QCI Interpret

JSON twin: https://www.healthaidb.com/software/qci-interpret.json

Company Name

QIAGEN Digital Insights

Product URL

https://www.qiagen.com/us/products/discovery-and-translational-research/next-generation-sequencing/informatics-and-data/interpretation-content-databases/qci-interpret/

Company URL

https://www.qiagen.com/us/

Categories

• clinical Decision Support
• health Data Analytics
• genomics
• Bioinformatics
• Genomic Data Analysis
• Variant Interpretation
• Clinical Reporting

Summary

QCI Interpret is a clinical decision support software by QIAGEN Digital Insights that enhances the interpretation and reporting of next-generation sequencing (NGS) data, improving turnaround times and diagnostic accuracy for high-throughput labs.

Description

QCI Interpret is a clinical decision support software developed by QIAGEN Digital Insights, designed to streamline the interpretation and reporting of next-generation sequencing (NGS) data. It leverages advanced artificial intelligence (AI) capabilities, including AI-derived literature searches and AI-trained phenotype-driven ranking, to accelerate critical lab performance criteria such as turnaround time, diagnostic yield, and result quality. The software supports the analysis of various genetic variants, including single nucleotide variants (SNVs), insertions and deletions (indels), copy number changes, fusions, and rearrangements. It offers flexible and automatable interpretation workflows, powered by QIAGEN's proprietary knowledge base, and integrates seamlessly with laboratory information management systems (LIMS) to scale up case processing. QCI Interpret is utilized by clinical labs worldwide to enhance the efficiency and accuracy of variant interpretation and reporting, particularly in oncology and hereditary disease applications. The platform has been trusted to analyze and interpret over 4 million NGS patient test cases globally, underscoring its reliability and effectiveness in clinical settings.

Api Available

yes

Certifications

• FDA 510(k)
• CE/MDR
• ONC
• ISO

Company Founding

1986

Company Offices

• Netherlands
• United States
• Germany
• United Kingdom
• France
• China
• Japan
• India
• Australia
• Brazil

Compliance

• HIPAA
• GDPR
• ISO 27001

Customers

Data Residency

US/EU regions

Data Standards

• FHIR
• HL7 v2
• DICOM
• SNOMED
• ICD-10

Deployment Model

• SaaS
• on_prem
• hybrid

Features

• Flexible and automatable interpretation workflows
• Interpretation of small variants (SNVs, indels, duplications, frameshifts)
• Exon-level and larger copy number changes interpretation
• Fusion and rearrangement analysis
• Tumor Mutational Burden (TMB) and Microsatellite Instability (MSI) assessment
• Preconfigured workflows for QIAGEN and commercial NGS panels
• Customizable reporting policies
• Automated variant reporting
• Drug and trial selection integration
• API integration with Laboratory Information Management Systems (LIMS)
• AI-driven literature extraction for rare disease genes
• Enhanced AI-trained phenotype-driven ranking of pathogenic variants
• Variant impact prediction tools (REVEL, SpliceAI)
• Bulk variant assessment
• Flagging of co-occurring variants
• Faster variant navigation
• Draft ACMG v4 & VICC points-based scoring guidance
• Somatic rereport treatment policy

Id

SW2567

Integration Partners

Integrations

• LIMS
• QIAGEN NGS panels
• Commercial NGS panels
• GeneReader NGS System
• QCI Secondary Analysis
• QCI Analyze

Languages Supported

• English
• German
• French
• Spanish
• Italian
• Dutch
• Chinese
• Japanese
• Korean
• Portuguese
• Russian
• Arabic
• Hindi
• Bengali
• Punjabi
• Javanese
• Turkish
• Vietnamese
• Telugu
• Marathi

Last Updated

2025-10-11

License

commercial

Market Segment

• enterprise
• smb

Optional Modules

• QCI Secondary Analysis
• QCI Analyze

Os Platforms

• Web

Pricing Details

Contact vendor for pricing information.

Pricing Model

subscription

Privacy Features

• BAA available
• Consent management
• Anonymization
• Data minimization

Product Code

SW2567

Product Name

QCI Interpret

Ratings

Regions Available

• North America
• Europe
• Asia
• Australia
• South America
• Africa

Related Urls

Release Year

Security Features

• Encryption
• RBAC
• SSO/SAML
• Audit logs
• 2FA
• DLP

Specialties

• Oncology
• Hereditary Diseases
• Genomics
• Bioinformatics
• Precision Medicine

Support Channels

System Requirements

Major OS/DB/hardware needs, or empty if SaaS-only

Target Users

• clinicians
• geneticists
• bioinformaticians
• laboratory technicians
• clinical researchers

