Mamad Ahangari

116 posts

Mamad Ahangari banner
Mamad Ahangari

Mamad Ahangari

@centrum_blue

PhD in statistical genetics. Scientist at @herasight. Interested in decentralized AI (τ) and late antiquity history. Opinions my own.

Florida, USA Katılım Ağustos 2025
381 Takip Edilen317 Takipçiler
Mamad Ahangari
Mamad Ahangari@centrum_blue·
@timatilos @sobczak_mariusz @theminos_ai @ConnitoAI Great idea. We’re planning to do some targeted rounds for specific diseases later in the summer, and someone else has already asked about CAG expansions for Huntington's. We could also dedicate a timeframe specifically to the COCH gene.
English
0
0
2
103
Lultimate ⭐
Lultimate ⭐@timatilos·
Why I'm all-in on @theminos_ai and will never unstake: My partner and two of my children have hereditary deafness linked to a COCH gene mutation. Research into rare genetic disorders barely gets funded. SN107 brings clinical-grade genomic variant calling on-chain. This isn't a meme. It matters. Proud to hold
English
3
0
3
122
Mariuszek
Mariuszek@sobczak_mariusz·
Today is a dump day in $TAO subnets, you can expect days like that and you need to ride them out. I haven’t sold a single alpha in @theminos_ai or @ConnitoAI , sometimes you just have to suck it in.
English
10
3
46
3.8K
Mamad Ahangari
Mamad Ahangari@centrum_blue·
@micaelabazo @rivatez If this is something you’re still looking into, I’m more than happy to put you in touch with Herasight. Just lmk.
English
0
0
0
120
Micaela
Micaela@micaelabazo·
so grateful for @rivatez research and advice. she saved me from a 'standard' molotov cocktail that would've likely come at the expense of my sanity. fertility and hormonal interventions are still wildly misunderstood and often treated as consumer products with perverse profit incentives. the first time i considered egg freezing i went to kindbody in the US. the experience was horrific. set in a mall with branded diagnostics and nuclear protocols it was impossible not to feel like i was in the wrong place. article is long and an incredible resource. recommend it to all women (and men)! still thinking about the implications of removing/reducing the competitive selection filter in birth outcomes...
Riva@rivatez

Publishing the outcome of several months of research on egg freezing and IVF, some of which shocked me. Most American women aren't told there are different versions of freezing/IVF protocols— and the version they're offered by default is often the most aggressive. In much of Europe and Japan, women get half (or less) of the same medication for the 'same' procedure and outcomes. The assumption baked into American fertility medicine is that more is better. More eggs help up to a point; past it, you're buying more hormone exposure and more risk — not necessarily more babies. Long-term safety data on healthy women taking these protocols repeatedly at these doses doesn't yet exist. The studies that look reassuring follow women for 5-10 years, not 30. Full essay linked below. I tried to write the overview I couldn't find while making these decisions.

English
2
1
35
5.8K
Mamad Ahangari retweetledi
Herasight
Herasight@herasight·
Even with one embryo, PGT-P can still be useful. You can compare it to simulated embryos from your own genetics to decide whether to transfer or attempt another round of egg retrieval. Studies measuring only expected risk reduction miss this form of "efficacy".
Alexander Craig@alex1craig

Klausner et al. makes a valuable contribution to modeling polygenic embryo screening (PES) efficacy in real-world IVF data. However, there are some important methodological and conceptual limitations worth discussing 🧵

English
2
8
18
2.6K
Mamad Ahangari retweetledi
Jonathan Sebat
Jonathan Sebat@sebatlab·
I'm pleased to share our latest preprint: Combinatorial effects of gene dosage, polygenic background and environment on complex traits 🧵medrxiv.org/content/10.648…
English
4
38
114
19.7K
Mamad Ahangari
Mamad Ahangari@centrum_blue·
We can generate Huntington’s-specific genomes and run a full benchmark focused on CAG repeat expansion calling for Huntington's in the summer. Repeat expansions and CNVs are already on our roadmap, so this is a strong real-world use case. After the run, we’ll share the variant caller pipeline with HDSA to improve their calling.
English
1
0
2
51
Vincent Cavallaro
Vincent Cavallaro@VCavs87·
Jon Cipher@_joncipher

