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

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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Bibliographic Details
Main Authors: Milica Krunic, Peter Venhuizen, Leonhard Müllauer, Bettina Kaserer, Arndt von Haeseler
Format: Article
Language:English
Published: MDPI AG 2019-02-01
Series:Journal of Personalized Medicine
Subjects:
personalized medicine
cancer
amplicon sequencing
variant finding
pipeline
Online Access:https://www.mdpi.com/2075-4426/9/1/10

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