| Literature DB >> 33188776 |
Yang Liu1, Mingyu Yang1, Yanxiang Deng1, Graham Su1, Archibald Enninful2, Cindy C Guo2, Toma Tebaldi3, Di Zhang2, Dongjoo Kim2, Zhiliang Bai2, Eileen Norris2, Alisia Pan2, Jiatong Li2, Yang Xiao2, Stephanie Halene3, Rong Fan4.
Abstract
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-μm 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.Entities:
Keywords: high spatial resolution; in situ barcoding; mouse embryo; next-generation sequencing; spatial multi-omics
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Year: 2020 PMID: 33188776 PMCID: PMC7736559 DOI: 10.1016/j.cell.2020.10.026
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582