<p>Background: Whole-genome genotyping techniques like Genotyping-by-sequencing (GBS) are being used for genetic studies such as Genome-Wide Association (GWAS) and Genomewide Selection (GS), where different strategies for imputation have been developed. Nevertheless, imputation error may lead to poor performance (i.e. smaller power or higher false positive rate) when complete data is not required as it is for GWAS, and each marker is taken at a time. The aim of this study was to compare the performance of GWAS analysis for Quantitative Trait Loci (QTL) of major and minor effect using different imputation methods when no reference panel is available in a wheat GBS panel. Results: In this study, we compared the power and false positive rate o...
Imputation is an in silico method that can increase the power of association studies by inferring mi...
Background: Genome wide association studies (GWAS) are becoming the approach of choice to identify g...
Wheat GBS dataset with 25 % missing information. Genotypes are presented as rows and SNPs as columns...
Background: Whole-genome genotyping techniques like Genotyping-by-sequencing (GBS) are being used fo...
Genotyping-by-sequencing (GBS) provides high SNP coverage and has recently emerged as a popular tech...
Key message: Imputing genotypes from the 90K SNP chip to exome sequence in wheat was moderately accu...
Well-powered genomic studies require genome-wide marker coverage across many individuals. For non-mo...
Background Success in genome-wide association studies and marker-assisted selection depends on good ...
Power (PO) and false positives rate (FPR) with 25 QTL and 25 % missing rate, for major and minor QTL...
Genome-wide molecular markers are often being used to evaluate genetic diversity in germplasm collec...
<div><p>Missing data are an unavoidable component of modern statistical genetics. Different array or...
Background: Imputation of partially missing or unobserved genotypes is an indispensable tool for SNP...
Power (PO) and false positives rate (FPR) with 25 QTL, for major and minor QTL for ascertainment bia...
As the amount of data from genome wide association studies grows dramatically, many interesting scie...
As the amount of data from genome wide association studies grows dramatically, many interesting scie...
Imputation is an in silico method that can increase the power of association studies by inferring mi...
Background: Genome wide association studies (GWAS) are becoming the approach of choice to identify g...
Wheat GBS dataset with 25 % missing information. Genotypes are presented as rows and SNPs as columns...
Background: Whole-genome genotyping techniques like Genotyping-by-sequencing (GBS) are being used fo...
Genotyping-by-sequencing (GBS) provides high SNP coverage and has recently emerged as a popular tech...
Key message: Imputing genotypes from the 90K SNP chip to exome sequence in wheat was moderately accu...
Well-powered genomic studies require genome-wide marker coverage across many individuals. For non-mo...
Background Success in genome-wide association studies and marker-assisted selection depends on good ...
Power (PO) and false positives rate (FPR) with 25 QTL and 25 % missing rate, for major and minor QTL...
Genome-wide molecular markers are often being used to evaluate genetic diversity in germplasm collec...
<div><p>Missing data are an unavoidable component of modern statistical genetics. Different array or...
Background: Imputation of partially missing or unobserved genotypes is an indispensable tool for SNP...
Power (PO) and false positives rate (FPR) with 25 QTL, for major and minor QTL for ascertainment bia...
As the amount of data from genome wide association studies grows dramatically, many interesting scie...
As the amount of data from genome wide association studies grows dramatically, many interesting scie...
Imputation is an in silico method that can increase the power of association studies by inferring mi...
Background: Genome wide association studies (GWAS) are becoming the approach of choice to identify g...
Wheat GBS dataset with 25 % missing information. Genotypes are presented as rows and SNPs as columns...