Difference between revisions of "NGS-DesignTools"
m (Text replace - "([= ])Haplotype reconstruction," to "$1Haplotype inference,") |
m (Text replace - "RNA-Seq Quantitation" to "RNA-Seq quantification") |
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{{Bioinformatics application | {{Bioinformatics application | ||
|sw summary=Tools to assist in designing deep sequencing experiments for haplotype reconstruction and structural variant breakpoint detection | |sw summary=Tools to assist in designing deep sequencing experiments for haplotype reconstruction and structural variant breakpoint detection | ||
| − | |bio domain=Structural variation,RNA-Seq | + | |bio domain=Structural variation,RNA-Seq quantification |
|bio method=Haplotype inference, Modelling and simulation, | |bio method=Haplotype inference, Modelling and simulation, | ||
}} | }} | ||
Latest revision as of 16:54, 2 December 2015
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Application data |
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| Biological application domain(s) | Structural variation, RNA-Seq quantification |
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| Principal bioinformatics method(s) | Haplotype inference, Modelling and simulation |
| Maintained? | Maybe |
Summary: Tools to assist in designing deep sequencing experiments for haplotype reconstruction and structural variant breakpoint detection
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Description
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