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Exome sequencing of multiple-sclerosis patients and their unaffected first-degree relatives.

Sheila Garcia-RosaMaria Galli de AmorimRenan ValierisVanessa Daccach MarquesJulio Cesar Cetrulo LorenziVania Balardin TollerGuilherme Sciascia do OlivalWilson Araújo da Silva JúniorIsrael Tojal da SilvaAmilton Antunes BarreiraDiana Noronha NunesEmmanuel Dias-Neto
Published in: BMC research notes (2017)
This dataset comprises the full exome of 28 Brazilian subjects grouped in eight distinct families, consisting of four complete trios (mother-patient-father) plus another four complete trios with one added unaffected sibling. In total, we present the full exome data of eight patients diagnosed with recurrent remittent multiple sclerosis. Diagnoses were made by experienced neurologists and all enrolled patients had at least 5 years of follow up and specific MS treatment. Exomes were sequenced from leukocyte-derived DNA, after the capture of exons using biotinylated probes, in the Ion Proton platform. For each exome we generated an average of 66.1 million good quality mapped reads with an average length of ~ 160nt. On average, for 90% of the exome a vertical coverage above 20× was reached.
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