Comparison of human and mouse genomes has revealed that many non-coding regions have levels of sequence conservation similar to protein-coding genes. These regions have attracted a lot of attention as potentially functional genomic sequences. However, little is known about the effect mutations in these conserved non-coding regions have on fitness and how many of them are present in the human genome as deleterious polymorphisms. To gain insight into the selective constraints imposed on conserved non-coding and protein-coding regions, we compared substitution rates in primate and rodent lineages and analyzed the density and allele frequencies of human polymorphism. Genomic regions conserved between primate and rodent groups show higher relati...
We present an analysis of rates and patterns of microevolutionary phenomena that have shaped the hum...
PhDComparative genomic studies have identified noncoding regions of the genome which are often more ...
Contains fulltext : 71198.pdf (publisher's version ) (Open Access)Copy number vari...
Noncoding genetic variants are likely to influence human biology and disease, but recognizing functi...
There are many more selectively constrained noncoding than coding nucleotides in the mammalian genom...
Ultraconserved elements are stretches of consecutive nucleotides that are perfectly conserved in mul...
There are many more selectively constrained noncoding than coding nucleotides in the mammalian genom...
Abstract Background The strong linkage disequilibrium (LD) recently found in genic or exonic regions...
Understanding how genetic variation affects organism phenotype and fitness is a fundamental question...
Analysis of the human and mouse genomes identified an abundance of conserved non-genic sequences (CN...
Previous studies observed a higher ratio of divergences at nonsynonymous and synonymous sites (ω = d...
A comprehensive phylogenetic framework is indispensable for investigating the evolution of genomic f...
Although sequences containing regulatory elements located close to protein-coding genes are often on...
<div><p>The contribution of regulatory versus protein change to adaptive evolution has long been con...
Abstract Background Regions of the genome that are under evolutionary constraint across multiple spe...
We present an analysis of rates and patterns of microevolutionary phenomena that have shaped the hum...
PhDComparative genomic studies have identified noncoding regions of the genome which are often more ...
Contains fulltext : 71198.pdf (publisher's version ) (Open Access)Copy number vari...
Noncoding genetic variants are likely to influence human biology and disease, but recognizing functi...
There are many more selectively constrained noncoding than coding nucleotides in the mammalian genom...
Ultraconserved elements are stretches of consecutive nucleotides that are perfectly conserved in mul...
There are many more selectively constrained noncoding than coding nucleotides in the mammalian genom...
Abstract Background The strong linkage disequilibrium (LD) recently found in genic or exonic regions...
Understanding how genetic variation affects organism phenotype and fitness is a fundamental question...
Analysis of the human and mouse genomes identified an abundance of conserved non-genic sequences (CN...
Previous studies observed a higher ratio of divergences at nonsynonymous and synonymous sites (ω = d...
A comprehensive phylogenetic framework is indispensable for investigating the evolution of genomic f...
Although sequences containing regulatory elements located close to protein-coding genes are often on...
<div><p>The contribution of regulatory versus protein change to adaptive evolution has long been con...
Abstract Background Regions of the genome that are under evolutionary constraint across multiple spe...
We present an analysis of rates and patterns of microevolutionary phenomena that have shaped the hum...
PhDComparative genomic studies have identified noncoding regions of the genome which are often more ...
Contains fulltext : 71198.pdf (publisher's version ) (Open Access)Copy number vari...