The 1000 Genomes Project (1000G) is one of the most popular whole genome sequencing datasets used in different genomics fields and has boosting our knowledge in medical and population genomics, among other fields. Recent studies have reported the presence of ghost mutation signals in the 1000G. Furthermore, studies have shown that these mutations can influence the outcomes of follow-up studies based on the genetic variation of 1000G, such as single nucleotide variants (SNV) imputation. While the overall effect of these ghost mutations can be considered negligible for common genetic variants in many populations, the potential bias remains unclear when studying low frequency genetic variants in the population. In this study, we analyze the ef...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
Abstract Background Large sample sets of whole genome sequencing with deep coverage are being genera...
Abstract Background The Cancer Genome Atlas (TCGA) is a comprehensive database that includes multi-l...
Copy number variation (CNV) is pervasive in the human genome and has been shown to contribute signif...
The 1000 Genomes Project aims to provide a deep characterization of human genome sequence variation ...
Simulation output and Genome-wide scan for nIBD variants in UK10K data as reported in: Identifying ...
<div><p>Analyses investigating low frequency variants have the potential for explaining additional g...
The study of segmental duplications (SDs) and copy-number variants (CNVs) is of great importance in ...
International audienceThe increasing access to high-throughput sequencing is certainly one of the ma...
Genetic studies have shifted to sequencing-based rare variants discovery after decades of success in...
The invention of next generation sequencing techniques (NGS) marked the coming of a new era in the d...
In this work we present a new whole genome sequencing dataset with samples gathered from the Spanis...
High-throughput sequencing is a powerful tool, but suffers biases and errors that must be accounted ...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
Abstract Background Large sample sets of whole genome sequencing with deep coverage are being genera...
Abstract Background The Cancer Genome Atlas (TCGA) is a comprehensive database that includes multi-l...
Copy number variation (CNV) is pervasive in the human genome and has been shown to contribute signif...
The 1000 Genomes Project aims to provide a deep characterization of human genome sequence variation ...
Simulation output and Genome-wide scan for nIBD variants in UK10K data as reported in: Identifying ...
<div><p>Analyses investigating low frequency variants have the potential for explaining additional g...
The study of segmental duplications (SDs) and copy-number variants (CNVs) is of great importance in ...
International audienceThe increasing access to high-throughput sequencing is certainly one of the ma...
Genetic studies have shifted to sequencing-based rare variants discovery after decades of success in...
The invention of next generation sequencing techniques (NGS) marked the coming of a new era in the d...
In this work we present a new whole genome sequencing dataset with samples gathered from the Spanis...
High-throughput sequencing is a powerful tool, but suffers biases and errors that must be accounted ...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
Abstract Background Large sample sets of whole genome sequencing with deep coverage are being genera...
Abstract Background The Cancer Genome Atlas (TCGA) is a comprehensive database that includes multi-l...