TY - JOUR
T1 - Batch Effects in MALDI Mass Spectrometry Imaging
AU - Balluff, Benjamin
AU - Hopf, Carsten
AU - Siegel, Tiffany Porta
AU - Grabsch, Heike
AU - Heeren, Ron M. A.
N1 - Funding Information:
We thank Jian Hua Cao (M4i), Michele Genangeli (M4i), and Annika Kuhn (MUMC+) for providing the mass spectrometry imaging datasets. In this context, all patient data shown has been obtained with ethical approval and with patient consent. All animal data has been obtained in compliance with the EU regulations for animal experimentation. B.B., T.P.S., and R.M.A.H. are financially supported by the Dutch Province of Limburg as part of the LINK program. B.B. received financial support from the Dutch Cancer Foundation (KWF) and European Union (ERA-NET TRANSCAN 2; Grant No. 643638). C.H. received funding from the Klaus-Tschira-Foundation (Project MALDISTAR; grant 00.010.2019).
Publisher Copyright:
©
PY - 2021/3/3
Y1 - 2021/3/3
N2 - Mass spectrometry imaging (MSI) has become an indispensible tool for spatially resolved molecular investigation of tissues. One of the key application areas is biomedical research, where matrix-assisted laser desorption/ionization (MALDI) MSI is predominantly used due to its high-throughput capability, flexibility in the molecular class to investigate, and ability to achieve single cell spatial resolution. While many of the initial technical challenges have now been resolved, so-called batch effects, a phenomenon already known from other omics fields, appear to significantly impede reliable comparison of data from particular midsized studies typically performed in translational clinical research. This critical insight will discuss at what levels (pixel, section, slide, time, and location) batch effects can manifest themselves in MALDI-MSI data and what consequences this might have for biomarker discovery or multivariate classification. Finally, measures are presented that could be taken to recognize and/or minimize these potentially detrimental effects, and an outlook is provided on what is still needed to ultimately overcome these effects.
AB - Mass spectrometry imaging (MSI) has become an indispensible tool for spatially resolved molecular investigation of tissues. One of the key application areas is biomedical research, where matrix-assisted laser desorption/ionization (MALDI) MSI is predominantly used due to its high-throughput capability, flexibility in the molecular class to investigate, and ability to achieve single cell spatial resolution. While many of the initial technical challenges have now been resolved, so-called batch effects, a phenomenon already known from other omics fields, appear to significantly impede reliable comparison of data from particular midsized studies typically performed in translational clinical research. This critical insight will discuss at what levels (pixel, section, slide, time, and location) batch effects can manifest themselves in MALDI-MSI data and what consequences this might have for biomarker discovery or multivariate classification. Finally, measures are presented that could be taken to recognize and/or minimize these potentially detrimental effects, and an outlook is provided on what is still needed to ultimately overcome these effects.
KW - DIGESTION
KW - NORMALIZATION
KW - PROTEOMICS
KW - TISSUE
U2 - 10.1021/jasms.0c00393
DO - 10.1021/jasms.0c00393
M3 - Article
C2 - 33523675
SN - 1044-0305
VL - 32
SP - 628
EP - 635
JO - Journal of the American Society for Mass Spectrometry
JF - Journal of the American Society for Mass Spectrometry
IS - 3
ER -