SureSeq NGS panels

JSON twin: https://www.healthaidb.com/software/sureseq-ngs-panels.json

Company Name

Oxford Gene Technology

Product URL

https://www.ogt.com/us/products/technology/sureseq-ngs

Company URL

https://www.ogt.com

Categories

• diagnostic Support
• genomics
• research
• Diagnostic
• Genetic Testing
• Cancer Research
• Genetic Disorders
• Next-generation Sequencing

Summary

SureSeq NGS panels by Oxford Gene Technology offer comprehensive next-generation sequencing solutions for various genetic analyses, including cancer research and genetic disorders.

Description

Oxford Gene Technology's SureSeq NGS panels provide a range of next-generation sequencing solutions designed for comprehensive genetic analyses. These panels are optimized for detecting low-frequency single nucleotide variants (SNVs), insertions and deletions (indels), and complex structural aberrations such as internal tandem duplications (ITDs), partial tandem duplications (PTDs), copy number variations (CNVs), loss of heterozygosity (LOH), and translocations. The panels are available in pre-designed formats and can be customized to target specific genes of interest, facilitating efficient and accurate genomic profiling. They are compatible with various sequencing platforms and are supported by OGT's Interpret NGS Analysis Software for streamlined data analysis.

Api Available

yes

Certifications

• FDA 510(k)
• CE/MDR
• ONC
• ISO

Company Founding

1995

Company Offices

• United Kingdom
• United States
• Germany
• France
• Italy
• Spain
• Netherlands
• Sweden
• Denmark
• Norway

Compliance

• HIPAA
• GDPR
• HITECH
• SOC 2
• ISO 27001

Customers

Data Residency

US/EU regions

Data Standards

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

Deployment Model

• SaaS
• on_prem
• hybrid

Features

• Comprehensive NGS panels for myeloid disorders
• Detection of SNVs, indels, ITDs, PTDs
• High coverage uniformity for low-frequency variants
• Streamlined library preparation workflow
• Integration with QIAGEN Clinical Insight (QCI) Interpret software
• Optimized for Illumina sequencing platforms
• Ready-to-use Universal Hyb & Wash buffer
• Unique Dual Index (UDI) and Unique Molecular Index (UMI) adapters
• Compatible with formalin-fixed paraffin-embedded (FFPE) samples
• Comprehensive bioinformatics support
• Customizable panel design for specific targets
• Enhanced detection in difficult-to-sequence regions
• Rapid sample-to-sequencer turnaround time
• Reduced hands-on time by up to 40%
• Comprehensive variant interpretation and reporting
• Support for hematology, solid tumor, and constitutional cytogenetics
• Pre-designed and custom NGS solutions
• Expert-curated gene selection for cancer panels
• High sensitivity in detecting complex structural aberrations

Id

SW2568

Integration Partners

Integrations

• QIAGEN Clinical Insight (QCI) Interpret software
• Illumina sequencing platforms

Languages Supported

• English
• Spanish
• French
• German
• Italian
• Portuguese
• Dutch
• Russian
• Chinese
• Japanese
• Korean
• Arabic
• Hindi
• Bengali
• Punjabi
• Telugu
• Marathi
• Tamil
• Urdu
• Gujarati

Last Updated

2025-10-11

License

commercial

Market Segment

• enterprise
• smb
• consumer

Optional Modules

• SureSeq Myeloid Plus Panel
• Universal NGS Complete Workflow Solution
• SureSeq Interpret Software
• SureSeq FFPE DNA Repair Mix
• SureSeq CLL + CNV V3 NGS Panel
• SureSeq Myeloid Fusion NGS Panel
• SureSeq Myeloid MRD NGS Panel
• SureSeq NGS Library Preparation Kit for solid tumor samples
• SureSeq NGS Library Preparation Kit for constitutional samples
• SureSeq NGS Library Preparation Kit for rare disease samples

Os Platforms

• Web
• iOS
• Android
• Windows
• macOS
• Linux

Pricing Details

Contact vendor for pricing information.

Pricing Model

subscription

Privacy Features

• BAA available
• consent mgmt
• anonymization
• data minimization

Product Code

SW2568

Product Name

SureSeq NGS panels

Ratings

Regions Available

• United States
• United Kingdom
• European Union
• Canada
• Australia
• Japan
• China
• India
• Brazil
• South Africa
• South Korea
• Mexico
• Russia
• Saudi Arabia
• United Arab Emirates
• Singapore
• Malaysia
• Thailand
• Indonesia
• Philippines

Related Urls

Release Year

Security Features

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

Specialties

• Oncology
• Hematology
• Genetic Disorders
• Cardiology
• Neurology
• Endocrinology
• Gastroenterology
• Pulmonology
• Infectious Diseases
• Immunology
• Dermatology
• Rheumatology
• Nephrology
• Ophthalmology
• Obstetrics And Gynecology
• Pediatrics
• Geriatrics
• Orthopedics
• Urology
• Otolaryngology

