{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T00:47:52Z","timestamp":1790729272114,"version":"4.1.0"},"reference-count":14,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2015,12,1]],"date-time":"2015-12-01T00:00:00Z","timestamp":1448928000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2015,7,18]],"date-time":"2015-07-18T00:00:00Z","timestamp":1437177600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Applied &amp; Translational Genomics"],"published-print":{"date-parts":[[2015,12]]},"DOI":"10.1016\/j.atg.2015.10.001","type":"journal-article","created":{"date-parts":[[2015,10,23]],"date-time":"2015-10-23T05:02:25Z","timestamp":1445576545000},"page":"19-25","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":30,"special_numbering":"C","title":["Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA"],"prefix":"10.1016","volume":"7","author":[{"given":"Sarra","family":"Dimassi","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas","family":"Simonet","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Audrey","family":"Labalme","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nadia","family":"Boutry-Kryza","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amandine","family":"Campan-Fournier","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Raphaelle","family":"Lamy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claire","family":"Bardel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mad-H\u00e9l\u00e9nie","family":"Elsensohn","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Florence","family":"Roucher-Boulez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nicolas","family":"Chatron","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Audrey","family":"Putoux","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Julitta","family":"de Bellescize","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Doroth\u00e9e","family":"Ville","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laurent","family":"Schaeffer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pascal","family":"Roy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Soumaya","family":"Mougou-Zerelli","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ali","family":"Saad","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alain","family":"Calender","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Damien","family":"Sanlaville","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gaetan","family":"Lesca","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.atg.2015.10.001_bb0005","doi-asserted-by":"crossref","first-page":"73","DOI":"10.7171\/jbt.13-2402-002","article-title":"Comparison of commercially available target enrichment methods for next-generation sequencing","volume":"24","author":"Bodi","year":"2013","journal-title":"J. Biomol. Tech."},{"key":"10.1016\/j.atg.2015.10.001_bb0010","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pcbi.1003031","article-title":"Shining a light on dark sequencing: characterising errors in Ion Torrent PGM data","volume":"9","author":"Bragg","year":"2013","journal-title":"PLoS Comput. Biol."},{"key":"10.1016\/j.atg.2015.10.001_bb0015","doi-asserted-by":"crossref","first-page":"354","DOI":"10.1038\/ejhg.2014.92","article-title":"Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform","volume":"23","author":"Della Mina","year":"2015","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.atg.2015.10.001_bb0020","article-title":"Whole-exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome","author":"Dimassi","year":"2015","journal-title":"Clin. Genet."},{"key":"10.1016\/j.atg.2015.10.001_bb0025","doi-asserted-by":"crossref","first-page":"576","DOI":"10.4065\/71.6.576","article-title":"Descriptive epidemiology of epilepsy: contributions of population-based studies from Rochester, Minnesota","volume":"71","author":"Hauser","year":"1996","journal-title":"Mayo Clin. Proc."},{"key":"10.1016\/j.atg.2015.10.001_bb0030","doi-asserted-by":"crossref","first-page":"1387","DOI":"10.1111\/j.1528-1167.2012.03516.x","article-title":"Targeted next generation sequencing as a diagnostic tool in epileptic disorders","volume":"53","author":"Lemke","year":"2012","journal-title":"Epilepsia"},{"key":"10.1016\/j.atg.2015.10.001_bb0035","doi-asserted-by":"crossref","first-page":"539","DOI":"10.1016\/j.neurol.2015.01.569","article-title":"Epilepsy genetics: the ongoing revolution","volume":"171","author":"Lesca","year":"2015","journal-title":"Rev. Neurol. (Paris)"},{"key":"10.1016\/j.atg.2015.10.001_bb0040","doi-asserted-by":"crossref","first-page":"1061","DOI":"10.1038\/ng.2726","article-title":"GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction","volume":"45","author":"Lesca","year":"2013","journal-title":"Nat. Genet."},{"key":"10.1016\/j.atg.2015.10.001_bb0045","doi-asserted-by":"crossref","first-page":"3200","DOI":"10.1093\/hmg\/ddu030","article-title":"Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis","volume":"23","author":"Martin","year":"2014","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.atg.2015.10.001_bb0050","doi-asserted-by":"crossref","first-page":"9331","DOI":"10.1038\/srep09331","article-title":"A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations","volume":"5","author":"Miya","year":"2015","journal-title":"Sci. Rep."},{"key":"10.1016\/j.atg.2015.10.001_bb0055","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1086\/316946","article-title":"CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy","volume":"68","author":"Phillips","year":"2001","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.atg.2015.10.001_bb0060","doi-asserted-by":"crossref","first-page":"535","DOI":"10.1038\/ejhg.2013.181","article-title":"Streamlined ion torrent PGM-based diagnostics: BRCA1 and BRCA2 genes as a model","volume":"22","author":"Tarabeux","year":"2014","journal-title":"Eur. J. Hum. Genet."},{"key":"10.1016\/j.atg.2015.10.001_bb0065","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1016\/j.ajhg.2014.06.006","article-title":"Mutations in SLC13A5 cause autosomal-recessive epileptic encephalopathy with seizure onset in the first days of life","volume":"95","author":"Thevenon","year":"2014","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.atg.2015.10.001_bb0070","doi-asserted-by":"crossref","first-page":"1927","DOI":"10.1016\/j.eplepsyres.2014.08.024","article-title":"A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in a Chinese patient with non-familial nocturnal frontal lobe epilepsy","volume":"108","author":"Wang","year":"2014","journal-title":"Epilepsy Res."}],"container-title":["Applied &amp; Translational Genomics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2212066115300351?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2212066115300351?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,8,31]],"date-time":"2019-08-31T17:04:02Z","timestamp":1567271042000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2212066115300351"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,12]]},"references-count":14,"alternative-id":["S2212066115300351"],"URL":"https:\/\/doi.org\/10.1016\/j.atg.2015.10.001","relation":{},"ISSN":["2212-0661"],"issn-type":[{"value":"2212-0661","type":"print"}],"subject":[],"published":{"date-parts":[[2015,12]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA","name":"articletitle","label":"Article Title"},{"value":"Applied & Translational Genomics","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.atg.2015.10.001","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2015 The Authors. Published by Elsevier B.V.","name":"copyright","label":"Copyright"}]}}