Journal article
Rongqin Ke, Marco Mignardi, T. Hauling, M. Nilsson
Human Mutation, 2016
Human Mutation, 2016
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APA
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Ke, R., Mignardi, M., Hauling, T., & Nilsson, M. (2016). Fourth Generation of Next‐Generation Sequencing Technologies: Promise and Consequences. Human Mutation.
Chicago/Turabian
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Ke, Rongqin, Marco Mignardi, T. Hauling, and M. Nilsson. “Fourth Generation of Next‐Generation Sequencing Technologies: Promise and Consequences.” Human Mutation (2016).
MLA
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Ke, Rongqin, et al. “Fourth Generation of Next‐Generation Sequencing Technologies: Promise and Consequences.” Human Mutation, 2016.
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@article{rongqin2016a,
title = {Fourth Generation of Next‐Generation Sequencing Technologies: Promise and Consequences},
year = {2016},
journal = {Human Mutation},
author = {Ke, Rongqin and Mignardi, Marco and Hauling, T. and Nilsson, M.}
}
Abstract
In this review, we discuss the emergence of the fourth‐generation sequencing technologies that preserve the spatial coordinates of RNA and DNA sequences with up to subcellular resolution, thus enabling back mapping of sequencing reads to the original histological context. This information is used, for example, in two current large‐scale projects that aim to unravel the function of the brain. Also in cancer research, fourth‐generation sequencing has the potential to revolutionize the field. Cancer Research UK has named “Mapping the molecular and cellular tumor microenvironment in order to define new targets for therapy and prognosis” one of the grand challenges in tumor biology. We discuss the advantages of sequencing nucleic acids directly in fixed cells over traditional next‐generation sequencing (NGS) methods, the limitations and challenges that these new methods have to face to become broadly applicable, and the impact that the information generated by the combination of in situ sequencing and NGS methods will have in research and diagnostics.