in U2OS cells<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 19" title="Rohban, M. H. et al. Systematic morphological profiling of human gene and allele function via Cell Painting. elife 6, e24060 (2017). " href="/articles/s41467-019-10154-8#ref-CR19" id="ref-link-section-d52554175e845">19</a></sup>. Raw images are publicly available at <a href="https://idr.openmicroscopy.org/webclient/?show=screen-1751">https://idr.openmicroscopy.org/webclient/?show = screen-1751</a>.</p> <p>In all three datasets, around 1700 single-cell image-based readouts were obtained by running the Cell Painting assay<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 13" title="Bray, M.-A. et al. Cell Painting, a high-content image-based assay for morphological profiling using multiplexed fluorescent dyes. Nat. Protoc. 11, 1757–1774 (2016)." href="/articles/s41467-019-10154-8#ref-CR13" id="ref-link-section-d52554175e860">13</a></sup> and an image processing pipeline in CellProfiler<sup><a data-track="click" data-track-action="reference anchor" data-track-label="link" data-test="citation-ref" aria-label="Reference 20" title="Carpenter, A. E. et al. CellProfiler: image analysis software for identifying and quantifying cell phenotypes. Genome Biol. 7, R100 (2006)." href="/articles/s41467-019-10154-8#ref-CR20" id="ref-link-section-d52554175e864">20</a></sup> software. The features are z-scored platewise in all datasets based on the negative controls.</p> <p>Extracted image-based features are publicly available in the following s3 bucket s3://cellpainting-datasets under folders corresponding to the respective names of the datasets.</p> </div></div></section><section data-title="Code availability"><div class="c-article-section" id="code-availability-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="code-availability">Code availability</h2><div class="c-article-section__content" id="code-availability-content"> <p>Source code, image processing pipelines, and gene/compound annotation data to reproduce these results are available (<a href="https://github.com/carpenterlab/2018_rohban_submitted">https://github.com/carpenterlab/2018_rohban_natcomm</a>).</p> </div></div></section><div id="MagazineFulltextArticleBodySuffix"><section aria-labelledby="Bib1" data-title="References"><div class="c-article-section" id="Bib1-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="Bib1">References</h2><div class="c-article-section__content" id="Bib1-content"><div data-container-section="references"><ol class="c-article-references" data-track-component="outbound reference" data-track-context="references section"><li class="c-article-references__item js-c-reading-companion-references-item" data-counter="1."><p class="c-article-references__text" id="ref-CR1">Janes, K. 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Funding for this work was provided by the BroadNext10 initiative of the Broad Institute and the National Institute of General Medical Sciences of the National Institutes of Health R35 GM122547 (to AEC).</p></div></div></section><section aria-labelledby="author-information" data-title="Author information"><div class="c-article-section" id="author-information-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="author-information">Author information</h2><div class="c-article-section__content" id="author-information-content"><h3 class="c-article__sub-heading" id="affiliations">Authors and Affiliations</h3><ol class="c-article-author-affiliation__list"><li id="Aff1"><p class="c-article-author-affiliation__address">Imaging Platform, Broad Institute of MIT and Harvard, Cambridge, MA, 02142, USA</p><p class="c-article-author-affiliation__authors-list">Mohammad H. Rohban, Hamdah S. Abbasi, Shantanu Singh &amp; Anne E. Carpenter</p></li><li id="Aff2"><p class="c-article-author-affiliation__address">Computer Engineering Department, Sharif University of Technology, Tehran, 11155/1639, Iran</p><p class="c-article-author-affiliation__authors-list">Mohammad H. Rohban</p></li></ol><div class="u-js-hide u-hide-print" data-test="author-info"><span class="c-article__sub-heading">Authors</span><ol class="c-article-authors-search u-list-reset"><li id="auth-Mohammad_H_-Rohban-Aff1-Aff2"><span class="c-article-authors-search__title u-h3 js-search-name">Mohammad H. Rohban</span><div class="c-article-authors-search__list"><div class="c-article-authors-search__item c-article-authors-search__list-item--left"><a href="/search?author=Mohammad%20H.