AI can now write genomes from scratch.
Arc Institute an NVIDIA just published Evo-2, the largest AI model for biology, trained on 9.3 trillion DNA base pairs spanning the entire tree of life.
it doesn’t just analyze genomes. it creates them 1/
Evo 2 generates mitochondrial, prokaryotic, and eukaryotic sequences at genome-scale
Evo 2 is FULLY OPEN, including model parameters, training code, inference code, and
the OpenGenome2 dataset LMFAO
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think of it as a DNA-focused LLM. instead of text, it generates genomic sequences. it reads and interprets complex DNA, including noncoding regions usually considered jink, generates entire chromosomes and new genomes, and predicts disease-causing mutations, even those not understood
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this is biology hacking
AI is moving beyond describing biology to designing it. this allows for synthetic life engineered from scratch, programmable genomes optimized by AI, potential new gene therapies, and lays the groundwork for whole-cell simulation.
biology is becoming a computational discipline
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it was trained on a dataset of 9.3 trillion base pairs from bacteria, archaea, eukaryotes, and bacteriophages
it processes up to 1 million base pairs in a single context window, covering entire chromosomes. it identifies evolutionary patterns previously unseen by humans
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Evo-2 has demonstrated practical generation abilities, creating synthetic yeast chromosomes, mitochondrial genomes, and minimal bacterial genomes.
this is computational design in action.
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Evo-2 understands noncoding DNA, which regulates gene expression and is involved in many genetic diseases.
it predicts the functional impact of mutations in these regions, achieving state-of-the-art performance on noncoding variant pathogenicity and BRCA1 variant classification.
this could lead to advances in precision medicine
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Evo-2 uses stripedhyena 2, combining convolution and attention mechanisms, not transformers.
it models DNA at multiple scales, capturing long-range interactions, and autonomously learns features like exon-intron boundaries and transcription factor binding sites without human guidance.
it’s not just memorizing
it’s understanding biology.
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Evo-2 predicts whether mutations are harmful or benign without specific training on human disease data.
WHAT
it outperforms specialized models on BRCA1 variants and handles noncoding mutations effectively, suggesting it has learned DNA’s fundamental principles
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Evo-2 generates DNA sequences that influence chromatin accessibility, controlling gene expression.
it has embedded simple Morse code into epigenomic designs as a proof of concept, not a practical application. this shows potential for designing programmable gene circuits.
make me blonde. thank you
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Evo-2 is FULLY OPEN SOURCE, including model parameters, training data, and code.
this will lead to massive widespread innovation in bioengineering, lowering barriers to genome design.
it’s a revolution moment for the field.
the era of biotech is here
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The Arc Institute aims to model entire cells, moving beyond DNA to whole organisms.
this could lead to AI creating new life forms and synthetic biology becoming AI-driven.
the future involves programming life at increasing scales
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three years ago, AI focused on chatbots.
now it generates genomes. soon, it will design complex biological systems. this is a new phase
humans are no longer just studying biology but rewriting its code.
biology’s future is computational. are you prepared?
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it’s low because modern life is designed against your biology and no one taught you how to rebuild from scratch.
here’s the 9-layer protocol to restore your hormonal health 1/
a new study out of Japan just showed how much behavior is linked to genetics
basically showing that fear, boldness, and social tendencies are rooted in your DNA
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this is the most comprehensive behavioral-genetic dataset ever created in Drosophila melanogaster (fruit flies)
36,600 flies
105 distinct genotypes
standardized threat simulations
single and group contexts
result:
→ behavior is not random
→ behavior is heritable
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in identical environments, genetically distinct flies responded differently to the same threat.
some froze. others explored. some clustered tightly. others drifted alone.
the key variable wasn’t trauma, mood, or social learning.
it was genotype.
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your body didn’t evolve for blue light, seed oils, comfort, or porn
it evolved to fight, fuck, sleep well, and struggle
modern life destroys your hormones
here’s how to take them back 1/
your hormones are the operating system of your body.
modern life is the malware.
here's why
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hormones are chemical messengers that control literally everything: your energy, mood, muscle, fertility, sleep, and even your status compared to others
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chronic cardio lovers are endurance-obsessed martyrs
but their mitochondria know the truth: resistance training gives you superior metabolic adaptations with lower inflammatory cost
the weight room leads to metabolic advantages that traditional cardio cannot match
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mechanism: resistance training stimulates all three major muscle fiber types, while steady-state cardio primarily involves slow-twitch fibers
limiting the stimulus to one fiber type creates metabolic imbalance. full spectrum recruitment optimizes mitochondrial adaptation
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new brain-computer interface so small it slips between your hair follicles just solved the last barrier to neural control: movement
96.4% accuracy while running.
this means AR glasses you control with thought, anywhere, anytime 1/
non-invasive brain-computer interfaces have a huge problem: motion artifacts corrupt signals during movement. wet electrodes need gel, dry ones require pressure, and both fail during activity.
the result is that BCIs are basically useless in the real world 2/
these micro-brain sensors are tiny cross-shaped needles with conductive polymer coatings that target gaps between hair follicles. they penetrate just the outer skin layers, bypassing the insulating stratum corneum to establish direct contact with brain signals 3/
your cells are continuously monitoring your physical activity. sedentary behavior triggers an immediate metabolic revolt. barely a week of inactivity spikes insulin resistance by 29%. no opinions, just biochemistry
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muscle tissue is responsible for 80% of post-meal glucose consumption. sedentary muscles refuse this task, forcing pancreatic exhaustion. your insulin screams into deaf cellular ears.
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