Analysis Software



NGeneAnalySysTM is an analysis software that analyzes the data produced by the NGS sequencing instrument and helps to report in clinical-grade.

By using more than 20 proven genetic information databases, it provides accurate and rapid genetic mutation information, and can be used efficiently for disease diagnosis through various data analysis.


NGeneAnalySysTM with

NGeneBio’s BRCAaccuTestTM dedicated analysis pipeline is installed and customized analytics pipeline can be built and utilized additionally.

Key Features

Analysis automation

From analysis request to result check in one operation

Perform automated pipelines that are robust against Job Scheduler based error protection


ACMG guideline

Compliance with ACMG guidelines for clinical use of NGS

Clinical application through biological analysis of genetic variation

Patient Information Interworking

Provides the function to perform integrated analysis by linking the genetic mutation information found with the patient’s clinical data


Provide QC report and  variant report

Provide clinical-grade mutation analysis report


Provide visualized data through a variety of charts

Database for clinical
application of genetic variation

Provide the highest level of genetic mutation information using more than 20 databases validated in six categories to provide clinical information on genetic variation

Use Optimal DB Categories
  • Classifies information into six categories to provide clinical information on genetic variation
  • Build 1 to 6 data bases per category
Database Features by Category
  • Problematic region (4 kinds) : Includes information on areas where sequencing errors occur frequently or where sequencing is difficult
  • Clinical DB (6 kinds) : Includes information on genetic diseases such as ClinVar, dbSNP, KOHBRA
  • Gene DB (3 kinds) : Provides integrative gene database including RefSeq and UCSC
  • Population DB (4 kinds) : Provides genetic variation by race, including Africa, Europe, and Asia
  • In Slico prediction (2 kinds) : Provides risk prediction database based on genetic variation
  • Variant Classifier (1 kind) : Provides clinical classification of genetic variation according to ACMG guidelines

Provide the highest level of genetic variation information using more than 20 data bases from 6 categories to provide clinical information on genetic variation