Evidence map›Paper›PMID 33469060›Full record

ArticleScientific reports2021

A comparative study of evaluating missing value imputation methods in label-free proteomics.

Liang Jin, Yingtao Bi, Chenqi Hu, Jun Qu, Shichen Shen, Xue Wang, Yu Tian

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
16.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

92 citing papers in PubMed, 164 citations in OpenAlex.

  1. Preprocessing Large-Scale Proteomics Data.Methods in molecular biology (Clifton, N.J.) · 2027
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  14. TheJournal of fungi (Basel, Switzerland) · 2026
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  17. NAR genomics and bioinformatics · 2026
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32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Liang JinDrug Metabolism and Pharmacokinetics, AbbVie Bioresearch Center, Worcester, MA, 01605, USA.
Yingtao BiDiscovery and Exploratory Statistics, AbbVie Bioresearch Center, Worcester, MA, 01605, USA.
Chenqi HuDrug Metabolism and Pharmacokinetics, AbbVie Bioresearch Center, Worcester, MA, 01605, USA.
Jun QuDepartment of Pharmaceutical Science, SUNY at Buffalo, Buffalo, NY, 14228, USA.
Shichen ShenDepartment of Pharmaceutical Science, SUNY at Buffalo, Buffalo, NY, 14228, USA.
Xue WangDrug Metabolism and Pharmacokinetics, AbbVie Bioresearch Center, Worcester, MA, 01605, USA.
Yu TianDrug Metabolism and Pharmacokinetics, AbbVie Bioresearch Center, Worcester, MA, 01605, USA. yu.tian@abbvie.com.
AbbVie (United States) · USUniversity at Buffalo, State University of New York · US

Funding

University of Buffalo Clinical and Translational Science Institute - Supplement SchulyerUL1TR001412 · NCATS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MURPHY, TIMOTHY F · 2015 to 2024
$33.8M
NCATS NIH HHS UL1 TR001412
6 · The paper itself

Abstract

The presence of missing values (MVs) in label-free quantitative proteomics greatly reduces the completeness of data. Imputation has been widely utilized to handle MVs, and selection of the proper method is critical for the accuracy and reliability of imputation. Here we present a comparative study that evaluates the performance of seven popular imputation methods with a large-scale benchmark dataset and an immune cell dataset. Simulated MVs were incorporated into the complete part of each dataset with different combinations of MV rates and missing not at random (MNAR) rates. Normalized root mean square error (NRMSE) was applied to evaluate the accuracy of protein abundances and intergroup protein ratios after imputation. Detection of true positives (TPs) and false altered-protein discovery rate (FADR) between groups were also compared using the benchmark dataset. Furthermore, the accuracy of handling real MVs was assessed by comparing enriched pathways and signature genes of cell activation after imputing the immune cell dataset. We observed that the accuracy of imputation is primarily affected by the MNAR rate rather than the MV rate, and downstream analysis can be largely impacted by the selection of imputation methods. A random forest-based imputation method consistently outperformed other popular methods by achieving the lowest NRMSE, high amount of TPs with the average FADR < 5%, and the best detection of relevant pathways and signature genes, highlighting it as the most suitable method for label-free proteomics.

Indexed as

AlgorithmsData AnalysisDatasets as TopicElectronic Data ProcessingEscherichia coliEscherichia coli ProteinsHumansNeoplasm ProteinsProteomeProteomicsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsEscherichia coli ProteinsNeoplasm ProteinsProteomeSaccharomyces cerevisiae Proteins

Identifiers

PMID33469060
PMCPMC7815892
OpenAlexW3124839450

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.