<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Dimassi S</submitter><journal>Applied &amp; translational genomics</journal><pagination>19-25</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4803767</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA.</pubmed_title><pmcid>PMC4803767</pmcid><pubmed_authors>Labalme A</pubmed_authors><pubmed_authors>Dimassi S</pubmed_authors><pubmed_authors>Simonet T</pubmed_authors><pubmed_authors>Boutry-Kryza N</pubmed_authors><pubmed_authors>de Bellescize J</pubmed_authors><pubmed_authors>Lamy R</pubmed_authors><pubmed_authors>Schaeffer L</pubmed_authors><pubmed_authors>Lesca G</pubmed_authors><pubmed_authors>Chatron N</pubmed_authors><pubmed_authors>Sanlaville D</pubmed_authors><pubmed_authors>Roucher-Boulez F</pubmed_authors><pubmed_authors>Saad A</pubmed_authors><pubmed_authors>Campan-Fournier A</pubmed_authors><pubmed_authors>Bardel C</pubmed_authors><pubmed_authors>Putoux A</pubmed_authors><pubmed_authors>Elsensohn MH</pubmed_authors><pubmed_authors>Roy P</pubmed_authors><pubmed_authors>Calender A</pubmed_authors><pubmed_authors>Mougou-Zerelli S</pubmed_authors><pubmed_authors>Ville D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA.</name><description/><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Dec</publication><modification>2025-05-29T21:25:36.908Z</modification><creation>2024-11-08T17:38:10.848Z</creation></dates><accession>S-EPMC4803767</accession><cross_references><pubmed>27054081</pubmed><doi>10.1016/j.atg.2015.10.001</doi></cross_references></HashMap>