| Literature DB >> 31416630 |
Alexander A Boulgakov1, Andrew D Ellington1, Edward M Marcotte2.
Abstract
The spatial distribution of molecules and cells is fundamental to understanding biological systems. Traditionally, microscopies based on electromagnetic waves such as visible light have been used to localize cellular components by direct visualization. However, these techniques suffer from limitations of transmissibility and throughput. Complementary to optical approaches, biochemical techniques such as crosslinking can colocalize molecules without suffering the same limitations. However, biochemical approaches are often unable to combine individual colocalizations into a map across entire cells or tissues. Microscopy-by-sequencing techniques aim to biochemically colocalize DNA-barcoded molecules and, by tracking their thus unique identities, reconcile all colocalizations into a global spatial map. Here, we review this new field and discuss its enormous potential to answer a broad spectrum of questions.Entities:
Keywords: DNA microscopy; barcoding; localization; next-generation sequencing; oligonucleotides
Mesh:
Year: 2019 PMID: 31416630 PMCID: PMC6943198 DOI: 10.1016/j.tibtech.2019.06.001
Source DB: PubMed Journal: Trends Biotechnol ISSN: 0167-7799 Impact factor: 19.536