[Congressional Record Volume 171, Number 133 (Friday, August 1, 2025)]
[Senate]
[Pages S5465-S5467]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]

  SA 3670. Mr. YOUNG (for himself and Mr. Padilla) submitted an 
amendment intended to be proposed by him to the bill S. 2296, to 
authorize appropriations for fiscal year 2026 for military activities 
of the Department of Defense, for military construction, and for 
defense activities of the Department of Energy, to prescribe military 
personnel strengths for such fiscal year, and for other purposes; which 
was ordered to lie on the table; as follows:

       At the end of subtitle F of title X, insert the following:

     SEC. __. WEB OF BIOLOGICAL DATA.

       (a) Definitions.--In this section:
       (1) Advisory board.--The term ``advisory board'' means the 
     advisory board established under subsection (h).
       (2) Director.--The term ``Director'' means the Director of 
     the National Laboratory selected under subsection (b)(1)(A).
       (3) National laboratory.--The term ``National Laboratory'' 
     has the meaning given the term in section 2 of the Energy 
     Policy Act of 2005 (42 U.S.C. 15801).
       (4) Secretary.--The term ``Secretary'' means the Secretary 
     of Energy.
       (5) Web.--The term ``Web'' means the Web of Biological Data 
     established under subsection (b)(1)(A).

