NGSanalyzer 1.0 – Identifying SNV and Indels from Short Read Sequence data

NGSanalyzer 1.0

:: DESCRIPTION

NGSanalyzer is a suit of tools for identifying SNV (single nucleotide variations) and indels (insertions and deletions) from short read sequence data.

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::DEVELOPER

Laboratory for Medical Science Mathematics

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 NGSanalyzer

:: MORE INFORMATION