Evidence map›Paper›PMID 33098413›Full record

ArticleBioinformatics (Oxford, England)2021

RobNorm: model-based robust normalization method for labeled quantitative mass spectrometry proteomics data.

Meng Wang, Lihua Jiang, Ruiqi Jian, Joanne Y Chan, Qing Liu, Michael P Snyder, Hua Tang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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  5. Article
  6. Evaluation of normalization strategies for mass spectrometry-based multi-omics datasets.Metabolomics : Official journal of the Metabolomic Society · 2025
    Article
  7. Article
  8. Review
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Meng WangDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Lihua JiangDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Ruiqi JianDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Joanne Y ChanDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Qing LiuDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Michael P SnyderDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Hua TangDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.

Funding

Genetic Architecture of Complex Traits in Admixed PopulationsR01GM073059 · NIGMS · STANFORD UNIVERSITY · PI TANG, HUA · 2005 to 2016
$2.4M
Machine Learning for Decoding the Genetic Architecture of Complex Traits and Diseases Across PopulationsR35GM127063 · NIGMS · STANFORD UNIVERSITY · PI Hua Tang · 2018 to 2026
$2.2M
Genotype-Tissue-Protein: proteomic variation and quantitative trait loci (pQTL)U01HG007611 · NHGRI · STANFORD UNIVERSITY · PI SNYDER, MICHAEL P., TANG, HUA · 2014 to 2014
$1.7M
NHGRI NIH HHS U01 HG007611NIGMS NIH HHS R01 GM073059NIGMS NIH HHS R35 GM127063
6 · The paper itself

Abstract

motivationData normalization is an important step in processing proteomics data generated in mass spectrometry experiments, which aims to reduce sample-level variation and facilitate comparisons of samples. Previously published methods for normalization primarily depend on the assumption that the distribution of protein expression is similar across all samples. However, this assumption fails when the protein expression data is generated from heterogenous samples, such as from various tissue types. This led us to develop a novel data-driven method for improved normalization to correct the systematic bias meanwhile maintaining underlying biological heterogeneity.

resultsTo robustly correct the systematic bias, we used the density-power-weight method to down-weigh outliers and extended the one-dimensional robust fitting method described in the previous work to our structured data. We then constructed a robustness criterion and developed a new normalization algorithm, called RobNorm.In simulation studies and analysis of real data from the genotype-tissue expression project, we compared and evaluated the performance of RobNorm against other normalization methods. We found that the RobNorm approach exhibits the greatest reduction in systematic bias while maintaining across-tissue variation, especially for datasets from highly heterogeneous samples. AVAILABILITYAND IMPLEMENTATION: https://github.com/mwgrassgreen/RobNorm. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsProteomicsComputer SimulationMass SpectrometryResearch Design

Identifiers

PMID33098413
PMCPMC8098025

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.