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Missing Values in Longitudinal Proteome Dynamics Studies: Making a Case for Data Multiple Imputation.
Yan, Yu; Sankar, Baradwaj Simha; Mirza, Bilal; Ng, Dominic C M; Pelletier, Alexander R; Huang, Sarah D; Wang, Wei; Watson, Karol; Wang, Ding; Ping, Peipei.
  • Yan Y; Departments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
  • Sankar BS; NHLBI Integrated Cardiovascular Data Science Training Program, UCLA, Los Angeles, California 90095, United States.
  • Mirza B; NIH BRIDGE2AI Center & NHLBI Integrated Cardiovascular Data Science Training Program, UCLA, Suite 1-609, MRL Building, 675 Charles E. Young Drive South, Los Angeles, California 90095, United States.
  • Ng DCM; Departments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
  • Pelletier AR; NIH BRIDGE2AI Center & NHLBI Integrated Cardiovascular Data Science Training Program, UCLA, Suite 1-609, MRL Building, 675 Charles E. Young Drive South, Los Angeles, California 90095, United States.
  • Huang SD; Departments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
  • Wang W; NHLBI Integrated Cardiovascular Data Science Training Program, UCLA, Los Angeles, California 90095, United States.
  • Watson K; Departments of Physiology and Medicine, University of California, Los Angeles (UCLA) School of Medicine, Los Angeles, California 90095, United States.
  • Wang D; NHLBI Integrated Cardiovascular Data Science Training Program, UCLA, Los Angeles, California 90095, United States.
  • Ping P; NIH BRIDGE2AI Center & NHLBI Integrated Cardiovascular Data Science Training Program, UCLA, Suite 1-609, MRL Building, 675 Charles E. Young Drive South, Los Angeles, California 90095, United States.
J Proteome Res ; 23(9): 4151-4162, 2024 Sep 06.
Article en En | MEDLINE | ID: mdl-39189460
ABSTRACT
Temporal proteomics data sets are often confounded by the challenges of missing values. These missing data points, in a time-series context, can lead to fluctuations in measurements or the omission of critical events, thus hindering the ability to fully comprehend the underlying biomedical processes. We introduce a Data Multiple Imputation (DMI) pipeline designed to address this challenge in temporal data set turnover rate quantifications, enabling robust downstream analysis to gain novel discoveries. To demonstrate its utility and generalizability, we applied this pipeline to two use cases a murine cardiac temporal proteomics data set and a human plasma temporal proteomics data set, both aimed at examining protein turnover rates. This DMI pipeline significantly enhanced the detection of protein turnover rate in both data sets, and furthermore, the imputed data sets captured new representation of proteins, leading to an augmented view of biological pathways, protein complex dynamics, as well as biomarker-disease associations. Importantly, DMI exhibited superior performance in benchmark data sets compared to single imputation methods (DSI). In summary, we have demonstrated that this DMI pipeline is effective at overcoming challenges introduced by missing values in temporal proteome dynamics studies.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteoma / Proteómica Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteoma / Proteómica Límite: Animals / Humans Idioma: En Año: 2024 Tipo del documento: Article