Analyze with Precision. Interpret with Confidence.
OVERCOMING THE BURGEONING BOTTLENECK
Helping you do more with less
As the rate and volume of raw NGS data generation increases, secondary analysis is becoming a significant bottleneck. The amount of computing power, storage space, security and regulatory compliance, and bioinformatics skill and resources required to keep secondary analysis on pace with sequencing demand is compounding. Today, the goal for many labs is to do more with less.
QCI Secondary Analysis
QCI Secondary Analysis is a new cloud-based service for NGS secondary analysis.
Scalable and workflow agnostic, QCI Secondary Analysis can be used with any NGS instrument and panel combination and seamlessly connects to QCI Interpret, QIAGEN’s platform for clinical NGS interpretation, to enable users to go from FASTQ to precision report through an integrated and automated workflow.
Why QCI Secondary Analysis
Unparalleled Efficiency
Reduce time and effort with a unified and streamlined workflow that lets you create, refine, validate, and execute pipelines with unprecedented speed.
Unlimited Growth
Scale your environment to meet demand for increased volume with exceptional uptime, powerful compute capacity, and minimal infrastructure investment.
Simple and Agnostic
Simplify set-up and onboarding with QCI Secondary Analysis, a panel- and workflow-agnostic service that can utilize data from any sequencer.
An integrated workflow from FASTQ to precision report
Panel- and workflow-agnostic, QCI Secondary Analysis can utilize data from any sequencer.
Raw FASTQ sequencing files can be directly uploaded to QCI Secondary Analysis. For labs using other sequencers, a bulk file uploader tool can be used to upload data to QCI Secondary Analysis.
Once data has been uploaded to QCI Secondary Analysis, users then select a pre-configured analysis pipeline that has been optimized for their lab’s specific panel, policies, and standard operating procedures (SOPs). Users also have the option to run and deploy any bioinformatics tools, such as QIAGEN’s CLC Genomics Workbench, within QCI Secondary Analysis.
QCI Secondary Analysis automates the analysis of multiple sequencing runs simultaneously, generating high-quality variant calls within minutes. Users can then visualize the analysis results, such as read pileups, in a genome browser directly from the cloud platform. Or, users can send VCF files directly to QCI Interpret, or download the results to send to the interpretation platform of their choice.
QCI Secondary Analysis seamlessly integrates with QCI Interpret, QIAGEN’s platform for NGS variant interpretation and reporting, via QCI Connect, a secure, cloud-based application. This enables users to go from FASTQ to a precision NGS report through an automated and streamlined workflow to further accelerate turnaround times.
Analyze an entire sequencing run in 5 simple steps
Highly flexible and efficient, QCI Secondary Analysis requires minimal resources and expertise to automate and rapidly analyzes an entire sequencing run with very limited hands-on time.
Upload raw sequencing data to QCI Secondary Analysis through a bulk uploader tool.
Select a pre-configured workflow optimized for your lab’s specific panel, policies, and SOPs.
Click “Start Analysis” and run sequencing data individually or in bulk. An email alert notifies you once the analysis is complete.
Visualize analysis results by sending BAM files directly to genome browsers accessible via the cloud-based platform.
Send VCF files directly to QCI Interpret for downstream interpretation and reporting. Or download the files to local storage and send to the interpretation platform of your choice through LIMS integration.
Request a free demo
Experience the power, flexibility, and simplicity of QCI Secondary Analysis for yourself. Schedule a free, personalized demonstration today.
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