Light-Seq combines high resolution imaging with next generation sequencing of selected cell populations in fixed biological samples. Specifically, microscopically analyzed cells can be subjected to RNA expression profiling while keeping the sample intact for further assays, enabling cellular phenotypes and states to be assessed in the context of the original tissue.
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References
Moses, L. & Pachter, L. Museum of spatial transcriptomics. Nat. Methods 19, 534–546 (2022). This review surveys the spatial transcriptomics methods landscape.
Nakamura, S., Kawabata, H. & Fujimoto, K. Double duplex invasion of DNA induced by ultrafast photo-cross-linking using 3-cyanovinylcarbazole for antigene methods. Chem. Commun. 53, 7616–7619 (2017). This paper reports light-directed DNA labeling by the ultrafast photocrosslinking chemistry that we use for Light-Seq barcoding.
Singh-Gasson, S. et al. Maskless fabrication of light-directed oligonucleotide microarrays using a digital micromirror array. Nat. Biotechnol. 17, 974–978 (1999). This paper describes the use of a digital micromirror array for the maskless fabrication of an oligonucleotide microarray.
Gustincich, S., Feigenspan, A., Wu, D. K., Koopman, L. J. & Raviola, E. Control of dopamine release in the retina: a transgenic approach to neural networks. Neuron 18, 723–736 (1997). This paper describes the morphology and function of the rare dopaminergic amacrine cell subtype.
Moen, E. et al. Deep learning for cellular image analysis. Nat. Methods 16, 1233–1246 (2019). This review discusses the intersection between deep learning and cellular image analysis.
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This is a summary of: Kishi, J. Y. et al. Light-Seq: light-directed in situ barcoding of biomolecules in fixed cells and tissues for spatially indexed sequencing. Nat. Methods https://doi.org/10.1038/s41592-022-01604-1 (2022).
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Light-Seq: from microscopy to transcriptomics and back. Nat Methods 19, 1353–1354 (2022). https://doi.org/10.1038/s41592-022-01608-x
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DOI: https://doi.org/10.1038/s41592-022-01608-x