Over the past 15 years, sequencing of the human genome and The Cancer Genome Atlas (TCGA) project have led to comprehensive lists of single-nucleotide polymorphisms (SNPs) and gene mutations across a large number of human samples. However, our ability to predict the functional impact of SNPs and mutations on gene expression is still in its infancy. Here, we provide key examples to help understand how mutations present in genes can affect translational output
Summary Genome sequencing projects are discovering millions of genetic variants in humans, and inter...
Single nucleotide variations (SNVs) can result in loss or gain of protein functional sites. We analy...
International audienceBackground: A promising application of the huge amounts of genetic data curren...
Introduction: As a part of the Gene Regulators in Disease project (GRID), this study aims to create ...
Recent advances in high-throughput genome sequencing technology have paved the way for the field to ...
Recent advances in high-throughput genome sequencing technology have paved the way for the field to ...
Single-nucleotide polymorphisms (SNPs) are variations in the genome where one base pair can differ b...
Single-nucleotide polymorphisms (SNPs) are variations in the genome where one base pair can differ b...
International audienceBackground: A promising application of the huge amounts of genetic data curren...
Background: By definition, effect of synonymous single-nucleotide variants (SNVs) on protein folding...
Structural variants (SVs) rearrange large segments of DNA1 and can have profound consequences in evo...
BACKGROUND: Genome-wide association studies of common diseases for common, low penetrance causal var...
Upstream open reading frames (uORFs) are tissue-specific cis-regulators of protein translation. Isol...
International audienceBackground: A promising application of the huge amounts of genetic data curren...
International audienceBackground: A promising application of the huge amounts of genetic data curren...
Summary Genome sequencing projects are discovering millions of genetic variants in humans, and inter...
Single nucleotide variations (SNVs) can result in loss or gain of protein functional sites. We analy...
International audienceBackground: A promising application of the huge amounts of genetic data curren...
Introduction: As a part of the Gene Regulators in Disease project (GRID), this study aims to create ...
Recent advances in high-throughput genome sequencing technology have paved the way for the field to ...
Recent advances in high-throughput genome sequencing technology have paved the way for the field to ...
Single-nucleotide polymorphisms (SNPs) are variations in the genome where one base pair can differ b...
Single-nucleotide polymorphisms (SNPs) are variations in the genome where one base pair can differ b...
International audienceBackground: A promising application of the huge amounts of genetic data curren...
Background: By definition, effect of synonymous single-nucleotide variants (SNVs) on protein folding...
Structural variants (SVs) rearrange large segments of DNA1 and can have profound consequences in evo...
BACKGROUND: Genome-wide association studies of common diseases for common, low penetrance causal var...
Upstream open reading frames (uORFs) are tissue-specific cis-regulators of protein translation. Isol...
International audienceBackground: A promising application of the huge amounts of genetic data curren...
International audienceBackground: A promising application of the huge amounts of genetic data curren...
Summary Genome sequencing projects are discovering millions of genetic variants in humans, and inter...
Single nucleotide variations (SNVs) can result in loss or gain of protein functional sites. We analy...
International audienceBackground: A promising application of the huge amounts of genetic data curren...