%20Rohban" class="c-article-button" data-track="click" data-track-action="author link - publication" data-track-label="link" rel="nofollow">View author publications</a></div><div class="c-article-authors-search__item c-article-authors-search__list-item--right"><p class="search-in-title-js c-article-authors-search__text">You can also search for this author in <span class="c-article-identifiers"><a class="c-article-identifiers__item" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=search&amp;term=Mohammad%20H.%20Rohban" data-track="click" data-track-action="author link - pubmed" data-track-label="link" rel="nofollow">PubMed</a><span class="u-hide"> </span><a class="c-article-identifiers__item" href="http://scholar.google.co.uk/scholar?as_q=&amp;num=10&amp;btnG=Search+Scholar&amp;as_epq=&amp;as_oq=&amp;as_eq=&amp;as_occt=any&amp;as_sauthors=%22Mohammad%20H.%20Rohban%22&amp;as_publication=&amp;as_ylo=&amp;as_yhi=&amp;as_allsubj=all&amp;hl=en" data-track="click" data-track-action="author link - scholar" data-track-label="link" rel="nofollow">Google Scholar</a></span></p></div></div></li><li id="auth-Hamdah_S_-Abbasi-Aff1"><span class="c-article-authors-search__title u-h3 js-search-name">Hamdah S. Abbasi</span><div class="c-article-authors-search__list"><div class="c-article-authors-search__item c-article-authors-search__list-item--left"><a href="/search?author=Hamdah%20S.%20Abbasi" class="c-article-button" data-track="click" data-track-action="author link - publication" data-track-label="link" rel="nofollow">View author publications</a></div><div class="c-article-authors-search__item c-article-authors-search__list-item--right"><p class="search-in-title-js c-article-authors-search__text">You can also search for this author in <span class="c-article-identifiers"><a class="c-article-identifiers__item" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=search&amp;term=Hamdah%20S.%20Abbasi" data-track="click" data-track-action="author link - pubmed" data-track-label="link" rel="nofollow">PubMed</a><span class="u-hide"> </span><a class="c-article-identifiers__item" href="http://scholar.google.co.uk/scholar?as_q=&amp;num=10&amp;btnG=Search+Scholar&amp;as_epq=&amp;as_oq=&amp;as_eq=&amp;as_occt=any&amp;as_sauthors=%22Hamdah%20S.%20Abbasi%22&amp;as_publication=&amp;as_ylo=&amp;as_yhi=&amp;as_allsubj=all&amp;hl=en" data-track="click" data-track-action="author link - scholar" data-track-label="link" rel="nofollow">Google Scholar</a></span></p></div></div></li><li id="auth-Shantanu-Singh-Aff1"><span class="c-article-authors-search__title u-h3 js-search-name">Shantanu Singh</span><div class="c-article-authors-search__list"><div class="c-article-authors-search__item c-article-authors-search__list-item--left"><a href="/search?author=Shantanu%20Singh" class="c-article-button" data-track="click" data-track-action="author link - publication" data-track-label="link" rel="nofollow">View author publications</a></div><div class="c-article-authors-search__item c-article-authors-search__list-item--right"><p class="search-in-title-js c-article-authors-search__text">You can also search for this author in <span class="c-article-identifiers"><a class="c-article-identifiers__item" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=search&amp;term=Shantanu%20Singh" data-track="click" data-track-action="author link - pubmed" data-track-label="link" rel="nofollow">PubMed</a><span class="u-hide"> </span><a class="c-article-identifiers__item" href="http://scholar.google.co.uk/scholar?as_q=&amp;num=10&amp;btnG=Search+Scholar&amp;as_epq=&amp;as_oq=&amp;as_eq=&amp;as_occt=any&amp;as_sauthors=%22Shantanu%20Singh%22&amp;as_publication=&amp;as_ylo=&amp;as_yhi=&amp;as_allsubj=all&amp;hl=en" data-track="click" data-track-action="author link - scholar" data-track-label="link" rel="nofollow">Google Scholar</a></span></p></div></div></li><li id="auth-Anne_E_-Carpenter-Aff1"><span class="c-article-authors-search__title u-h3 js-search-name">Anne E. Carpenter</span><div class="c-article-authors-search__list"><div class="c-article-authors-search__item c-article-authors-search__list-item--left"><a href="/search?author=Anne%20E.%20Carpenter" class="c-article-button" data-track="click" data-track-action="author link - publication" data-track-label="link" rel="nofollow">View author publications</a></div><div class="c-article-authors-search__item c-article-authors-search__list-item--right"><p class="search-in-title-js c-article-authors-search__text">You can also search for this author in <span class="c-article-identifiers"><a class="c-article-identifiers__item" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=search&amp;term=Anne%20E.