A metric and workflow for quality control in the analysis of heterogeneity in phenotypic profiles and screens

被引:9
|
作者
Gough, Albert [1 ,2 ]
Shun, Tong Ying [1 ]
Taylor, D. Lansing [1 ,2 ]
Schurdak, Mark [1 ,2 ]
机构
[1] Univ Pittsburgh, Drug Discovery Inst, 3501 Fifth Ave,BST3 10052, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Computat & Syst Biol, 3501 Fifth Ave, Pittsburgh, PA USA
关键词
Heterogeneity; Phenotypic profiling; High content screening; Systems biology; Drug discovery; KOLMOGOROV-SMIRNOV TEST; TUMOR HETEROGENEITY; CELL VARIABILITY; ORIGINS; BIOLOGY; ERA; MICROENVIRONMENT; ESTABLISHMENT; MICROSCOPY; DISCOVERY;
D O I
10.1016/j.ymeth.2015.10.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Heterogeneity is well recognized as a common property of cellular systems that impacts biomedical research and the development of therapeutics and diagnostics. Several studies have shown that analysis of heterogeneity: gives insight into mechanisms of action of perturbagens; can be used to predict optimal combination therapies; and can be applied to tumors where heterogeneity is believed to be associated with adaptation and resistance. Cytometry methods including high content screening (HCS), high throughput microscopy, flow cytometry, mass spec imaging and digital pathology capture cell level data for populations of cells. However it is often assumed that the population response is normally distributed and therefore that the average adequately describes the results. A deeper understanding of the results of the measurements and more effective comparison of perturbagen effects requires analysis that takes into account the distribution of the measurements, i.e. the heterogeneity. However, the reproducibility of heterogeneous data collected on different days, and in different plates/slides has not previously been evaluated. Here we show that conventional assay quality metrics alone are not adequate for quality control of the heterogeneity in the data. To address this need, we demonstrate the use of the KolmogorovSmirnov statistic as a metric for monitoring the reproducibility of heterogeneity in an SAR screen, describe a workflow for quality control in heterogeneity analysis. One major challenge in high throughput biology is the evaluation and interpretation of heterogeneity in thousands of samples, such as compounds in a cell-based screen. In this study we also demonstrate that three heterogeneity indices previously reported, capture the shapes of the distributions and provide a means to filter and browse big data sets of cellular distributions in order to compare and identify distributions of interest. These metrics and methods are presented as a workflow for analysis of heterogeneity in large scale biology projects. (C) 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license
引用
收藏
页码:12 / 26
页数:15
相关论文
共 39 条
  • [1] Workflow and Metrics for Image Quality Control in Large-Scale High-Content Screens
    Bray, Mark-Anthony
    Fraser, Adam N.
    Hasaka, Thomas P.
    Carpenter, Anne E.
    JOURNAL OF BIOMOLECULAR SCREENING, 2012, 17 (02) : 266 - 274
  • [2] Deducing the mechanism of action of compounds identified in phenotypic screens by integrating their multiparametric profiles with a reference genetic screen
    Sundaramurthy, Varadharajan
    Barsacchi, Rico
    Chernykh, Mikhail
    Stoeter, Martin
    Tomschke, Nadine
    Bickle, Marc
    Kalaidzidis, Yannis
    Zerial, Marino
    NATURE PROTOCOLS, 2014, 9 (02) : 474 - 490
  • [3] Genetic and immunohistochemical analysis of psoriasis in Tunisian families: genetic and phenotypic heterogeneity
    Bougacha, N.
    Ammar, R.
    Marrakchi, S.
    Turki, H.
    Smahi, A.
    Ayadi, H.
    JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2016, 30 : 58 - 58
  • [4] High-content image analysis to study phenotypic heterogeneity in endothelial cell monolayers
    Chesnais, Francois
    Hue, Jonas
    Roy, Errin
    Branco, Marco
    Stokes, Ruby
    Pellon, Aize
    Le Caillec, Juliette
    Elbahtety, Eyad
    Battilocchi, Matteo
    Danovi, Davide
    Veschini, Lorenzo
    JOURNAL OF CELL SCIENCE, 2022, 135 (02)
  • [5] Regional heterogeneity in gene expression profiles: a transcript analysis in human and rat heart
    Sharma, S
    Razeghi, P
    Shakir, A
    Keneson, BJ
    Clubbb, F
    Taegtmeyer, H
    CARDIOLOGY, 2003, 100 (02) : 73 - 79
  • [6] Automated screening in environmental arrays allows analysis of quantitative phenotypic profiles in Saccharomyces cerevisiae
    Warringer, J
    Blomberg, A
    YEAST, 2003, 20 (01) : 53 - 67
  • [7] mQC: A Heuristic Quality-Control Metric for High-Throughput Drug Combination Screening
    Chen, Lu
    Wilson, Kelli
    Goldlust, Ian
    Mott, Bryan T.
    Eastman, Richard
    Davis, Mindy I.
    Zhang, Xiaohu
    McKnight, Crystal
    Klumpp-Thomas, Carleen
    Shinn, Paul
    Simmons, John
    Gormally, Mike
    Michael, Sam
    Thomas, Craig J.
    Ferrer, Marc
    Guha, Rajarshi
    SCIENTIFIC REPORTS, 2016, 6
  • [8] Analysis of Single Circulating Tumor Cells in Renal Cell Carcinoma Reveals Phenotypic Heterogeneity and Genomic Alterations Related to Progression
    Cappelletti, Vera
    Verzoni, Elena
    Ratta, Raffaele
    Vismara, Marta
    Silvestri, Marco
    Montone, Rosanna
    Miodini, Patrizia
    Reduzzi, Carolina
    Claps, Melanie
    Sepe, Pierangela
    Daidone, Maria Grazia
    Procopio, Giuseppe
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (04)
  • [9] Use of textbook outcome as a quality metric in hepatopancreaticobiliary surgery: a systematic review and meta-analysis
    Dawood, Zaiba Shafik
    Khalil, Mujtaba
    Waqar, Usama
    Banani, Illiyun
    Alidina, Zayan
    Pawlik, Timothy M.
    JOURNAL OF GASTROINTESTINAL SURGERY, 2025, 29 (05)
  • [10] Analysis of ecological environment quality heterogeneity across different landform types in Myanmar and its driving forces
    Shi, Shuangfu
    Peng, Shuangyun
    Lin, Zhiqiang
    Zhu, Ziyi
    Ma, Dongling
    Yin, Yuanyuan
    Lu, Xiangmei
    Li, Ting
    Gong, Luping
    ECOLOGICAL INDICATORS, 2024, 168