Your browser doesn't support javascript.
loading
Utilization of Benchtop Next Generation Sequencing Platforms Ion Torrent PGM and MiSeq in Noninvasive Prenatal Testing for Chromosome 21 Trisomy and Testing of Impact of In Silico and Physical Size Selection on Its Analytical Performance.
Minarik, Gabriel; Repiska, Gabriela; Hyblova, Michaela; Nagyova, Emilia; Soltys, Katarina; Budis, Jaroslav; Duris, Frantisek; Sysak, Rastislav; Gerykova Bujalkova, Maria; Vlkova-Izrael, Barbora; Biro, Orsolya; Nagy, Balint; Szemes, Tomas.
Afiliação
  • Minarik G; Institute of Molecular Biomedicine, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovakia.
  • Repiska G; Department of Molecular Biology, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
  • Hyblova M; Geneton Ltd., Bratislava, Slovakia.
  • Nagyova E; Institute of Molecular Biomedicine, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovakia.
  • Soltys K; Department of Molecular Biology, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
  • Budis J; Department of Molecular Biology, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
  • Duris F; Department of Molecular Biology, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
  • Sysak R; Department of Computer Science, Faculty of Mathematics, Physics and Informatics, Comenius University in Bratislava, Bratislava, Slovakia.
  • Gerykova Bujalkova M; Department of Molecular Biology, Faculty of Natural Sciences, Comenius University in Bratislava, Bratislava, Slovakia.
  • Vlkova-Izrael B; Department of Computer Science, Faculty of Mathematics, Physics and Informatics, Comenius University in Bratislava, Bratislava, Slovakia.
  • Biro O; 1st Department of Gynaecology and Obstetrics, Faculty of Medicine, Comenius University in Bratislava, Bratislava, Slovakia.
  • Nagy B; Department of Clinical Genetics, Medirex Inc., Bratislava, Slovakia.
  • Szemes T; Outpatient Clinic for Medical Genetics, Nemocnicna Inc., Malacky, Slovakia.
PLoS One ; 10(12): e0144811, 2015.
Article em En | MEDLINE | ID: mdl-26669558
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Cromossomos Humanos Par 21 / Simulação por Computador / Síndrome de Down / Sequenciamento de Nucleotídeos em Larga Escala Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Cromossomos Humanos Par 21 / Simulação por Computador / Síndrome de Down / Sequenciamento de Nucleotídeos em Larga Escala Idioma: En Ano de publicação: 2015 Tipo de documento: Article