The first five years of single-cell cancer genomics and beyond.

Abstract:

:Single-cell sequencing (SCS) is a powerful new tool for investigating evolution and diversity in cancer and understanding the role of rare cells in tumor progression. These methods have begun to unravel key questions in cancer biology that have been difficult to address with bulk tumor measurements. Over the past five years, there has been extraordinary progress in technological developments and research applications, but these efforts represent only the tip of the iceberg. In the coming years, SCS will greatly improve our understanding of invasion, metastasis, and therapy resistance during cancer progression. These tools will also have direct translational applications in the clinic, in areas such as early detection, noninvasive monitoring, and guiding targeted therapy. In this perspective, I discuss the progress that has been made and the myriad of unexplored applications that still lie ahead in cancer research and medicine.

journal_name

Genome Res

journal_title

Genome research

authors

Navin NE

doi

10.1101/gr.191098.115

subject

Has Abstract

pub_date

2015-10-01 00:00:00

pages

1499-507

issue

10

eissn

1088-9051

issn

1549-5469

pii

gr.191098.115

journal_volume

25

pub_type

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