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Daniel Gyllborg, Chika Yokota, Mats Nilsson 2019. In situ sequencing for RNA analysis in tissue sections. protocols.io https://dx.doi.org/10.17504/protocols.io.s8vehw6Copy Citation Copied
URL: https://dx.doi.org/DOI:10.17504/protocols.io.s8vehw6
Authors: Daniel Gyllborg, Chika Yokota, Mats Nilsson
Group: Human Cell Atlas Method Development Community, Molecular Diagnostics - Mats Nilsson Group, Neurodegeneration Method Development Community
Summary: In situ sequencing method for parallel targeted analysis of short RNA fragments in morphologically preserved tissue. This protocol can be used to detect RNA molecules at the single cell level to aid in the identification of cell types according to their gene expression. The technique uses padlock probes to target desired genes of interest and rolling circle amplification to amplify signal for a high throughput methodolgy of spatial transcriptomics. With the use of barcode sequencing, identification of numerous genes is possible through multiplexing.
Affiliations: Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden, Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden, Science for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden
External URL: https://www.nature.com/articles/nmeth.2563
Version: 1
Publication Date: 2019
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