Bioinformatics

Bioinformatics

Comprehensive bioinformatics solutions covering the entire genomic analysis workflow, from sequencing data processing to the clinical interpretation of genomic findings, tailored to the needs of research and diagnostic laboratories.

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Franklin™ by QIAGEN

One of the most advanced platforms for genomic sequencing data analysis and interpretation.

Franklin™ by QIAGEN is one of the most advanced platforms for the analysis and interpretation of genomic sequencing data. By leveraging artificial intelligence, clinical evidence, and publicly available databases, it provides automated, evidence-based variant interpretation. The platform can be fully customized to meet the specific needs of each laboratory and offers, among other features:

  • Secondary and tertiary analysis of sequencing data starting from FASTQ, BAM, and VCF files
  • Automated quality control (QC) and coverage report by genomic region or gene target
  • Analysis of copy number variants (CNVs), structural variants (SVs), and repeat expansions
  • Assessment of molecular biomarkers, including MSI, TMB, and LOH
  • Pharmacogenomic interpretation and links to approved targeted therapies
  • Support for internal knowledge bases and API integration to automate laboratory workflows

The platform helps reduce analysis turnaround time while improving the accuracy, consistency, and collaboration of genomic data interpretation across laboratory teams.

For more information, read our latest blog article or visit the Franklin™ by QIAGEN website.