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  • Ginkgo Bioworks Selected by PNNL to Deliver a Modular, High‑Throughput Phenotyping Platform for DOE’s M2PC

    Ginkgo Bioworks Selected by PNNL to Deliver a Modular, High‑Throughput Phenotyping Platform for DOE’s M2PC

    BOSTON, Dec. 5, 2025 /PRNewswire/ — Ginkgo Bioworks (NYSE: DNA) today announced it has been awarded by the Environmental Molecular Sciences Laboratory (EMSL) at Pacific Northwest National Laboratory (PNNL) a four-year, up to $47M contract to co-design, build, and integrate a High‑Throughput Automated Phenotyping Platform (HTP‑APP) in support of the Microbial Molecular Phenotyping Capability (M2PC). The platform, selected through a competitive procurement process, is intended to enable the Department of Energy’s (DOE) Office of Science, Biological and Environmental Research program to generate rich, reproducible microbial and microbiome data that ensure the U.S. remains at the forefront of the bioeconomy, safeguarding economic, societal, and national security benefits while maintaining global leadership in biotechnology innovation.

    Drawing on Ginkgo Automation’s dynamic Catalyst scheduling software and modular Reconfigurable Automation Carts (RACs), the HTP‑APP is designed to automate end‑to‑end workflows—from media and cultivation to sample preparation and multimodal analytics—while supporting BSL‑2 operations, remote planning and execution, and laboratory integration. This modular approach is expected to help PNNL adapt the platform as scientific needs evolve, add new methods or instrumentation, and maintain high uptime in a user‑facility environment. Conceptual design elements include a RAC‑based architecture with function‑oriented “pods,” integrated transport, and software‑enabled interleaving of diverse protocols.

    “Our team is excited to contract and collaborate with PNNL again to build a new capability we believe will expand access to high‑quality biological phenotyping at scale. By combining modular automation with flexible software and managed support, we aim to help researchers generate the datasets that modern AI methods need,” said Will Serber, General Manager of Ginkgo Automation.

    “The recent AI Action Plan from President Trump called for investment in AI-enabled cloud laboratories to accelerate U.S. scientific innovation. This new project is a powerful example of how Ginkgo’s AI-enabled cloud lab technology can help keep the American bioeconomy competitive globally,” added Jason Kelly, CEO of Ginkgo Bioworks.

    M2PC is focused on delivering a predictive understanding of complex biological systems relevant to DOE’s mission. The planned platform is intended to (i) increase throughput and reproducibility of phenotyping campaigns across diverse microbes and consortia, (ii) capture multimodal analytical measurements suitable for AI/ML, and (iii) provide a sustainable, expandable foundation for future instrumentation and workflows at PNNL’s EMSL.

    More information about RACs and Catalyst automation software can be found here or at automation.ginkgo.bio.

    Planned platform highlights

    • Modularity and expandability: RAC‑based hardware that can be reconfigured or scaled as needs change; software “digital twin” tools to model throughput and identify bottlenecks.
    • End‑to‑end workflow coverage: Media prep, cultivation (including photosynthetic workflows), sample prep, and multimodal analytics (e.g., plate readers, imaging, flow cytometry, and LC/GC‑MS modalities) designed to support high‑quality, multimodal data generation.
    • Operations and reliability: Designed for cloud lab-ready remote monitoring and safe recovery, with training and managed support to help maximize uptime in a national user‑facility setting.

    About Ginkgo Bioworks

    Ginkgo Bioworks builds the tools that make biology easier to engineer for everyone. Ginkgo R&D Solutions delivers customizable R&D packages—such as protein engineering, nucleic acid design, and cell-free systems—giving partners a comprehensive way to accelerate innovation across therapeutics, diagnostics, & manufacturing. Ginkgo Agriculture provides R&D services for innovative companies that are developing agricultural biologicals and novel plant traits, including lead discovery, characterization and validation, product & process co-development, and small-scale toll manufacturing. Ginkgo Automation sells modular, integrated laboratory automation so scientists can spend their days planning and analyzing experiments rather than pipetting in the lab. Ginkgo Datapoints uses Ginkgo’s in-house automation to generate the large lab data sets to power your AI models. Ginkgo Biosecurity is building and deploying the next-generation infrastructure and technologies that global leaders need to predict, detect, and respond to a wide variety of biological threats. For more information, visit ginkgobioworks.com and ginkgobiosecurity.com, read our blog, or follow us on social media channels such as X (@Ginkgo and @Ginkgo_Biosec), Instagram (@GinkgoBioworks), Threads (@GinkgoBioworks), or LinkedIn.

