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Links tagged with 'indel mutation'

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inGAP-svTool Content

http://ingap.sourceforge.net

DNA > Sequence Polymorphisms

inGAP-sv is a web server to identify and visualize structural variation from paired end mapping data. Several important features including local depth of coverage, mapping quality and associated tandem repeats are used to evaluate the quality of the predicted structural variation.

NAR Web Server Issue 2011
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tagschromosome aberrations chromosome mapping computer simulation dna sequence analysis genetic variation high-throughput nucleotide sequencing indel mutation

MagicViewerTool Content

http://bioinformatics.zj.cn/magicviewer/

DNA > Annotations
DNA > Mapping and Assembly
DNA > Sequence Polymorphisms
Human Genome > Annotations
Human Genome > Sequence Polymorphisms

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.

NAR Web Server Issue 2010
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tagsgenetic variation genomics indel mutation sequence alignment sequence analysis single nucleotide polymorphism systems integration