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Quantifying Colocalization by Correlation: The Pearson Correlation Coefficient is Superior to the Mander's Overlap Coefficient
Stockholms universitet, Naturvetenskapliga fakulteten, Wenner-Grens institut.
Stockholms universitet, Naturvetenskapliga fakulteten, Wenner-Grens institut.
2010 (engelsk)Inngår i: CYTOMETRY PART A, ISSN 1552-4922, Vol. 77A, nr 8, s. 733-742Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The Pearson correlation coefficient (PCC) and the Mander's overlap coefficient (MOC) are used to quantify the degree of colocalization between fluorophores. The MOC was introduced to overcome perceived problems with the PCC. The two coefficients are mathematically similar, differing in the use of either the absolute intensities (MOC) or of the deviation from the mean (PCC). A range of correlated datasets, which extend to the limits of the PCC, only evoked a limited response from the MOC. The PCC is unaffected by changes to the offset while the MOC increases when the offset is positive. Both coefficients are independent of gain. The MOC is a confusing hybrid measurement, that combines correlation with a heavily weighted form of co-occurrence, favors high intensity combinations, downplays combinations in which either or both intensities are low and ignores blank pixels. The PCC only measures correlation. A surprising finding was that the addition of a second uncorrelated population can substantially increase the measured correlation, demonstrating the importance of excluding background pixels. Overall, since the MOC is unresponsive to substantial changes in the data and is hard to interpret, it is neither an alternative to nor a useful substitute for the PCC. The MOC is not suitable for making measurements of colocalization either by correlation or co-occurrence.

sted, utgiver, år, opplag, sider
2010. Vol. 77A, nr 8, s. 733-742
Emneord [en]
correlation, colocalization, co-occurrence, Mander's overlap coefficient, Pearson correlation coefficient
Identifikatorer
URN: urn:nbn:se:su:diva-49195DOI: 10.1002/cyto.a.20896ISI: 000280432500005OAI: oai:DiVA.org:su-49195DiVA, id: diva2:377138
Merknad
authorCount :2Tilgjengelig fra: 2010-12-13 Laget: 2010-12-13 Sist oppdatert: 2022-02-24bibliografisk kontrollert

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