    Forward-Looking Statements of Ginkgo Bioworks

    This press release contains certain forward-looking statements within the meaning of the federal securities laws, including statements regarding the capabilities and potential success of the partnership and Ginkgo’s cell programming platform. These forward-looking statements generally are identified by the words “believe,” “can,” “project,” “potential,” “expect,” “anticipate,” “estimate,” “intend,” “strategy,” “future,” “opportunity,” “plan,” “may,” “should,” “will,” “would,” “will be,” “will continue,” “will likely result,” and similar expressions. Forward-looking statements are predictions, projections and other statements about future events that are based on current expectations and assumptions and, as a result, are subject to risks and uncertainties. Many factors could cause actual future events to differ materially from the forward-looking statements in this press release, including but not limited to: (i) our ability to realize near-term and long-term cost savings associated with our site consolidation plans, including the ability to terminate leases or find sub-lease tenants for unused facilities, (ii) volatility in the price of Ginkgo’s securities due to a variety of factors, including changes in the competitive and highly regulated industries in which Ginkgo operates and plans to operate, variations in performance across competitors, and changes in laws and regulations affecting Ginkgo’s business, (iii) the ability to implement business plans, forecasts, and other expectations, and to identify and realize additional business opportunities, including with respect to our solutions and tools offerings, (iv) the risk of downturns in demand for products using synthetic biology, (v) the uncertainty regarding the demand for passive monitoring programs and biosecurity services, (vi) changes to the biosecurity industry, including due to advancements in technology, emerging competition and evolution in industry demands, standards and regulations, (vii) the outcome of any pending or potential legal proceedings against Ginkgo, (viii) our ability to realize the expected benefits from and the success of our Foundry platform programs and Codebase assets, (ix) our ability to successfully develop engineered cells, bioprocesses, data packages or other deliverables, (x) the product development, production or manufacturing success of our customers, (xi) our exposure to the volatility and liquidity risks inherent in holding equity interests in other operating companies and other non-cash consideration we may receive for our services, (xii) the potential negative impact on our business of our restructuring or the failure to realize the anticipated savings associated therewith and (xiii) the uncertainty regarding government budgetary priorities and funding allocated to government agencies. The foregoing list of factors is not exhaustive. You should carefully consider the foregoing factors and the other risks and uncertainties described in the “Risk Factors” section of Ginkgo’s annual report on Form 10-K filed with the U.S. Securities and Exchange Commission (the “SEC”) on February 25, 2025 and other documents filed by Ginkgo from time to time with the SEC. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements. Forward-looking statements speak only as of the date they are made. Readers are cautioned not to put undue reliance on forward-looking statements, and Ginkgo assumes no obligation and does not intend to update or revise these forward-looking statements, whether as a result of new information, future events, or otherwise. Ginkgo does not give any assurance that it will achieve its expectations.

    GINKGO BIOWORKS INVESTOR CONTACT:
    [email protected]

    GINKGO BIOWORKS MEDIA CONTACT:
    [email protected]

    SOURCE Ginkgo Bioworks


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  • Homeland security head reveals plans to widen US travel ban to more than 30 countries | US immigration

    Homeland security head reveals plans to widen US travel ban to more than 30 countries | US immigration

    The US plans to expand the number of countries covered by its travel ban to more than 30, the secretary of the Department of Homeland Security (DHS), Kristi Noem, has announced.

    Noem, in an interview on Fox News’s The Ingraham Angle on Thursday…

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  • Five-star Saqib helps Karachi Blues crush Sialkot to win QEAT 2025

    Five-star Saqib helps Karachi Blues crush Sialkot to win QEAT 2025

    LAHORE: Abdullah Fazal and Haroon Arshad’s sparkling centuries, backed by a splendid bowling display from pacer Saqib Khan — who took a five-wicket haul in the second innings and nine in the match — helped Karachi Blues clinch the…

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  • Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 2-4 December 2025

    CVMP opinions on veterinary medicinal products

    The Committee adopted a positive opinion for a marketing authorisation from Elanco GmbH for Varenzin (molidustat), for the management of non-regenerative anaemia associated with chronic kidney disease (CKD) in cats, by increasing haematocrit/ packed cell volume.

    The Committee adopted a positive opinion, in exceptional circumstances, for a marketing authorisation from Laboratorios Syva S.A. for Epizootic haemorrhagic disease vaccine for the active immunisation of cattle to reduce viraemia and fever caused by epizootic haemorrhagic disease virus serotype 8.

    The Committee adopted a positive opinion for a marketing authorisation from CP-Pharma Handelsgesellschaft mbH for Firocoxib CP-Pharma (firocoxib), for the relief of pain and inflammation associated with osteoarthritis and for the relief of post-operative pain and inflammation associated with soft-tissue, orthopaedic and dental surgery in dogs.

