scholarly journals Multiple linear combination (MLC) regression tests for common variants adapted to linkage disequilibrium structure

2016 ◽  
Vol 41 (2) ◽  
pp. 108-121 ◽  
Author(s):  
Yun Joo Yoo ◽  
Lei Sun ◽  
Julia G. Poirier ◽  
Andrew D. Paterson ◽  
Shelley B. Bull
2008 ◽  
Vol 53 (9) ◽  
pp. 850-856 ◽  
Author(s):  
Pornlada Nuchnoi ◽  
Jun Ohashi ◽  
Izumi Naka ◽  
Duangporn Nacapunchai ◽  
Katsushi Tokunaga ◽  
...  

2005 ◽  
Vol 33 (4) ◽  
pp. 582-585 ◽  
Author(s):  
J. Hardy ◽  
A. Pittman ◽  
A. Myers ◽  
K. Gwinn-Hardy ◽  
H.C. Fung ◽  
...  

The tau (MAPT) locus exists as two distinct clades, H1 and H2. The H1 clade has a normal linkage disequilibrium structure and is the only haplotype found in all populations except those derived from Caucasians. The H2 haplotype is the minor haplotype in Caucasian populations and is not found in other populations. It shows no recombination over a region of 2 Mb with the more common H1 haplotype. The distribution of the haplotype and analysis of the slippage of dinucleotide repeat markers within the haplotype suggest that it entered Homo sapiens populations between approx. 10000 and 30000 years ago. However, sequence comparison of the H2 haplotype with the H1 haplotype and with the chimp sequence suggests that the common founder of the H1 and H2 haplotypes was far earlier than this. We suggest that the H2 haplotype is derived from Homo neanderthalensis and entered H. sapiens populations during the co-existence of these species in Europe from approx. 45000 to 18000 years ago and that the H2 haplotype has been under selection pressure since that time, possibly because of the role of this H1 haplotype in neurodegenerative disease.


BMC Genomics ◽  
2015 ◽  
Vol 16 (1) ◽  
Author(s):  
Reuben J. Pengelly ◽  
William Tapper ◽  
Jane Gibson ◽  
Marcin Knut ◽  
Rick Tearle ◽  
...  

2019 ◽  
Author(s):  
Reginald D. Smith

AbstractThe allele frequency dependence of the ranges of all measures of linkage disequilibrium is well-known. The maximum values of commonly used parameters such as r2 and D vary depending on the allele frequencies at each locus. However, though this phenomenon is recognized and accounted for in many studies, the comprehensive mathematical framework underlying the limits of linkage disequilibrium measures at various frequency combinations is often heuristic or empirical. Here, it is demonstrated that underlying this behavior is the fundamental shift between linear and nonlinear dependence in the linkage disequilibrium structure between loci. The proportion of linear and nonlinear dependence can be estimated and it demonstrates how even the same values of r2 can have different implications for the nature of the overall dependence. One result of this is the value of D′, when defined as only a positive number, has a minimum value of |r|. Understanding this dependence is crucial to making correct inferences about the relationships between two loci in linkage disequilibrium.


2006 ◽  
Vol 11 (12) ◽  
pp. 1061-1061 ◽  
Author(s):  
D Harold ◽  
S Paracchini ◽  
T Scerri ◽  
M Dennis ◽  
N Cope ◽  
...  

2019 ◽  
Vol 15 ◽  
pp. P1306-P1307
Author(s):  
Alexander M. Kulminski ◽  
Leonardo Shu ◽  
Yury Loika ◽  
Liang He ◽  
Alireza Nazarian ◽  
...  

2005 ◽  
Vol 28 (3) ◽  
pp. 232-243 ◽  
Author(s):  
Nicola J. Camp ◽  
Jeff Swensen ◽  
Benjamin D. Horne ◽  
James M. Farnham ◽  
Alun Thomas ◽  
...  

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