Rare missense variants within a single gene form yin yang haplotypes-Reference-Cited by-同舟云学术

Rare missense variants within a single gene form yin yang haplotypes

Published:2015-04-22 Issue:1 Volume:24 Page:139-141
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Curtis David

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg201574.pdf

Reference6 articles.

1. Zhang J, Rowe WL, Clark AG, Buetow KH : Genomewide distribution of high-frequency, completely mismatching SNP haplotype pairs observed to be common across human populations. Am J Hum Genet 2003; 73: 1073–1081.

2. Curtis D, Vine AE, Knight J : Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations. Ann Hum Genet 2008; 72: 261–278.

3. Curtis D, Vine AE : Yin yang haplotypes revisited - long, disparate haplotypes observed in European populations in regions of increased homozygosity. Hum Hered 2010; 69: 184–192.

4. Curtis D : Approaches to the detection of recessive effects using next generation sequencing data from outbred populations. Adv Appl Bioinform Chem 2013; 6: 29–35.

5. Abecasis GR, Auton A, Brooks LD et al: An integrated map of genetic variation from 1092 human genomes. Nature 2012; 491: 56–65.

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