Drupal-Biblio17<style face="normal" font="default" size="100%">CSVS, a crowdsourcing database of the Spanish population genetic variability.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">HGVA: the Human Genome Variation Archive.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Reference genome assessment from a population scale perspective: an accurate profile of variability and noise.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The role of the interactome in the maintenance of deleterious variability in human populations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Diversification of the expanded teleost-specific toll-like receptor family in Atlantic cod, Gadus morhua.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">VARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutation screening of multiple genes in Spanish patients with autosomal recessive retinitis pigmentosa by targeted resequencing.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Gene set-based analysis of polymorphisms: finding pathways or biological processes associated to traits in genome-wide association studies.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Use of estimated evolutionary strength at the codon level improves the prediction of disease-related protein mutations in humans.</style>