Abstract
We developed a robust multiplex fluorescent in situ hybridization (FISH) technique in archival formalin-fixed, paraffin-embedded (FFPE) human tissue sections while preserving the microanatomical context. This identifies single-cell gene expression patterns by probing multiple, unique nascent RNA transcripts and yields predictive quantitative gene expression signatures.
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Acknowledgements
This work was supported in part by US National Institutes of Health CA-R33-083208 and by Aureon Laboratories.
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R.H.S. and C.C.-C. are scientific cofounders of Aureon Laboratories.
Supplementary information
Supplementary Table 1
Sequences used to generate probes. (PDF 46 kb)
Supplementary Table 2
Mean Number of Transcription Sites (with Standard Error of the Mean) per 100 Cells for each Diagnosis. (PDF 47 kb)
Supplementary Table 3
Diagnostic importance of gene expression profiling. (PDF 52 kb)
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Capodieci, P., Donovan, M., Buchinsky, H. et al. Gene expression profiling in single cells within tissue. Nat Methods 2, 663–665 (2005). https://doi.org/10.1038/nmeth786
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DOI: https://doi.org/10.1038/nmeth786
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