Add to ORKGian on f C an en nical obstacle to GWAS on rare variants is the calling predicted additional loci to be uncovered by more Wen and Yeh BMC Genomics 2014, 15:87
nt centage of the disease heritability [1,2]. The search for diseases. Although substantial efforts ...
Whole genome duplications followed by differentiation of many gene duplicates in the ancestors of ra...
Contains fulltext : 200373.pdf (publisher's version ) (Open Access)BACKGROUND: Lar...
Meta-analysis of genome-wide association studies (GWASs) has led to the discoveries of many common v...
available at the end of the article association studies (GWASs) can help in understanding the geneti...
Abstract: Hundreds of genetic variants have been associated to common diseases through genome-wide a...
ne tu ide ct in, w method is performed by targeting particular candidate genes or by quantitative tr...
Genome-wide association studies (GWAS) are identifying novel genomic loci associated with various di...
M3-S: a genotype calling method incorporating information from samples with known genotypes Gengxin ...
Genotype imputation is a key step in the analysis of genome-wide association studies (GWAS) and geno...
are Rare): methods to facilitate the analysis of iants from massively publication identifying XRCC2 ...
Genome-wide association studies (GWAS) and next generation sequencing (NGS) studies are powerful hig...
genomic signature of is ti n l a er he g e threshold (P-value = 5 × 10 – 5 × 10). Larger association...
To detect fully penetrant rare recessive variants that could constitute Mendelian subentities of com...
Next generation sequencing has dramatically increased our ability to localize disease-causing varian...
nt centage of the disease heritability [1,2]. The search for diseases. Although substantial efforts ...
Whole genome duplications followed by differentiation of many gene duplicates in the ancestors of ra...
Contains fulltext : 200373.pdf (publisher's version ) (Open Access)BACKGROUND: Lar...
Meta-analysis of genome-wide association studies (GWASs) has led to the discoveries of many common v...
available at the end of the article association studies (GWASs) can help in understanding the geneti...
Abstract: Hundreds of genetic variants have been associated to common diseases through genome-wide a...
ne tu ide ct in, w method is performed by targeting particular candidate genes or by quantitative tr...
Genome-wide association studies (GWAS) are identifying novel genomic loci associated with various di...
M3-S: a genotype calling method incorporating information from samples with known genotypes Gengxin ...
Genotype imputation is a key step in the analysis of genome-wide association studies (GWAS) and geno...
are Rare): methods to facilitate the analysis of iants from massively publication identifying XRCC2 ...
Genome-wide association studies (GWAS) and next generation sequencing (NGS) studies are powerful hig...
genomic signature of is ti n l a er he g e threshold (P-value = 5 × 10 – 5 × 10). Larger association...
To detect fully penetrant rare recessive variants that could constitute Mendelian subentities of com...
Next generation sequencing has dramatically increased our ability to localize disease-causing varian...
nt centage of the disease heritability [1,2]. The search for diseases. Although substantial efforts ...
Whole genome duplications followed by differentiation of many gene duplicates in the ancestors of ra...
Contains fulltext : 200373.pdf (publisher's version ) (Open Access)BACKGROUND: Lar...