    The Committee adopted a positive opinion for a variation for Dexdomitor (dexmedetomidine) concerning change(s) to therapeutic indication(s) – addition of a new therapeutic indication or modification of an approved one for Dexdomitor 0.5 mg/ml solution for injection: to be administered intravenously as a constant rate infusion in dogs and cats as part of a multimodal protocol during inhalation anaesthesia.

    The Committee adopted a positive opinion for a variation for Felpreva (meloxicam) to change the frequency of the adverse event “Application site reaction (e.g. scratching, erythema, hair loss, inflammation)” from very rare to rare.

    The Committee adopted a positive opinion for a variation to align the product information with version 9.1 of the QRD template for Mirataz.

    The Committee adopted positive opinions for variation applications concerning quality-related (manufacturing) changes for:

    • AdTab
    • Dexdomitor
    • Duotic/ Osurnia
    • Eluracat
    • Meloxidyl
    • Nexgard / Nexgard Spectra / Frontpro
    • ProteqFlu – Te Equine influenza (live recombinant) and tetanus vaccine
    • Sileo
    • Zuprevo

    Withdrawals of applications

    The Committee was informed of the formal notification from Vetbiobank of their decision to withdraw the application for an initial marketing authorisation for Livencia. More information about this application and the state of the scientific assessment at the time of the withdrawal will be made available in a public assessment report. The document, together with the withdrawal letter from the applicant, will be published on the Agency’s website in due course.

    Union referrals and related procedures

    The Committee concluded the procedure for Phenoxypen WSP, 325 mg/g powder for use in drinking water for chickens (phenoxymethylpenicillin) from Dopharma Research B.V. The European Commission (EC) had requested clarifications from the Committee under Article 54(8) of Regulation (EU) 2019/6 on a variation requiring assessment, due to lack of consensus between Member States in the CMDv review procedure on grounds of efficacy. The CVMP, having considered the request by the EC and all available data, concluded, by majority, that the benefit-risk balance of Phenoxypen WSP for the proposed indication and target species is positive, provided some amendments are implemented as outlined in the CVMP opinion.

    Maximum residue limits

    Further to a request from the European Commission, the Committee adopted, by consensus, a positive opinion recommending the modification of maximum residue limits for lidocaine in porcine species, to allow for the injection into the scrotum, testicles and spermatic cord in piglets up to 7 days of age. Lidocaine is currently included in Table 1 (Allowed substances) of the Annex to Commission Regulation (EU) No 37/2010 with a ‘No MRL required’ classification for porcine but only for cutaneous and epilesional use.

    Scientific advice

    The Committee adopted seven scientific advice reports following requests for initial advice for two pharmaceutical products, three biological products and two immunological products for cattle (2), Atlantic salmon (1), horses (1), dogs (2) and pigs (1).

    Limited market classifications and eligibility according to Article 23 of Regulation (EU) 2019/6

    Following two requests, the CVMP classified:

    • A product (ATCvet classification: alimentary tract and metabolism) for horses as intended for a limited market and eligible for authorisation under Article 23 of Regulation (EU) 2019/6.
    • A product (ATCvet classification: musculo-skeletal system) for horses as intended for a limited market and eligible for authorisation under Article 23 of Regulation (EU) 2019/6.

    Pharmacovigilance

    The Committee adopted the outcomes of the signal management process for the current month. The signals submitted by marketing authorisation holders are listed, in chronological order, in the IRIS public portal: List of signals from Veterinary Signal Management. In order to access the list, the following filter should be applied in the ‘Submission type’ category: ‘Signal management submission’.

    Concept papers, guidelines

    Quality

    The Committee adopted a guideline on development and manufacture of synthetic peptides. This guideline has been developed to address specific aspects regarding the manufacturing process, characterisation, specifications and analytical control for synthetic peptides which are not covered in the Guideline on the Chemistry of Active Substances (EMA/454576/2016) or Chemistry of Active Substances for Veterinary Medicinal Products (EMA/CVMP/QWP/707366/2017). It also contains requirements and considerations related to conjugation, to medicinal product development, to synthetic peptide development using biological peptides as European reference medicinal product, and to clinical trial applications (human products only). The guideline will come into effect on 1 June 2026.

    Antimicrobial resistance

    Under Regulation (EU) 2019/6, the collection of data on sales of veterinary antimicrobials and on the use of antimicrobials in animals became a mandatory activity for Member States, who are obliged to report this data to the EMA. The Agency, in turn, cooperates with Member States to publish an annual report on the data.

    This month, the Committee adopted the second European Sales and Use of Antimicrobials for veterinary medicine (ESUAvet) report, which constitutes the annual surveillance report for 2024. It will be published on the EMA website on 9 December 2025.

    Organisational matters

    The Committee adopted the CVMP work plan for 2026.

