Genes2Me

CliSeq Interpreter

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
  • Cancer and rare variants identification
  • Detection of SNV, CNV, InDels, fusions and gene rearrangement
  • Tumor Mutation Burden (TMB), Microsatellite Instability (MSI), Homologous Recombination Deficiency (HRD) score
  • Genes2Me
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