Human Y-chromosome variation in the genome-sequencing era
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics,Molecular Biology
Link
http://www.nature.com/articles/nrg.2017.36.pdf
Reference138 articles.
1. Bachtrog, D. Y-Chromosome evolution: emerging insights into processes of Y-chromosome degeneration. Nat. Rev. Genet. 14, 113–124 (2013).
2. Repping, S. et al. High mutation rates have driven extensive structural polymorphism among human Y chromosomes. Nat. Genet. 38, 463–467 (2006).
3. Jobling, M. A. Copy number variation on the human Y chromosome. Cytogenet. Genome Res. 123, 253–262 (2008).
4. Poznik, G. D. et al. Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Nat. Genet. 48, 593–599 (2016). This is the largest sequence-based study of Y-chromosome variation to be carried out thus far, and includes SNPs, STRs, indels, multiple nucleotide polymorphisms and CNVs; the data, DNA and cell lines are publicly available.
5. Heyer, E., Chaix, R., Pavard, S. & Austerlitz, F. Sex-specific demographic behaviours that shape human genomic variation. Mol. Ecol. 21, 597–612 (2012).
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