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 Resjournal_title
Genome researchauthors
Navin NEdoi
10.1101/gr.191098.115subject
Has Abstractpub_date
2015-10-01 00:00:00pages
1499-507issue
10eissn
1088-9051issn
1549-5469pii
gr.191098.115journal_volume
25pub_type
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