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Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases

BACKGROUND: Since the advent of next generation sequencing (NGS), several studies have tried to evaluate the relevance of targeted gene panel sequencing and whole exome sequencing for molecular diagnosis of mitochondrial diseases. The comparison between these different strategies is extremely diffic...

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Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: Plutino, Morgane, Chaussenot, Annabelle, Rouzier, Cécile, Ait-El-Mkadem, Samira, Fragaki, Konstantina, Paquis-Flucklinger, Véronique, Bannwarth, Sylvie
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5889585/
https://ncbi.nlm.nih.gov/pubmed/29625556
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0568-y
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