VCF.Filter: interactive prioritization of disease-linked genetic variants from sequencing data

Next generation sequencing is widely used to link genetic variants to diseases, and it has massively accelerated the diagnosis and characterization of rare genetic diseases. After initial bioinformatic data processing, the interactive analysis of genome, exome, and panel sequencing data typically st...

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Detalles Bibliográficos
Publicado en:Nucleic Acids Res
Main Authors: Müller, Heiko, Jimenez-Heredia, Raul, Krolo, Ana, Hirschmugl, Tatjana, Dmytrus, Jasmin, Boztug, Kaan, Bock, Christoph
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2017
Assuntos:
Web Server Issue
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5570181/
https://ncbi.nlm.nih.gov/pubmed/28520890
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkx425
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