Mosaic-PICASSO: accurate crosstalk removal for multiplex fluorescence imaging
Motivation Ultra-multiplexed fluorescence imaging has revolutionized our understanding of biological systems, enabling the simultaneous visualization and quantification of multiple targets within biological specimens. A recent breakthrough in this field is PICASSO, a mutual-information-based techniq...
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| Vydáno v: | Bioinformatics (Oxford, England) Ročník 40; číslo 1 |
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| Hlavní autoři: | , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
England
Oxford University Press
02.01.2024
Oxford Publishing Limited (England) |
| Témata: | |
| ISSN: | 1367-4811, 1367-4803, 1367-4811 |
| On-line přístup: | Získat plný text |
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| Shrnutí: | Motivation
Ultra-multiplexed fluorescence imaging has revolutionized our understanding of biological systems, enabling the simultaneous visualization and quantification of multiple targets within biological specimens. A recent breakthrough in this field is PICASSO, a mutual-information-based technique capable of demixing up to 15 fluorophores without their spectra, thereby significantly simplifying the application of ultra-multiplexed fluorescence imaging. However, this study has identified a limitation of mutual information (MI)-based techniques. They do not differentiate between spatial colocalization and spectral mixing. Consequently, MI-based demixing may incorrectly interpret spatially co-localized targets as non-colocalized, leading to overcorrection.
Results
We found that selecting regions within a multiplex image with low-spatial similarity for measuring spectroscopic mixing results in more accurate demixing. This method effectively minimizes overcorrections and promises to accelerate the broader adoption of ultra-multiplex imaging.
Availability and implementation
The codes are available at https://github.com/xing-lab-pitt/mosaic-picasso. |
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| Bibliografie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
| ISSN: | 1367-4811 1367-4803 1367-4811 |
| DOI: | 10.1093/bioinformatics/btad784 |