MagicViewer
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Application data |
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| Created by | Jinyu Wu |
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| Biological application domain(s) | Sequence assembly (de novo assembly), Exome capture, Genetic variation |
| Principal bioinformatics method(s) | Visualisation, SNP calling |
| Technology | Illumina |
| Created at | Institute of Genomic Medicine, Wenzhou Medical College, Wenzhou 325035, China |
| Maintained? | Yes |
| Input format(s) | FASTA, GFF, BAM |
| Programming language(s) | Java |
| Operating system(s) | platform-independent |
Summary: Large-scale short reads and sequencing depth visualization.
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As an integrated solution, MagicViewer can serve as a visualization tool to display large-scale reads, which featured with operating system-independence, user-friendly interface, multiple navigation, zoom mode and custom color schemes. Another predominate feature of MagicViewer is that it provides details of query options for users to identify, filter and annotate the genetic variation between large-scale short reads and reference genomes.
Holds great promise to easily visualize the short reads alignment, identify the genetic variation and associate them with the annotation information of reference genome.
Provides a user-friendly interface in which large-scale short reads and sequencing depth can be easily visualized in zoomable images under user definable color scheme through an operating system-independent manner with the implement of Java language. Meanwhile, it holds a versatile genetic variation annotation, filtration and visualization interface, providing details of query options, functional classifications, subset selection, sequence association and primer design.
Links
References
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