proteiNorm - A User-Friendly Tool for Normalization and Analysis of TMT and Label-Free Protein Quantification.
Journal
ACS omega
ISSN: 2470-1343
Titre abrégé: ACS Omega
Pays: United States
ID NLM: 101691658
Informations de publication
Date de publication:
13 Oct 2020
13 Oct 2020
Historique:
received:
30
05
2020
accepted:
14
08
2020
entrez:
19
10
2020
pubmed:
20
10
2020
medline:
20
10
2020
Statut:
epublish
Résumé
The technological advances in mass spectrometry allow us to collect more comprehensive data with higher quality and increasing speed. With the rapidly increasing amount of data generated, the need for streamlining analyses becomes more apparent. Proteomics data is known to be often affected by systemic bias from unknown sources, and failing to adequately normalize the data can lead to erroneous conclusions. To allow researchers to easily evaluate and compare different normalization methods via a user-friendly interface, we have developed "proteiNorm". The current implementation of proteiNorm accommodates preliminary filters on peptide and sample levels followed by an evaluation of several popular normalization methods and visualization of the missing value. The user then selects an adequate normalization method and one of the several imputation methods used for the subsequent comparison of different differential expression methods and estimation of statistical power. The application of proteiNorm and interpretation of its results are demonstrated on two tandem mass tag multiplex (TMT6plex and TMT10plex) and one label-free spike-in mass spectrometry example data set. The three data sets reveal how the normalization methods perform differently on different experimental designs and the need for evaluation of normalization methods for each mass spectrometry experiment. With proteiNorm, we provide a user-friendly tool to identify an adequate normalization method and to select an appropriate method for differential expression analysis.
Identifiants
pubmed: 33073088
doi: 10.1021/acsomega.0c02564
pmc: PMC7557219
doi:
Types de publication
Journal Article
Langues
eng
Pagination
25625-25633Subventions
Organisme : NCRR NIH HHS
ID : M01 RR000080
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008792
Pays : United States
Déclaration de conflit d'intérêts
The authors declare no competing financial interest.
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