Support Channels

System Requirements

Illumina sequencing platforms

Target Users

• clinicians
• researchers
• geneticists
• laboratory technicians

Training Options

Type

product

User Reviews

Version

1.0

Alternatives

See related products

Canonical JSON

{
  "product_name": "SureSeq NGS panels",
  "company_name": "Oxford Gene Technology",
  "product_url": "https://www.ogt.com/us/products/technology/sureseq-ngs",
  "company_url": "https://www.ogt.com",
  "related_urls": [],
  "product_code": "SW2568",
  "summary": "SureSeq NGS panels by Oxford Gene Technology offer comprehensive next-generation sequencing solutions for various genetic analyses, including cancer research and genetic disorders.",
  "description": "Oxford Gene Technology's SureSeq NGS panels provide a range of next-generation sequencing solutions designed for comprehensive genetic analyses. These panels are optimized for detecting low-frequency single nucleotide variants (SNVs), insertions and deletions (indels), and complex structural aberrations such as internal tandem duplications (ITDs), partial tandem duplications (PTDs), copy number variations (CNVs), loss of heterozygosity (LOH), and translocations. The panels are available in pre-designed formats and can be customized to target specific genes of interest, facilitating efficient and accurate genomic profiling. They are compatible with various sequencing platforms and are supported by OGT's Interpret NGS Analysis Software for streamlined data analysis.",
  "categories": [
    "diagnostic Support",
    "genomics",
    "research",
    "Diagnostic",
    "Genetic Testing",
    "Cancer Research",
    "Genetic Disorders",
    "Next-generation Sequencing"
  ],
  "market_segment": [
    "enterprise",
    "smb",
    "consumer"
  ],
  "target_users": [
    "clinicians",
    "researchers",
    "geneticists",
    "laboratory technicians"
  ],
  "specialties": [
    "Oncology",
    "Hematology",
    "Genetic Disorders",
    "Cardiology",
    "Neurology",
    "Endocrinology",
    "Gastroenterology",
    "Pulmonology",
    "Infectious Diseases",
    "Immunology",
    "Dermatology",
    "Rheumatology",
    "Nephrology",
    "Ophthalmology",
    "Obstetrics And Gynecology",
    "Pediatrics",
    "Geriatrics",
    "Orthopedics",
    "Urology",
    "Otolaryngology"
  ],
  "regions_available": [
    "United States",
    "United Kingdom",
    "European Union",
    "Canada",
    "Australia",
    "Japan",
    "China",
    "India",
    "Brazil",
    "South Africa",
    "South Korea",
    "Mexico",
    "Russia",
    "Saudi Arabia",
    "United Arab Emirates",
    "Singapore",
    "Malaysia",
    "Thailand",
    "Indonesia",
    "Philippines"
  ],
  "languages_supported": [
    "English",
    "Spanish",
    "French",
    "German",
    "Italian",
    "Portuguese",
    "Dutch",
    "Russian",
    "Chinese",
    "Japanese",
    "Korean",
    "Arabic",
    "Hindi",
    "Bengali",
    "Punjabi",
    "Telugu",
    "Marathi",
    "Tamil",
    "Urdu",
    "Gujarati"
  ],
  "pricing_model": "subscription",
  "pricing_details": "Contact vendor for pricing information.",
  "license": "commercial",
  "company_offices": [
    "United Kingdom",
    "United States",
    "Germany",
    "France",
    "Italy",
    "Spain",
    "Netherlands",
    "Sweden",
    "Denmark",
    "Norway"
  ],
  "company_founding": "1995",
  "deployment_model": [
    "SaaS",
    "on_prem",
    "hybrid"
  ],
  "os_platforms": [
    "Web",
    "iOS",
    "Android",
    "Windows",
    "macOS",
    "Linux"
  ],
  "features": [
    "Comprehensive NGS panels for myeloid disorders",
    "Detection of SNVs, indels, ITDs, PTDs",
    "High coverage uniformity for low-frequency variants",
    "Streamlined library preparation workflow",
    "Integration with QIAGEN Clinical Insight (QCI) Interpret software",
    "Optimized for Illumina sequencing platforms",
    "Ready-to-use Universal Hyb & Wash buffer",
    "Unique Dual Index (UDI) and Unique Molecular Index (UMI) adapters",
    "Compatible with formalin-fixed paraffin-embedded (FFPE) samples",
    "Comprehensive bioinformatics support",
    "Customizable panel design for specific targets",
    "Enhanced detection in difficult-to-sequence regions",
    "Rapid sample-to-sequencer turnaround time",
    "Reduced hands-on time by up to 40%",
    "Comprehensive variant interpretation and reporting",
    "Support for hematology, solid tumor, and constitutional cytogenetics",
    "Pre-designed and custom NGS solutions",
    "Expert-curated gene selection for cancer panels",
    "High sensitivity in detecting complex structural aberrations"
  ],
  "optional_modules": [
    "SureSeq Myeloid Plus Panel",
    "Universal NGS Complete Workflow Solution",
    "SureSeq Interpret Software",
    "SureSeq FFPE DNA Repair Mix",
    "SureSeq CLL + CNV V3 NGS Panel",
    "SureSeq Myeloid Fusion NGS Panel",
    "SureSeq Myeloid MRD NGS Panel",
    "SureSeq NGS Library Preparation Kit for solid tumor samples",
    "SureSeq NGS Library Preparation Kit for constitutional samples",
    "SureSeq NGS Library Preparation Kit for rare disease samples"
  ],
  "integrations": [
    "QIAGEN Clinical Insight (QCI) Interpret software",
    "Illumina sequencing platforms"
  ],
  "data_standards": [
    "FHIR",
    "HL7 v2",
    "DICOM",
    "SNOMED",
    "ICD-10"
  ],
  "api_available": "yes",
  "system_requirements": "Illumina sequencing platforms",
  "compliance": [
    "HIPAA",
    "GDPR",
    "HITECH",
    "SOC 2",
    "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 mgmt",
    "anonymization",
    "data minimization"
  ],
  "data_residency": "US/EU regions",
  "customers": [],
  "user_reviews": [],
  "ratings": [],
  "support_channels": [],
  "training_options": [],
  "release_year": "",
  "integration_partners": [],
  "id": "SW2568",
  "slug": "sureseq-ngs-panels",
  "type": "product",
  "version": "1.0",
  "last_updated": "2025-10-11",
  "links_json": {
    "self": "https://www.healthaidb.com/software/sureseq-ngs-panels.json"
  }
}