Training Options

Type

product

User Reviews

Version

1.0

Alternatives

See related products

Canonical JSON

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  "product_name": "QCI Interpret",
  "company_name": "QIAGEN Digital Insights",
  "product_url": "https://www.qiagen.com/us/products/discovery-and-translational-research/next-generation-sequencing/informatics-and-data/interpretation-content-databases/qci-interpret/",
  "company_url": "https://www.qiagen.com/us/",
  "related_urls": [],
  "product_code": "SW2567",
  "summary": "QCI Interpret is a clinical decision support software by QIAGEN Digital Insights that enhances the interpretation and reporting of next-generation sequencing (NGS) data, improving turnaround times and diagnostic accuracy for high-throughput labs.",
  "description": "QCI Interpret is a clinical decision support software developed by QIAGEN Digital Insights, designed to streamline the interpretation and reporting of next-generation sequencing (NGS) data. It leverages advanced artificial intelligence (AI) capabilities, including AI-derived literature searches and AI-trained phenotype-driven ranking, to accelerate critical lab performance criteria such as turnaround time, diagnostic yield, and result quality. The software supports the analysis of various genetic variants, including single nucleotide variants (SNVs), insertions and deletions (indels), copy number changes, fusions, and rearrangements. It offers flexible and automatable interpretation workflows, powered by QIAGEN's proprietary knowledge base, and integrates seamlessly with laboratory information management systems (LIMS) to scale up case processing. QCI Interpret is utilized by clinical labs worldwide to enhance the efficiency and accuracy of variant interpretation and reporting, particularly in oncology and hereditary disease applications. The platform has been trusted to analyze and interpret over 4 million NGS patient test cases globally, underscoring its reliability and effectiveness in clinical settings.",
  "categories": [
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    "health Data Analytics",
    "genomics",
    "Clinical Decision Support",
    "Bioinformatics",
    "Genomic Data Analysis",
    "Variant Interpretation",
    "Clinical Reporting"
  ],
  "market_segment": [
    "enterprise",
    "smb"
  ],
  "target_users": [
    "clinicians",
    "geneticists",
    "bioinformaticians",
    "laboratory technicians",
    "clinical researchers"
  ],
  "specialties": [
    "Oncology",
    "Hereditary Diseases",
    "Genomics",
    "Bioinformatics",
    "Precision Medicine"
  ],
  "regions_available": [
    "North America",
    "Europe",
    "Asia",
    "Australia",
    "South America",
    "Africa"
  ],
  "languages_supported": [
    "English",
    "German",
    "French",
    "Spanish",
    "Italian",
    "Dutch",
    "Chinese",
    "Japanese",
    "Korean",
    "Portuguese",
    "Russian",
    "Arabic",
    "Hindi",
    "Bengali",
    "Punjabi",
    "Javanese",
    "Turkish",
    "Vietnamese",
    "Telugu",
    "Marathi"
  ],
  "pricing_model": "subscription",
  "pricing_details": "Contact vendor for pricing information.",
  "license": "commercial",
  "company_offices": [
    "Netherlands",
    "United States",
    "Germany",
    "United Kingdom",
    "France",
    "China",
    "Japan",
    "India",
    "Australia",
    "Brazil"
  ],
  "company_founding": "1986",
  "deployment_model": [
    "SaaS",
    "on_prem",
    "hybrid"
  ],
  "os_platforms": [
    "Web"
  ],
  "features": [
    "Flexible and automatable interpretation workflows",
    "Interpretation of small variants (SNVs, indels, duplications, frameshifts)",
    "Exon-level and larger copy number changes interpretation",
    "Fusion and rearrangement analysis",
    "Tumor Mutational Burden (TMB) and Microsatellite Instability (MSI) assessment",
    "Preconfigured workflows for QIAGEN and commercial NGS panels",
    "Customizable reporting policies",
    "Automated variant reporting",
    "Drug and trial selection integration",
    "API integration with Laboratory Information Management Systems (LIMS)",
    "AI-driven literature extraction for rare disease genes",
    "Enhanced AI-trained phenotype-driven ranking of pathogenic variants",
    "Variant impact prediction tools (REVEL, SpliceAI)",
    "Bulk variant assessment",
    "Flagging of co-occurring variants",
    "Faster variant navigation",
    "Draft ACMG v4 & VICC points-based scoring guidance",
    "Somatic rereport treatment policy"
  ],
  "optional_modules": [
    "QCI Secondary Analysis",
    "QCI Analyze"
  ],
  "integrations": [
    "LIMS",
    "QIAGEN NGS panels",
    "Commercial NGS panels",
    "GeneReader NGS System",
    "QCI Secondary Analysis",
    "QCI Analyze"
  ],
  "data_standards": [
    "FHIR",
    "HL7 v2",
    "DICOM",
    "SNOMED",
    "ICD-10"
  ],
  "api_available": "yes",
  "system_requirements": "Major OS/DB/hardware needs, or empty if SaaS-only",
  "compliance": [
    "HIPAA",
    "GDPR",
    "ISO 27001"
  ],
  "certifications": [
    "FDA 510(k)",
    "CE/MDR",
    "ONC",
    "ISO"
  ],
  "security_features": [
    "Encryption",
    "RBAC",
    "SSO/SAML",
    "Audit logs",
    "2FA",
    "DLP"
  ],
  "privacy_features": [
    "BAA available",
    "Consent management",
    "Anonymization",
    "Data minimization"
  ],
  "data_residency": "US/EU regions",
  "customers": [],
  "user_reviews": [],
  "ratings": [],
  "support_channels": [],
  "training_options": [],
  "release_year": "",
  "integration_partners": [],
  "id": "SW2567",
  "slug": "qci-interpret",
  "type": "product",
  "version": "1.0",
  "last_updated": "2025-10-11",
  "links_json": {
    "self": "https://www.healthaidb.com/software/qci-interpret.json"
  }
}