The impact of erroneous genotypes having passed standard quality control (QC) can be severe in genome-wide association studies, genotype imputation, and estimation of heritability and prediction of genetic risk based on single nucleotide polymorphisms (SNP). To detect such genotyping errors, a simple two-locus QC method, based on the difference in test statistic of association between single SNPs and pairs of SNPs, was developed and applied. The proposed approach could detect many problematic SNPs with statistical significance even when standard single SNP QC analyses fail to detect them in real data. Depending on the data set used, the number of erroneous SNPs that were not filtered out by standard single SNP QC but detected by the propose...
Genome-wide association studies are now widely used tools to identify genes and/or regions which may...
We introduce a simple and yet scientifically objective criterion for identifying SNPs with genotypin...
Imputation is an extremely valuable tool in conducting and synthesising genome-wide association stud...
The impact of erroneous genotypes having passed standard quality control (QC) can be severe in genom...
The impact of erroneous genotypes having passed standard quality control (QC) can be severe in genom...
The impact of erroneous genotypes having passed standard quality control (QC) can be severe in genom...
Motivation: The quality control (QC) filtering of single nucleotide polymorphisms (SNPs) is an impor...
High density single nucleotide polymorphism (SNP) genotyping panels provide an alternative to micros...
Allele transmissions in pedigrees provide a natural way of evaluating the genotyping quality of a pa...
High-throughput genomic technologies offer powerful ways to identify genetic determinants of complex...
ABSTRACT Quality control filtering of single-nucleotide polymorphisms (SNPs) is a key step when anal...
<div><p>During the last several years, high-density genotyping SNP arrays have facilitated genome-wi...
Abstract Background One common goal of a case/control genome wide association study (GWAS) is to fin...
ABSTRACT.Quality control filtering of single nucleotide polymorphisms (SNP) is a key step when analy...
Imputation is an extremely valuable tool in conducting and synthesising genome-wide association stud...
Genome-wide association studies are now widely used tools to identify genes and/or regions which may...
We introduce a simple and yet scientifically objective criterion for identifying SNPs with genotypin...
Imputation is an extremely valuable tool in conducting and synthesising genome-wide association stud...
The impact of erroneous genotypes having passed standard quality control (QC) can be severe in genom...
The impact of erroneous genotypes having passed standard quality control (QC) can be severe in genom...
The impact of erroneous genotypes having passed standard quality control (QC) can be severe in genom...
Motivation: The quality control (QC) filtering of single nucleotide polymorphisms (SNPs) is an impor...
High density single nucleotide polymorphism (SNP) genotyping panels provide an alternative to micros...
Allele transmissions in pedigrees provide a natural way of evaluating the genotyping quality of a pa...
High-throughput genomic technologies offer powerful ways to identify genetic determinants of complex...
ABSTRACT Quality control filtering of single-nucleotide polymorphisms (SNPs) is a key step when anal...
<div><p>During the last several years, high-density genotyping SNP arrays have facilitated genome-wi...
Abstract Background One common goal of a case/control genome wide association study (GWAS) is to fin...
ABSTRACT.Quality control filtering of single nucleotide polymorphisms (SNP) is a key step when analy...
Imputation is an extremely valuable tool in conducting and synthesising genome-wide association stud...
Genome-wide association studies are now widely used tools to identify genes and/or regions which may...
We introduce a simple and yet scientifically objective criterion for identifying SNPs with genotypin...
Imputation is an extremely valuable tool in conducting and synthesising genome-wide association stud...