NGS Analytical Toolkits 2017-05-19T14:34:00+00:00

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NGS Analytical Toolkits

A set of software modules that analyze a DNA sequence for variant mutations to produce a variant calling file. This VCF is then uploaded into the precision medicine platform workflow and compared with the information contained in the knowledge base to generate the patients individualized report. A complete set or individual modules are available for various types of analyses.

NGS Analytical Toolkits carry out analysis for:

  • Single nucleotide polymorphisms

  • Indels

  • Fusions

  • Copy number variations

  • Expressions

  • Epigenetics

  • CHIP-Seq

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