CliSeq Interpreter

Overview

CliSeq Interpreter is a cloud based data analysis software developed by Genes2Me. The software uses automated pipelines for detection of somatic and germline mutations from the raw data generated from major second generation sequencing platforms. FASTQ/ VCF files can be used as input and the pipeline will generate a comprehensive CSM report. CliSeq is GUI driven and user friendly requiring minimum expertise to use. It is Linux based and uses a GPU derived hardware system which makes it faster than many of the CPU only options.

Key Features

  • CSM reporting according to ACMG & AMP guidelines
  • Analysis using updated databases and automated pipelines
  • Cloud based data storage on regional AWS servers
  • Annotated VCF with MAF, gene name, location etc
  • Clinically significant variants with associated diseases
  • FCancer and rare variants identification
  • FDetection of SNV, CNV, InDels, fusions and gene rearrangement
  • Tumor Mutation Burden (TMB), Microsatellite Instability (MSI), Homologous Recombination Deficiency (HRD) score

Process Workflow

NGS workflow

Resources

Product Brochure
User Manual
Report File

Product Enquiry Form

Other Products

Since its inception in 2016, Genes2me has been constantly striving towards setting a benchmark in the diagnostics space by introducing premium quality (Made in India) diagnostic kits which are CE-IVD, ISO-13485:2016, and ISO 9001:2015 certified, assuring our clients of unparalleled quality and compliance with international standards.

© 2025 Genes2me. All rights reserved.