(A) Pedigree of the reported family. Main known phenotypes are mapped to individuals. Samples marked by a red star were available for Exome Sequencing. Proband is indicated with an arrow. (B) Bar plot representing prioritization scores obtained with Phenolyzer for genes identified from Exome Sequencing. GLI2 can be effectively associated with the clinical phenotype.</p
BackgroundGenome-wide association studies (GWAS) of common diseases have had a tremendous impact on ...
Cardiovascular disease (CVD) is a threat to public health. It has been reported to be the leading ca...
analysis to predict the analytic sensitivity of WES using pathogenic variants identified on targete...
Review on GLI2 (GLI family zinc finger 2), with data on DNA, on the protein encoded, and where the g...
The diagnostic yield of exome and genome sequencing remains low (8-70%), due to incomplete knowledge...
The translation of "next-generation" sequencing directly to the clinic is still being assessed but h...
Next generation sequencing is transforming clinical medicine and genome research, providing a powerf...
Many new disease genes can be identified through high-throughput sequencing. Yet, variant interpreta...
Background: Pinpointing genes involved in inherited human diseases remains a great challenge in the ...
Exome sequencing has identified the causes of several Mendelian diseases, although it has rarely bee...
Next-generation sequencing has catapulted healthcare into a revolutionary genomics era. One such tec...
Genome-wide association studies (GWAS) have successfully described the roles of common genetic varia...
Recent developments in high-throughput sequence capture methods and next-generation sequencing techn...
Whole-exome sequencing has revolutionized the identification of genes with dominant disease-associat...
Background: Germline sequencing of individual genomes can detect alleles responsible for adverse dru...
BackgroundGenome-wide association studies (GWAS) of common diseases have had a tremendous impact on ...
Cardiovascular disease (CVD) is a threat to public health. It has been reported to be the leading ca...
analysis to predict the analytic sensitivity of WES using pathogenic variants identified on targete...
Review on GLI2 (GLI family zinc finger 2), with data on DNA, on the protein encoded, and where the g...
The diagnostic yield of exome and genome sequencing remains low (8-70%), due to incomplete knowledge...
The translation of "next-generation" sequencing directly to the clinic is still being assessed but h...
Next generation sequencing is transforming clinical medicine and genome research, providing a powerf...
Many new disease genes can be identified through high-throughput sequencing. Yet, variant interpreta...
Background: Pinpointing genes involved in inherited human diseases remains a great challenge in the ...
Exome sequencing has identified the causes of several Mendelian diseases, although it has rarely bee...
Next-generation sequencing has catapulted healthcare into a revolutionary genomics era. One such tec...
Genome-wide association studies (GWAS) have successfully described the roles of common genetic varia...
Recent developments in high-throughput sequence capture methods and next-generation sequencing techn...
Whole-exome sequencing has revolutionized the identification of genes with dominant disease-associat...
Background: Germline sequencing of individual genomes can detect alleles responsible for adverse dru...
BackgroundGenome-wide association studies (GWAS) of common diseases have had a tremendous impact on ...
Cardiovascular disease (CVD) is a threat to public health. It has been reported to be the leading ca...
analysis to predict the analytic sensitivity of WES using pathogenic variants identified on targete...