DNAGinkgo+PlatformTWSTTwist+SynthesisABSIAbsci+AIDesignCRSPCRISPR Therapeutics+EditBEAMBeam+BaseEditNTLAIntellia+InVivoCRBUCaribou+CellTherapyRXRXRecursion+AIILMNIllumina+SeqEDITEditas+GeneFUND.YTD2025$17.3B.Raised

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Real-time intelligence on synbio and synbio funding, regulatory milestones, deployments, and policy.

Apr 16, 2026RESEARCH

Scientists Engineer DGR Systems for Targeted Hypermutagenesis in E.coli

Nature Biotechnology study demonstrates programmable diversity-generating retroelements for precise directed evolution

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Apr 15, 2026RESEARCH

Small-Molecule Base Editor Cuts Cancer Gene Screen Time 75%

New platform enables precise in vivo cancer gene screens with 4-fold reduced toxicity and temporal control

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Apr 15, 2026RESEARCH

iPSC Manufacturing Cuts NK Cell Therapy COGS by 65% vs Autologous

Universal master cell banks slash production costs and patient attrition in NK cell therapies

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Apr 15, 2026MARKET

Sumitomo Mitsui Dumps 217K Twist Bio Shares Worth $11M

Japanese trust giant reduces Twist position by 19% as DNA synthesis sector faces headwinds

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Apr 14, 2026BREAKING

Cellares Doses First Patients with Automated CAR-T Manufacturing

Cellares demonstrates scalable autologous cell therapy production with first patient dosings

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Apr 14, 2026BREAKING

CRISPR Silences Down Syndrome Chromosome in Breakthrough Study

Researchers demonstrate targeted silencing of extra chromosome 21 using CRISPR-based approach in Down syndrome cells

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Apr 14, 2026BREAKING

Baillie Gifford Increases Beam Therapeutics Stake by 40%

Edinburgh fund manager boosts position in base editing pioneer amid sector consolidation

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Apr 14, 2026MARKET

Evercore Raises Editas Price Target to $15 on CRISPR Pipeline

Evercore maintains Buy rating for Editas Medicine with increased $15 target amid CRISPR program momentum

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Apr 13, 2026BREAKING

Compact CRISPR System Fits Therapeutic Delivery Constraints

New miniaturized CRISPR platform addresses AAV packaging limits that constrain therapeutic genome editing applications

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Apr 13, 2026BREAKING

NIH Funds Ultra-Compact CRISPR System for In-Vivo Delivery

New NIH-backed research creates miniaturized CRISPR editors small enough for efficient viral delivery throughout the body

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Apr 12, 2026BREAKING

CRISPR Goes Cut-Free: New Gene Editor Skips DNA Breaks

Scientists develop CRISPR system that edits genes without cutting DNA, potentially solving off-target issues

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Apr 10, 2026MARKET

Goldman Raises Generate Biomedicines Target to $26

Goldman Sachs maintains Buy rating on Generate Biomedicines, lifting price target to $26 amid AI protein design momentum

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Apr 10, 2026BREAKING

Chinese CRISPR Therapy Eliminates Transfusions for Beta Thalassemia

Five patients no longer need blood transfusions after Chinese CRISPR treatment, signaling cost-competitive challenge to US therapies

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Apr 9, 2026BREAKING

Beta-Thalassemia Gene Editing Shows 95% Success in Phase 3 Trial

CTX001 gene therapy achieves transfusion independence in 95% of patients with severe beta-thalassemia

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Apr 9, 2026BREAKING

Cantor Initiates Generate Bio With Buy Rating

Cantor Fitzgerald initiates coverage of Generate Biomedicines with Buy rating, highlighting AI-driven protein design platform

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Apr 9, 2026BREAKING

Roche Backs C4's Degrader-Drug Conjugates with $20M Deal

Swiss pharma giant expands decade-long C4 partnership to develop degrader-antibody conjugates targeting undruggable proteins

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Apr 8, 2026BREAKING

Plant Molecular Farming Reaches Cost Parity with Microbial Systems

Digital manufacturing advances drive plant-based protein production to competitive cost structure versus traditional platforms

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Apr 7, 2026BREAKING

Magdalena Builds 650,000L Precision Fermentation Plant in Guatemala

Sugar producer Magdalena launches massive precision fermentation facility, marking Central America's largest synbio investment

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Apr 7, 2026BREAKING

CRISPR Startup Defeats $50B Giant in Patent Battle

David vs. Goliath patent victory reshapes CRISPR licensing landscape for next-gen gene editing platforms

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Apr 7, 2026BREAKING

CRISPR screens reveal RNA targets for cancer T cell therapy

High-content CRISPR activation screens identify synthetic lethal RNA mechanisms to boost T cell cancer killing

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