QIAGEN Clinical Insight (QCI) Analyze for GeneReader
The bioinformatic complement to the GeneReader NGS System
QCI Analyze offers all the tools you need to guide your NGS data analysis together with the GeneRead QIAact targeted panel family on the GeneReader NGS System. QCI Analyze fully complements the GeneReader, from the setup of sequencing reactions to the automated analysis of sequencing results. The software includes optimized read alignment, variant calling, filtering and integrated visualization so your lab can confirm the analytic validity of your results. After reviewing your quality control (QC) reports and variant data in QCI Analyze, you can continue your interpretation of NGS variants in QCI Interpret.
QIAGEN Clinical Insight (QCI) Analyze is for Research Use Only. Not for use in diagnostic procedures
QCI Analyze is the last component of the GeneReader NGS System Sample to Insight solution, performing the secondary analysis of FASTQ reads generated by the GeneReader and providing a graphical interface to investigate detected variants. The software can also export the valid variants as VCF into QIAGEN Clinical Insight (QCI) Interpret.
QCI Analyze is a browser-based interface that uses the capabilities of the CLC Genomics Server and QIAGEN CLC bio algorithms to analyze Next Generation Sequencing (NGS) data. QCI Analyze can import NGS data, analyze it using a ready-to-use workflow, display results for inspection and if requested, connect directly to QCI Interpret.
QCI Analyze workflow
The QCI Analyze workflow provides streamlined and standardized analysis of the next-generation sequencing (NGS) data generated by the GeneReader. The workflow is automated, ensuring greater standardization and more accurate results. The QCI Analyze process includes:
The workflow creates a web accessible interactive report that includes:
Administrator options enable lab-specific criteria for variant reporting, thus locked down workflows for the general user.
QCI Analyze is a secondary analysis software intended for the analysis of data generated by automated sequencers like the GeneReader.
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