Background: There is growing interest in the role of rare variants in the variation of complex traits due to increasing evidence that rare variants are associated with quantitative traits. However, association methods that are commonly used for mapping common variants are not effective to map rare variants. Besides, livestock populations have large half-sib families and the occurrence of rare variants may be confounded with family structure, which makes it difficult to disentangle their effects from family mean effects. We compared the power of methods that are commonly applied in human genetics to map rare variants in cattle using whole-genome sequence data and simulated phenotypes. We also studied the power of mapping rare variants using ...
<div><p>The role of rare genetic variation in the etiology of complex disease remains unclear. Howev...
Although next-generation DNA sequencing technologies have made rare variant association studies feas...
Copy number variants (CNV) are insertions or deletions of 1 kb or larger in a genome with variable n...
International audienceAbstractBackground There is growing interest in the role of rare variants in t...
<p>The availability of whole genome sequence data enables to better explore the genetic mechanisms u...
With dense genotyping, many choices exist for methods to detect quantitative trait loci (QTL) in liv...
BACKGROUND: Relationships between individuals and inbreeding coefficients are commonly used for bree...
There is increasing use of dense single nucleotide polymorphisms (SNPs) for whole-genome association...
The proportion of genetic variation in complex traits explained by rare variants is a key ques-tion ...
<div><p>The proportion of genetic variation in complex traits explained by rare variants is a key qu...
The proportion of genetic variation in complex traits explained by rare variants is a key question f...
BACKGROUND: Availability of whole-genome sequence data for a large number of cattle and efficient im...
Genomic prediction estimates breeding values by exploiting linkage disequilibrium (LD) between quant...
The role of rare genetic variation in the etiology of complex disease remains unclear. However, the ...
Additional file 6: Figure S6. Comparison of the variances explained by SNPs between EMMAX_AMAT, EMMA...
<div><p>The role of rare genetic variation in the etiology of complex disease remains unclear. Howev...
Although next-generation DNA sequencing technologies have made rare variant association studies feas...
Copy number variants (CNV) are insertions or deletions of 1 kb or larger in a genome with variable n...
International audienceAbstractBackground There is growing interest in the role of rare variants in t...
<p>The availability of whole genome sequence data enables to better explore the genetic mechanisms u...
With dense genotyping, many choices exist for methods to detect quantitative trait loci (QTL) in liv...
BACKGROUND: Relationships between individuals and inbreeding coefficients are commonly used for bree...
There is increasing use of dense single nucleotide polymorphisms (SNPs) for whole-genome association...
The proportion of genetic variation in complex traits explained by rare variants is a key ques-tion ...
<div><p>The proportion of genetic variation in complex traits explained by rare variants is a key qu...
The proportion of genetic variation in complex traits explained by rare variants is a key question f...
BACKGROUND: Availability of whole-genome sequence data for a large number of cattle and efficient im...
Genomic prediction estimates breeding values by exploiting linkage disequilibrium (LD) between quant...
The role of rare genetic variation in the etiology of complex disease remains unclear. However, the ...
Additional file 6: Figure S6. Comparison of the variances explained by SNPs between EMMAX_AMAT, EMMA...
<div><p>The role of rare genetic variation in the etiology of complex disease remains unclear. Howev...
Although next-generation DNA sequencing technologies have made rare variant association studies feas...
Copy number variants (CNV) are insertions or deletions of 1 kb or larger in a genome with variable n...