Sequence Listing Services

Transform your biological innovations into patent-ready documentation with our comprehensive sequence listing services. As a trusted partner to leading life sciences, healthcare, and pharmaceutical companies, we ensure your patent applications meet the highest standards of compliance and accuracy.

Expert Sequence Listing Solutions

Sequence listings are fundamental to patent applications involving biological sequences. Our specialized team handles all aspects of sequence documentation for:

  • Novel antibody developments
  • Innovative biomarker discoveries
  • Advanced oligonucleotide research
  • Groundbreaking peptide and DNA sequence innovations

Why Choose Our Sequence Lisitng Services?

Expert Sequence Listing Solutions

Our dedicated team of specialists combines deep regulatory knowledge with technical precision, ensuring your sequence listings meet all current international standards while protecting your intellectual property interests.

Comprehensive Compliance

We maintain strict adherence to both current and legacy standards:

  • Full compliance with WIPO Standard ST.26 for new applications
  • Support for legacy ST.25 format requirements
  • Perfect alignment with US 37 C.F.R. §§ 1.821-1.825
  • Seamless international patent office compatibility

Advanced Technical Infrastructure

We leverage industry-leading tools and technologies:

  • Latest WIPO Sequence database implementation
  • Validated PatentIn Version 3.5 software integration
  • Advanced BiSSAP processing capabilities
  • Multiple output format support including XML 1.0 with Unicode UTF-8 encoding

Strategic Value for Your Patent Portfolio

Global Recognition

Our sequence listings are structured for universal acceptance across:

  • All receiving Offices
  • International Searching Authorities
  • Preliminary Examining Authorities
  • National Phase Offices

Legal Protection

We understand the dual nature of sequence listings as both chemical compounds and information carriers, ensuring your documentation provides:

  • Robust patent eligibility support
  • Clear infringement analysis framework
  • Strong dispute resolution foundation

Our Process

1. Initial Consultation Understand your specific requirements and timeline

2. Technical Analysis Review your sequence data and determine optimal documentation approach

3. Documentation Development Create comprehensive sequence listings using appropriate standards

4. Quality Assurance Multiple verification steps to ensure accuracy and compliance

5. Delivery and Support Provide ready-to-file documentation with ongoing support

The Teak IP Advantage

When you choose our sequence listing services, you’re partnering with a leader in intellectual property documentation. Our commitment to excellence, combined with our technical expertise and understanding of regulatory requirements, ensures your biological innovations receive the protection they deserve.

Contact our team today to discuss how we can support your sequence listing needs and strengthen your patent portfolio.

Contact Us

Please fill out this form and a Teak IP Expert representative will be in touch shortly.

Exclusive Content / Knowledge Resources

White Papers

White Paper

The Hidden Costs of Non-Compliance: How Inadequate Sequence Listings Impact Patent Protection and Market Access

White Paper

Navigating Global Patent Filing: A Comprehensive Analysis of Sequence Listing Requirements Across Major Jurisdictions

Playbook

WIPO ST.26 Implementation: Strategic Considerations for Biotechnology Patent
Portfolios

Blueprint

Cross-Border Patent Strategy: Managing Sequence Listing Complexities in Multi-Jurisdictional Filings

Framework

The Sequence Listing Success Framework: A 5-Phase Methodology for Patent-Ready Submissions

Playbook

Biopharma Patent Filing Playbook: Strategic Sequence Management from Discovery to Grant

Toolkit

The Quality Assurance Toolkit for Sequence Listings: Templates, Checklists, and Validation Protocols

l

Client Success Stories

Client Success Story

Streamlining Patent Administration: A Mid-sized IP Law Firm Success Story

Client Success Story

Patent Docket Management Excellence: A Small Law Firm Success Story

Guides / Handbooks

Guide

The Complete Guide to WIPO ST.26 Compliance for Biotechnology Patents: Standards, Formats, and Best Practices

Guide

The Life Sciences IP Professional's Guide to International
Sequence Listing
Standards

Guide

The Biopharma Professional's Guide to Global Sequence Listing Requirements: USPTO, EPO, JPO, and Beyond

Handbook

Sequence Listing Handbook for Patent Attorneys: From Nucleotide Sequences to Successful Applications

Frequently Asked Questions – Sequence Listing Services

Q: What is Sequence Listing?

A: Sequence Listing is a standardized format for presenting DNA, RNA, and protein sequences in patent applications. It is specifically required for inventions involving:

  • Biomarkers
  • Antibodies
  • Oligonucleotides
  • Other peptide and DNA sequence-based innovations

Q: What are the current regulatory requirements for Sequence Listings?

A: Patent offices worldwide mandate sequence listings in standardized formats. For applications filed on or after July 1, 2022, the current standard (ST.26):

  • Requires XML format submission
  • Follows WIPO Standard ST.26 specifications
  • Is mandatory for all new patent applications containing sequence disclosures

Q: What about legacy applications filed before July 1, 2022?

A: Legacy applications follow Standard ST.25, which:

  • Continues to be valid for existing applications
  • Follows different formatting requirements
  • Must comply with US 37 C.F.R. §§ 1.821-1.825

Q: Why are Sequence Listings strategically important?

A: Sequence listings serve two critical purposes:

  1. Legal Framework:
    • They are recognized as both chemical compounds and information-encoding elements
    • Critical for patent eligibility determinations
    • Essential in infringement analysis and dispute resolution
  2. International Compatibility:
    • Creates a universally accepted format
    • Valid across all receiving Offices
    • Accepted by International Searching Authorities
    • Compliant with Preliminary Examining Authorities
    • Enables seamless transition to National Phase Offices

Q: What compliance standards do your services follow?

A: Our services ensure strict adherence to:

  • US regulations (37 CFR 1.831–1.835)
  • WIPO standard ST.26
  • US 37 C.F.R. §§ 1.821-1.825
  • WIPO standard ST.25

Q: What software infrastructure do you use?

A: We utilize industry-standard tools including:

  • WIPO Sequence database for ST.26-compliant listings
  • PatentIn Version 3.5 software (as referenced in MPEP § 2430)
  • BiSSAP for ST.25 format generation

Q: What output formats do you provide?

A: Our service delivers sequences in multiple formats:

  • XML 1.0 with Unicode UTF-8 encoding
  • WIPO Standard ST.26 DTD-compliant format
  • ASCII text format (compatible with Electronic Filing System)

Q: How do you ensure quality and compliance in your services?

A: We position ourselves as essential support for biotechnology patent applications by:

  • Maintaining strict compliance with all current international standards
  • Following rigorous quality control procedures
  • Staying updated with the latest regulatory requirements
  • Providing comprehensive documentation support

Q: Who can benefit from your Sequence Listing services?

A: Our services are particularly valuable for:

  • Life sciences companies
  • Healthcare organizations
  • Pharmaceutical companies
  • Biotechnology firms
  • Research institutions filing patent applications involving biological sequences

Q: What makes your Sequence Listing services unique?

A: Our services stand out through:

  • Comprehensive regulatory compliance
  • Expert technical implementation
  • Industry-standard software utilization
  • Multiple format support
  • Dedicated quality assurance

Contact Us

Please fill out this form and a Teak IP Expert representative will be in touch shortly.

Services Tailored to Your Needs

Tailored-Patent-TM-IP-solutions-to-fit-your-needs

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