SNVer v.0.0.2



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Description

Detection of rare and common variants in next generation sequencing. SNVer call common and rare variants in the analysis of pool or individual next-generation sequencing data.
The software reports one single overall p-value for evaluating the significance of a candidate locus being a variant, based on which multiplicity control can be obtained.
Loci with any (low) coverage can be tested and depth of coverage will be quantitatively...
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  • Release Date:10/06/2012
  • License:Freeware
  • Category:Miscellaneous

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System Requirements

N/A

SNVer v.0.0.2 Copyright

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