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       (b) Establishment.--
       (1) In general.--Not later than 180 days after the date of 
     enactment of this Act, the Secretary shall--
       (A) through a competitive process, award a grant to a 
     National Laboratory to establish a centralized data resource, 
     to be known as the ``Web of Biological Data'', to facilitate 
     biological research through advanced computational methods 
     such as artificial intelligence; and
       (B) establish a research and development program to further 
     data science relating to generating, storing, curating, and 
     managing biological data.
       (2) Contents.--The Web shall--
       (A) serve as a single point of entry for researchers to 
     access different sources of biological data, especially those 
     funded by the Federal Government, by directly hosting data or 
     providing access to existing databases;
       (B) have metrics and metadata to indicate data quality, 
     including usability, interoperability, and completeness; and
       (C) include tiered levels of cybersecurity safeguards and 
     access controls to protect different types of biological data 
     assets hosted in or connected to the Web.
       (c) Duties of Director.--As part of establishing the Web, 
     the Director may--
       (1) enter into data sharing agreements, memoranda of 
     understanding, or other relevant contracts with other Federal 
     departments and agencies to integrate biological datasets 
     into the Web that are not hosted by the Department of Energy;
       (2) enter into cost-sharing agreements with nongovernmental 
     entities to fund the Web;
       (3) establish partnerships with other Federal agencies, 
     academia, industry, and international partners and allies to 
     optimize usability and performance of the Web; and
       (4) carry out any other activities determined necessary by 
     the Secretary to advance United States biological data 
     curation and sharing.
       (d) Implementation Plan.--Not later than 1 year after the 
     date of enactment of this Act, the Director, in consultation 
     with the Secretary, shall submit to the Committee on Energy 
     and Natural Resources of the Senate and the Committee on 
     Energy and Commerce of the House of Representatives an 
     implementation plan for the Web that describes--
       (1) how the Director and the Secretary shall implement this 
     section;
       (2) a plan for working with Federal agencies--
       (A) to acquire data that was collected through Federal 
     funding; and
       (B) to digitize biological samples that are currently owned 
     or funded by the Federal Government;
       (3) the type of initial projects that shall be pursued 
     under the program established under subsection (b)(1)(B);
       (4) a plan for exploring and implementing cost-sharing 
     agreements, including with philanthropy and industry, to 
     assist in cost-sharing for the Web;
       (5) a cybersecurity plan for the Web; and
       (6) how the Director will leverage partnerships with other 
     Federal agencies, academia, and industry.
       (e) Phase I.--Not later than 2 years after the date of 
     enactment of this Act, the Director shall--
       (1) test an initial version of the Web, which shall--
       (A) focus on specific biological data subtypes selected in 
     consultation with the advisory board, representatives from 
     other Federal departments and agencies, and external 
     stakeholders from industry and academia;
       (B) include a single point-of-entry interface for 
     biological data that--
       (i) optimizes user experience and data management;
       (ii) is built around human-centered design principles;
       (iii) is built with the capability to expand to other 
     datasets and biological datatypes beyond the initial version; 
     and
       (iv) is built with tiered security access;
       (C) include initial frameworks, developed in collaboration 
     with the National Institute of Standards and Technology, for 
     application programming interfaces focusing on hosting an 
     initial list of biological data subtypes; and
       (D) include appropriate cybersecurity and access safeguards 
     to protect data accessible by the Web, including limiting 
     access to adversarial countries and countries that do not 
     participate in reciprocal data sharing, as determined by the 
     Secretary;
       (2) as part of developing the initial version of the Web 
     described in paragraph (1)--
       (A) work with Federal agencies to acquire data that was 
     collected through Federal funding;
       (B) develop cost-sharing agreements, including with 
     philanthropic and industry members, to fund the Web; and
       (C) work with biotechnology stakeholders to test and 
     evaluate the initial version and implement any needed changes 
     to ensure usability;
       (3) select initial research projects to fund under the 
     research and development program established under subsection 
     (b)(1)(B); and
       (4) submit a report to the committees described in 
     subsection (j) on the implementation of this subsection and 
     plans for carrying out subsection (f).
       (f) Phase II.--
       (1) In general.--Not later than 5 years after the date of 
     enactment of this Act, the Director shall expand the Web--
       (A) to be accessible to United States researchers;
       (B) to accommodate different types of biological data; and
       (C) to be capable of adapting and expanding based on the 
     emergence of new biological data.
       (2) Features.--The expanded version of the Web described in 
     paragraph (1) shall have the following features:
       (A) A fully realized single point-of-entry interface that--
       (i) is connected to any dataset or database that hosts 
     federally funded data;
       (ii) hosts biological data not already stored by other 
     Federal databases; and
       (iii) hosts relevant bioinformatic tools for optimized 
     access and analysis.
       (B) A full suite of interoperability frameworks associated 
     with different types of biological data, metadata, and 
     appropriate ontologies.
       (C) An online interface that optimizes usability, including 
     the ability to rapidly search through metadata across 
     databases.
       (D) Incorporation of human-centered design principles into 
     user interfaces.
       (E) A standard quality and format for the hosted biological 
     data that is appropriate for training artificial intelligence 
     models.
       (F) Restrictions on data sharing with countries described 
     in subsection (e)(1)(D).
       (G) Appropriate cybersecurity requirements and tiered 
     safeguards related to the sensitivity of data to prevent 
     misuse of data.
       (3) Other activities.--In the 3-year period following the 
     2-year period described in subsection (e), the Secretary 
     shall continue--
       (A) to carry out the activities described in subparagraphs 
     (A) and (B) of paragraph (2) of that subsection; and
       (B) to carry out the research and development program 
     established under subsection (b)(1)(B).
       (g) Independent Assessment of Cybersecurity.--The Director 
     shall seek to enter into a contract with an external entity 
     to conduct a biannual independent assessment of the 
     cybersecurity safeguards and access controls of the Web.
       (h) Advisory Board.--
       (1) In general.--Not later than 180 days after the 
     Secretary selects a National Laboratory under subsection 
     (b)(1)(A), the Secretary shall establish an advisory board to 
     oversee the implementation of the Web and ensure that the Web 
     maximizes the usability of biological datasets across 
     sectors.
       (2) Chair.--The Chair of the advisory board shall be the 
     Director.
       (3) Members.--The advisory board shall consist of 12 
     members, of whom--
       (A) 4 shall be representatives of industry;
       (B) 2 shall be representatives of academia;
       (C) 2 shall be representatives of National Laboratories 
     (excluding the National Laboratory selected under subsection 
     (b)(1)(A)); and
       (D) 3 shall be representatives of relevant Federal 
     departments and agencies, as determined by the Director.
       (4) FACA exemption.--Chapter 10 of title 5, United States 
     Code, shall not apply to the advisory board.
       (i) Collaboration.--In developing the Web, the Director 
     shall collaborate with--
       (1) Federal departments and agencies involved in biosafety 
     and biosecurity capabilities to assist with implementation of 
     proper cybersecurity and biosecurity safeguards;
       (2) the National Artificial Intelligence Research Resource 
     of the National Science Foundation to ensure integration of 
     well-curated biological data with cutting-edge foundational 
     artificial intelligence tools;
       (3) the National Institute of Standards and Technology to 
     ensure that--
       (A) the data included in the Web is formatted in a way that 
     is appropriate for training artificial intelligence models; 
     and
       (B) associated application programming interfaces and 
     ontologies are sufficiently adaptable to changes in 
     biological data;
       (4) the National Library of Medicine to ensure 
     compatibility and interoperability between the National 
     Center for Biotechnology information databases and the Web;
       (5) a nongovernmental group that is qualified to implement 
     an online interface that maximizes usability by the public 
     and human-centered design; and
       (6) any other Federal departments and agencies determined 
     relevant by the Director.
       (j) Report.--Not later than 2 years after the date of 
     enactment of this Act, and annually thereafter, the Director 
     shall submit to the Committee on Energy and Natural Resources 
     of the Senate and the Committee on Energy and Commerce of the 
     House of Representatives a report describing--
       (1) progress made in developing the Web, including--
       (A) the quantity of data stored directly on the Web and 
     accessible through application programming interfaces;
       (B) collaborations with other Federal agencies and 
     department; and
       (C) user engagement;
       (2)(A) any cybersecurity vulnerabilities identified by an 
     assessment carried out pursuant to subsection (g); and
       (B) actions taken to address those vulnerabilities; and
       (3) plans for maintenance, expansion, and development of 
     the Web in the subsequent year.
       (k) Authorization of Appropriations.--There are authorized 
     to be appropriated--
       (1) $50,000,000 for each of the first 2 years following the 
     date of enactment of this Act to carry out subsection (e); 
     and

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       (2) on completion of subsection (e) and the submission of 
     the report described in paragraph (4) of that subsection, 
     $200,000,000 for each of the subsequent 3 years to carry out 
     this section.
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