Whole Genome and Transcriptome Analysis for Leukemia Diagnostics

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The rationale behind automating the assay lies primarily in improving quality and enhancing productivity. Automation minimizes the bias that can be introduced during manual library preparation. Additionally, the system is flexible enough to adapt to evolving laboratory needs.

  • High-throughput workflow for processing up to 5,000 patients
  • Standardized workflows for whole genome and transcriptome sequencing
  • Reduced bias compared to manual sample preparation

Library preparation is a critical step in many Next Generation Sequencing (NGS) applications, especially for sequencing and analyzing clinical samples—an essential component of modern medical diagnostics.

By automating the NGS workflow—including on-deck incubations, plate shaking, stacking, and managing a large tip inventory—hands-on time is significantly reduced. The system can process up to 96 samples in a single run. Automated barcode verification ensures correct placement of reagents, plates, and tips.

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