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MagicViewer

NAR Web Server Collection entry number 10641

Description

MagicViewer allows easy visualization of short read mapping, and identification and annotation of genetic variation using next-generation sequencing data. Platforms covered include Roche 454, ABI SOLiD and Illumina.

Classification

Category: DNA
Subcategory: Annotations
Category: DNA
Subcategory: Mapping and Assembly
Category: DNA
Subcategory: Sequence Polymorphisms
Category: Human Genome
Subcategory: Annotations
Category: Human Genome
Subcategory: Sequence Polymorphisms

PubMed Abstract

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