    Working parties

    The Committee adopted the AWP, ERAWP, ESUAvet, EWP-V, IWP-V, NTWP, PhVWP-V, SAWP-V, SWP-V work plans for 2026, and the QWP, 3RsWP 3-year work plans for 2026-2028.

    More information about the above-mentioned medicines (including their full indications), guidelines, reflection papers, questions and answers and other documents, such as overviews on comments received during consultation, can be found below in Related content.

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  • K-Electric, Bank Alfalah Expand Digital Payment Convenience with Cashback Offer – K-Electric

    K-Electric, Bank Alfalah Expand Digital Payment Convenience with Cashback Offer – K-Electric


    Karachi, December 5, 2025:
    K-Electric (KE) has partnered with Bank Alfalah to encourage digital bill payments through a limited-time cashback offer, enabling customers to save instantly while experiencing seamless and secure transactions. Under the campaign, customers paying their KE bills via Alfa app by scanning the QR code on their bill will receive PKR 500 cashback, applicable on bill amounts of PKR 5,000 and above.

    The initiative is part of KE’s ongoing commitment to strengthen digital adoption across its customer base. Over 2.7 million customers are currently digitally connected, nearly three-fourths of KE’s total customers. Of these, 1.9 million customers actively use digital banking channels for their monthly electricity payments, reflecting a strong shift toward convenient and cashless modes of engagement.

    Speaking about the collaboration, Noor Afshan, Head of Marketing & Customer Experience at KE, said: “Digital adoption is no longer an added convenience, it is central to how today’s customers want to manage their lives. At KE, we are continuously working with leading financial partners to make bill payments easier, faster, and more rewarding. This collaboration reinforces our focus on building a frictionless customer experience and strengthening the digital ecosystem for Karachi.”

    The steady rise in digital payments reflects how Karachi’s customers, across both urban and peri-urban areas, are increasingly opting for cashless, contactless, and convenient channels. KE continues to introduce digital solutions that make essential services easier to access, supporting a more convenient ecosystem where customers can engage, transact, and resolve queries with greater ease.

    About K-Electric:
    K-Electric (KE) is a public listed company incorporated in Pakistan in 1913 as KESC. Privatized in 2005, KE is the only vertically integrated power utility in Pakistan supplying electricity to Karachi and its adjoining areas. The majority shares (66.4%) of the Company are owned by KES Power, a consortium of investors including Al-Jomaih Power Limited of Saudi Arabia, National Industries Group (Holding) of Kuwait, and KE Holdings (Formerly: Infrastructure and Growth Capital Fund or IGCF). The Government of Pakistan is also a shareholder (24.36%) in the Company while the remaining are listed as free float shares.

    www.ke.com.pk

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  • More than 10 children reportedly killed in attack on kindergarten in South Kordofan, Sudan – Unicef

    1. More than 10 children reportedly killed in attack on kindergarten in South Kordofan, Sudan  Unicef
    2. Sudan says RSF drone strike kills 79 civilians, including 43 children  The Express Tribune
    3. Residents say 40 killed in alleged army strike in southern…

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  • A culinary educator and local dining expert breaks down Michelin’s debut Philly list − and gives zero stars to the inspectors

    A culinary educator and local dining expert breaks down Michelin’s debut Philly list − and gives zero stars to the inspectors

    Working in restaurants is physically, mentally and emotionally taxing and often thankless work. So it was wonderful to see so many hardworking friends in the Philadelphia dining industry recognized at the Michelin Guide’s 2025 Northeast…

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  • Minecraft 1.21.11 Release Candidate 2

    Minecraft 1.21.11 Release Candidate 2

    Today we are shipping Release Candidate 2, fixing a crash issue affecting some players.

    Happy mining!

    Stability

    Get the Release Candidate

    Release Candidates are available for Minecraft: Java Edition. To install the Release Candidate,…

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  • ‘I’ve had all the luck you can get’: Michael Caine retires for the fourth time | Film

    ‘I’ve had all the luck you can get’: Michael Caine retires for the fourth time | Film

    Michael Caine has offered an update on his possible retirement from acting at the Red Sea international film festival in Saudi Arabia, appearing to call time on his career for the fourth time.

    Taking to the stage to accept a lifetime achievement…

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  • Controversial social media posts case: Imaan Mazari, Hadi Chatha submit list of defence witnesses – Pakistan

    Controversial social media posts case: Imaan Mazari, Hadi Chatha submit list of defence witnesses – Pakistan

    Lawyer Imaan Mazari and her spouse, Hadi Ali Chatha, on Friday handed over their list of defence witnesses as proceedings resumed in the controversial tweets case before Additional Sessions Judge Muhammad Afzal Majoka in the District and Sessions…

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