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A pre-processing pipeline to quantify, visualize, and reduce technical variation in protein microarray studies.
Bérubé, Sophie; Kobayashi, Tamaki; Wesolowski, Amy; Norris, Douglas E; Ruczinski, Ingo; Moss, William J; Louis, Thomas A.
Afiliación
  • Bérubé S; Department of Biostatistics, Johns Hopkins University Bloomberg, School of Public Health, Baltimore, MD, USA.
  • Kobayashi T; Department of Epidemiology, Johns Hopkins University Bloomberg, School of Public Health, Baltimore, MD, USA.
  • Wesolowski A; Department of Epidemiology, Johns Hopkins University Bloomberg, School of Public Health, Baltimore, MD, USA.
  • Norris DE; W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins University Bloomberg, School of Public Health, Baltimore, MD, USA.
  • Ruczinski I; Department of Biostatistics, Johns Hopkins University Bloomberg, School of Public Health, Baltimore, MD, USA.
  • Moss WJ; Department of Epidemiology, Johns Hopkins University Bloomberg, School of Public Health, Baltimore, MD, USA.
  • Louis TA; W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins University Bloomberg, School of Public Health, Baltimore, MD, USA.
Proteomics ; 22(3): e2100033, 2022 02.
Article en En | MEDLINE | ID: mdl-34668656
ABSTRACT
Technical variation, or variation from non-biological sources, is present in most laboratory assays. Correcting for this variation enables analysts to extract a biological signal that informs questions of interest. However, each assay has different sources and levels of technical variation, and the choice of correction methods can impact downstream analyses. Compared to similar assays such as DNA microarrays, relatively few methods have been developed and evaluated for protein microarrays, a versatile tool for measuring levels of various proteins in serum samples. Here, we propose a pre-processing pipeline to correct for some common sources of technical variation in protein microarrays. The pipeline builds upon an existing normalization method by using controls to reduce technical variation. We evaluate our method using data from two protein microarray studies and by simulation. We demonstrate that pre-processing choices impact the fluorescent-intensity based ranks of proteins, which in turn, impact downstream analysis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Perfilación de la Expresión Génica / Análisis por Matrices de Proteínas Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Perfilación de la Expresión Génica / Análisis por Matrices de Proteínas Idioma: En Año: 2022 Tipo del documento: Article