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Compliance Information Platform "Green Line"

In response to the growing interest in SDGs and compliance in the manufacturing industry.

The "Green Line" is a new module of Total Materia that includes hazard information on materials and substances, as well as LCA (Life Cycle Assessment) and BoM (Bill of Materials) evaluation tools. It focuses on the increasing importance of corporate compliance and environmental sustainability. The perspective of compliance is no longer something that only quality assurance personnel consider. By taking into account the sustainability of materials used in the early stages of product design, it reduces rework and enhances not only productivity but also safety. If issues are found with materials, alternative materials can be quickly identified to respond to the problem swiftly.

  • Other information systems

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QCI Interpret Transparency and Acceleration of Human Germ Cell Mutation Evaluation

Automated evaluation support for human germ cell mutations with high transparency; conducting extensive mutation assessments derived from WGS/WES using a high-quality knowledge base.

QIAGEN Clinical Insight (QCI) Interpret supports the rapid evaluation and scaling up of human germline variant assessments for clinical NGS testing institutions and hereditary disease research organizations. QCI Interpret utilizes various knowledge bases, including the QIAGEN Knowledge Base (QKB), which has been continuously updated through manual curation for approximately 25 years, and the global database of causative gene mutations for hereditary diseases, HGMD Professional. This underpins the high transparency of decision-making support capabilities of QCI Interpret. The vast insights and information included in QCI Interpret enable the evaluation and reporting of variants in accordance with international guidelines (such as ACMG/AMP), the presentation of supporting references, and the reduction of VUS (variants of uncertain significance). QCI Interpret simplifies, accelerates, and reduces the cost of the work that testing and research institutions undertake to derive clinical and diagnostic significance from variant information. **Features** - High transparency in variant evaluation supported by evidence - Evaluation in accordance with guidelines

  • Bioinformatics

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