VARIFI—Web-Based Automatic Variant Identification, Filtering and Annotation of Amplicon Sequencing Data

Fast and affordable benchtop sequencers are becoming more important in improving personalized medical treatment. Still, distinguishing genetic variants between healthy and diseased individuals from sequencing errors remains a challenge. Here we present VARIFI, a pipeline for finding reliable genetic...

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Detalles Bibliográficos
Autores principales: Krunic, Milica, Venhuizen, Peter, Müllauer, Leonhard, Kaserer, Bettina, von Haeseler, Arndt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463100/
https://www.ncbi.nlm.nih.gov/pubmed/30717290
http://dx.doi.org/10.3390/jpm9010010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463100/
https://www.ncbi.nlm.nih.gov/pubmed/30717290
http://dx.doi.org/10.3390/jpm9010010

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