Author: QIAGEN Digital Insights
Author: qiagen
June 13, 2024

New QCI Interpret 2024 Release brings significant performance and scalability enhancements for high-throughput NGS

The latest QCI Interpret 2024 Release enhances performance of high-throughput NGS labs, improving turn-around time, diagnostic yield and quality of results

We are pleased to announce that a new release of our clinical decision support software, QIAGEN Clinical Insight Interpret (QCI Interpret), brings significant performance and scalability enhancements tailored for high-throughput, next-generation sequencing (NGS) labs. In the QCI Interpret 2024 Release, users will benefit from new features and improvements that enable seamless scale-up for faster turnaround times, enhanced process and test management, and greater user coordination and flexibility.

QCI Interpret 2024 Release highlights for oncology and hereditary applications

  • Boost variant assessment speed and efficiency with the new Bulk Change Tool in the Variant List page: The magic wand button in the Variant List page allows you to apply the same assessment action, whether computed or from prior user assessments, to multiple selected variants, which eliminates the need for individual variant-by-variant assessments. You have the flexibility to choose whether to retain or overwrite assessment notes when applying bulk changes. This significantly reduces clicks and accelerates the assessment process. 
  • Supercharge your somatic workflow with enhanced co-occurring variants alerting: QCI Interpret now alerts you early in the workflow (Variant List, Variant Details, and Review & Report pages) of co-occurring variants with therapeutic significance. Co-occurring badges appear on variant tiles and flags appear on drugs where there are conflicting responses (e.g., both sensitive and resistant) associated with the co-presence of different variants within the same case. QCI Interpret for Hereditary and QCI Interpret for Oncology reports now prominently highlight interactions, ensuring both you and the physician are immediately informed of co-occurring variants that may impact treatment recommendations. 
  • Seamless, automated subject identification and comparison of results from somatic tests: QCI Interpret now automatically identifies when a subject ID has been encountered previously. A new Compare tool on the Review & Report page allows you to select and compare the variants between the current test and another test associated with the same subject. This simplifies the process of comparing variants and variant allele fractions for subjects tested multiple times, providing you with an efficient and user-friendly workflow. 
  • New tools for user group coordination and communication: These enhancements empower you to tailor your test organization strategy, providing a more personalized and efficient workflow within the Test List UI. High-volume labs can streamline test prioritization by associating test tag(s) to specific tests through the API and by filtering tests by these tags in the Test List UI. Additionally, the application now presents you with indicators inside the test when concurrent users from the same group have the same test open. This improvement aims to facilitate seamless coordination, preventing unintended overlap and duplication of work. Furthermore, you can now assign Due Dates to tests to efficiently prioritize your work.  
  • Expanded ability to add a treatment to a somatic report: In the QCI Interpret 202r Release, you can now manually add gene-targeted drug label sensitive findings and QCI Interpret-curated resistance findings to the treatment table on the Variant Details page. The added treatments are displayed on the Variant Details page, Review & Report page, and on the final report. This implementation ensures that you have additional flexibility to customize the treatment information in QCI Interpret and to include additional relevant treatment findings, on top of the comprehensive treatment recommendations offered by QCI Interpret. 
  • New somatic reporting policy that applies user-saved pathogenicity for all indications: This new somatic reporting policy empowers you to apply user-set pathogenicity in a phenotype-agnostic manner. You will benefit from the reuse of pathogenicity and reportability from the most recent user-saved assessment for consistent, time-saving reporting decisions.


Video: Learn more about the QCI Interpret 2024 Release highlights

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