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Human Y-chromosome variation in the genome-sequencing era

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posted on 2017-11-03, 15:43 authored by Mark A. Jobling, Chris Tyler-Smith
The properties of the human Y chromosome - namely, male specificity, haploidy and escape from crossing over - make it an unusual component of the genome, and have led to its genetic variation becoming a key part of studies of human evolution, population history, genealogy, forensics and male medical genetics. Next-generation sequencing (NGS) technologies have driven recent progress in these areas. In particular, NGS has yielded direct estimates of mutation rates, and an unbiased and calibrated molecular phylogeny that has unprecedented detail. Moreover, the availability of direct-to-consumer NGS services is fuelling a rise of 'citizen scientists', whose interest in resequencing their own Y chromosomes is generating a wealth of new data.

History

Citation

Nature Reviews Genetics, 2017, 18, pp. 485–497

Author affiliation

/Organisation/COLLEGE OF MEDICINE, BIOLOGICAL SCIENCES AND PSYCHOLOGY/MBSP Non-Medical Departments/Department of Genetics

Version

  • AM (Accepted Manuscript)

Published in

Nature Reviews Genetics

Publisher

Nature Reviews Genetics

issn

1471-0056

eissn

1471-0064

Copyright date

2017

Available date

2017-11-30

Publisher version

https://www.nature.com/nrg/journal/v18/n8/full/nrg.2017.36.html

Notes

The file associated with this record is under embargo until 6 months after publication, in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above.

Language

en

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