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Publication : High-Spatial-Resolution Multi-Omics Sequencing via Deterministic Barcoding in Tissue.

First Author  Liu Y Year  2020
Journal  Cell Volume  183
Issue  6 Pages  1665-1681.e18
PubMed ID  33188776 Mgi Jnum  J:299738
Mgi Id  MGI:6490145 Doi  10.1016/j.cell.2020.10.026
Citation  Liu Y, et al. (2020) High-Spatial-Resolution Multi-Omics Sequencing via Deterministic Barcoding in Tissue. Cell 183(6):1665-1681.e18
abstractText  We present deterministic barcoding in tissue for spatial omics sequencing (DBiT-seq) for co-mapping of mRNAs and proteins in a formaldehyde-fixed tissue slide via next-generation sequencing (NGS). Parallel microfluidic channels were used to deliver DNA barcodes to the surface of a tissue slide, and crossflow of two sets of barcodes, A1-50 and B1-50, followed by ligation in situ, yielded a 2D mosaic of tissue pixels, each containing a unique full barcode AB. Application to mouse embryos revealed major tissue types in early organogenesis as well as fine features like microvasculature in a brain and pigmented epithelium in an eye field. Gene expression profiles in 10-mum pixels conformed into the clusters of single-cell transcriptomes, allowing for rapid identification of cell types and spatial distributions. DBiT-seq can be adopted by researchers with no experience in microfluidics and may find applications in a range of fields including developmental biology, cancer biology, neuroscience, and clinical pathology.
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