%20Carpenter" data-track="click" data-track-action="author link - pubmed" data-track-label="link" rel="nofollow">PubMed</a><span class="u-hide"> </span><a class="c-article-identifiers__item" href="http://scholar.google.co.uk/scholar?as_q=&amp;num=10&amp;btnG=Search+Scholar&amp;as_epq=&amp;as_oq=&amp;as_eq=&amp;as_occt=any&amp;as_sauthors=%22Anne%20E.%20Carpenter%22&amp;as_publication=&amp;as_ylo=&amp;as_yhi=&amp;as_allsubj=all&amp;hl=en" data-track="click" data-track-action="author link - scholar" data-track-label="link" rel="nofollow">Google Scholar</a></span></p></div></div></li></ol></div><h3 class="c-article__sub-heading" id="contributions">Contributions</h3><p>M.H.R., H.S.A, S.S., and A.E.C. all contributed to drafting the manuscript. M.H.R. proposed the novel profiling method, gathered the ground truth annotation, and analyzed the data with inputs from the other coauthors. H.S.A. contributed to the data analysis and benchmarked some previously proposed profiling methods, including Factor Analysis and Principal Component Analysis. S.S. helped to make the datasets publicly available.</p><h3 class="c-article__sub-heading" id="corresponding-author">Corresponding author</h3><p id="corresponding-author-list">Correspondence to <a id="corresp-c1" href="mailto:rohban@sharif.edu">Mohammad H. Rohban</a>.</p></div></div></section><section data-title="Ethics declarations"><div class="c-article-section" id="ethics-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="ethics">Ethics declarations</h2><div class="c-article-section__content" id="ethics-content"> <h3 class="c-article__sub-heading" id="FPar1">Competing interests</h3> <p>The authors declare no competing interests.</p> </div></div></section><section data-title="Additional information"><div class="c-article-section" id="additional-information-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="additional-information">Additional information</h2><div class="c-article-section__content" id="additional-information-content"><p><b>Journal peer review information:</b> <i>Nature Communications</i> thanks the anonymous reviewer(s) for their contribution to the peer review of this work.</p><p><b>Publisher’s note:</b> Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p></div></div></section><section data-title="Supplementary information"><div class="c-article-section" id="Sec13-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="Sec13">Supplementary information</h2><div class="c-article-section__content" id="Sec13-content"><div data-test="supplementary-info"><div id="figshareContainer" class="c-article-figshare-container" data-test="figshare-container"></div><div class="c-article-supplementary__item" data-test="supp-item" id="MOESM1"><h3 class="c-article-supplementary__title u-h3"><a class="print-link" data-track="click" data-track-action="view supplementary info" data-test="supp-info-link" data-track-label="supplementary information" href="https://static-content.springer.com/esm/art%3A10.1038%2Fs41467-019-10154-8/MediaObjects/41467_2019_10154_MOESM1_ESM.pdf" data-supp-info-image="">Supplementary Information</a></h3></div></div></div></div></section><section data-title="Rights and permissions"><div class="c-article-section" id="rightslink-section"><h2 class="c-article-section__title js-section-title js-c-reading-companion-sections-item" id="rightslink">Rights and permissions</h2><div class="c-article-section__content" id="rightslink-content"> <p><b>Open Access</b> This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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id="citeas">Cite this article</h3><p class="c-bibliographic-information__citation">Rohban, M.H., Abbasi, H.S., Singh, S. <i>et al.</i> Capturing single-cell heterogeneity via data fusion improves image-based profiling. <i>Nat Commun</i> <b>10</b>, 2082 (2019). https://doi.org/10.1038/s41467-019-10154-8</p><p class="c-bibliographic-information__download-citation u-hide-print"><a data-test="citation-link" data-track="click" data-track-action="download article citation" data-track-label="link" data-track-external="" rel="nofollow" href="https://citation-needed.springer.com/v2/references/10.1038/s41467-019-10154-8?format=refman&amp;flavour=citation">Download citation<svg width="16" height="16" focusable="false" role="img" aria-hidden="true" class="u-icon"><use xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#icon-eds-i-download-medium"></use></svg></a></p><ul class="c-bibliographic-information__list" data-test="publication-history"><li 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