Tracing single-cell histories

Lee, J. H. (February 2018) Tracing single-cell histories. Science, 359 (6375). pp. 521-522. ISSN 0036-8075

URL: https://www.ncbi.nlm.nih.gov/pubmed/29420280
DOI: 10.1126/science.aar6335

Abstract

DNA mutations accumulate at a steady pace across the human genome, passing from one generation to another. On the basis of the degree of shared mutations, a genealogical relationship can be reconstructed from ancient and modern individuals, allowing one to go back hundreds of thousands of years in human evolutionary history (1). Instead of comparing individuals, on pages 550 and 555 of this issue, Bae et al. (2) and Lodato et al. (3), respectively, assessed the rate of DNA mutation in single cells from developing and aging human brains, revealing mutational histories in neurodevelopment, aging, and neurodegeneration. These approaches also have implications for understanding complex diseases that could result from somatic mutations that arise later in life, such as cancer.

Item Type: Paper
Subjects: Investigative techniques and equipment > assays > Single cell sequencing
CSHL Authors:
Communities: CSHL labs > Lee lab
CSHL Cancer Center Program > Cancer Genetics
Depositing User: Matt Covey
Date: 2 February 2018
Date Deposited: 20 Feb 2018 20:43
Last Modified: 12 Jun 2018 16:16
PMCID: PMC5812680
Related URLs:
URI: http://repository.cshl.edu/id/eprint/36080

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