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%">267 Spanish exomes reveal population-specific differences in disease-related genetic variation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq).</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Assessing technical performance in differential gene expression experiments with external spike-in RNA control ratio mixtures.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Deciphering intrafamilial phenotypic variability by exome sequencing in a Bardet–Biedl family</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Deciphering intrafamilial phenotypic variability by exome sequencing in a Bardet-Biedl family.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">ngsCAT: a tool to assess the efficiency of targeted enrichment sequencing.</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%">Whole-exome sequencing identifies novel compound heterozygous mutations in USH2A in Spanish patients with autosomal recessive retinitis pigmentosa.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Initial genomics of the human nucleolus.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Modeling and managing experimental data using FuGE.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Statistical methods for analysis of high-throughput RNA interference screens</style>