$TAO Making a difference! ⬇️⬇️ MINOS SN 107 👀👀 Alagille syndrome is a rare genetic disorder affecting roughly 1 in 30,000–50,000 live births. It causes problems in multiple organs, especially the liver (due to missing or reduced bile ducts leading to cholestasis, severe itching, and growth issues), heart, skeleton, eyes, and blood vessels. Prognosis varies widely — overall survival is around 80–90% into adulthood, but 20–30% of patients eventually need a liver transplant, and native liver survival drops to about 40% by age 18. Current treatments focus on symptom management (e.g., medications like maralixibat or odevixibat for itching, nutritional support, and surgery), with liver transplantation as the main option for severe cases. There is no cure that fixes the underlying JAG1 mutation. Why better analysis in this region helps: Accurate, low-cost detection of JAG1 variants enables earlier diagnosis, personalized monitoring, and timely interventions — potentially reducing complications, improving quality of life, and lowering the need for costly transplants or long-term care. This is exactly where Minos’ decentralized AI validation adds real clinical value. Minos’ value mining near the JAG1 (chr20:11M-16M) region: Imagine trying to read a critical page in a book, but some words are smudged or in hard-to-read font. Traditional DNA analysis tools often struggle in this specific JAG1 region — it’s technically “noisy” and error-prone. What Minos is doing: • They’re crowdsourcing thousands of decentralized AI “miners” to double-check and perfect the reading of this exact region. • Goal: Reach near-perfect accuracy (F1 score 0.95–0.99), matching or beating top tools like DeepVariant and DRAGEN. Why this matters (the real value): • Mutations here cause Alagille syndrome — a serious condition affecting the liver, heart, bones, and more. • Better accuracy = faster, more reliable diagnoses → earlier treatment, better patient outcomes, and fewer unnecessary tests. • For researchers and clinics: Cheaper re-analysis of existing DNA data (saving $10–$100+ per sample in this region) instead of expensive re-sequencing. • Long-term: This proves decentralized AI can deliver clinical-grade genomics at lower cost, opening the door for broader, more affordable precision medicine. In short: Minos is turning a hard, high-stakes genomic “problem zone” into a reliable, low-cost strength — directly helping rare disease patients while showing how decentralized AI can compete with (or beat) big centralized tools. This small region is a perfect showcase for the whole project’s potential. #Genomics #PrecisionMedicine #AlagilleSyndrome #JAG1 #Bittensor #DeAI #BioTech #HealthTech #RareDisease #DNA $TAO

QAM
1
0
3
79
Mamad Ahangari retweetledi
PGC Consortium
PGC Consortium@PGCgenetics·
New autism GWAS incoming! At #INSAR2026, @jakob_grove presented the latest updates on the yet-to-be-released autism GWAS. Curious about the findings? Find them below ⬇️
PGC Consortium tweet media
English
2
12
53
13.3K
Mamad Ahangari
Mamad Ahangari@centrum_blue·
At my previous job, I worked with one of the largest genomics testing companies in livestock/cattle, and it’s interesting how often I see people talk about this industry like it’s just shepherds, milk, and beef with no understanding of how much optimization is already happening. Modern cattle production is built on herd management, genetic testing, breeding decisions, disease screening, and constant selection for better performance. It’s actually one of the most mature real-world applications of genetics. When people talk as if nothing has changed in 100 years and we're just dealing with cow farting, it usually means they don’t understand what they’re criticizing.
English
0
0
1
47
Mamad Ahangari
Mamad Ahangari@centrum_blue·
Exactly. That’s why SN107 put substantial time and effort with @TargonCompute to bring MinosVM live ahead of mainnet launch. Detailed docs are nice, but mining should be the easiest thing possible imo. In the case of SN107, just spin up a MinosVM on Targon and type bash start-miner.sh You can even delegate the whole thing to your agent.
English
1
1
9
219
Mamad Ahangari
Mamad Ahangari@centrum_blue·
@sobczak_mariusz nailed it. SN55 is producing synthetic genomes. SN107 is building the infra for genomics and is making pipelines and codes the commodity, not the generated outputs. Minos has an article on synthetic genomes dropping soon, hopefully later today. tl;dr: with modern GPUs and some statistical genetics knowledge, generating synthetic cohorts is becoming increasingly tractable. The harder problem (I think) is proving they are realistic, useful, and benchmarkable.
English
0
0
1
64
Mariuszek
Mariuszek@sobczak_mariusz·
Pro tip: never ever sell @theminos_ai. This is one of the most misunderstood asymmetric bets in the entire $TAO ecosystem. People look at SN107 and think “genomics narrative.” I think that is way too shallow. Minos is building at the validation layer, where raw DNA becomes trustworthy signal. Variant calling, benchmarking, synthetic genomes, known truth sets — this is the boring but critical infrastructure every serious genomics model will eventually need. And yes, that includes the frontier labs. If @OpenAI or anyone else builds serious genomics models, they are going to need mountains of validated genomes, benchmarked variant-calling pipelines, and clean datasets where the correct answer is actually known (this is a hint boys and girls). That is what makes @centrum_blue so important. He is not a crypto guy borrowing a DeSci story. He has a PhD in statistical genetics and is building directly in his domain. In genomics, you cannot fake the PhD. SN55 and SN68 are interesting. But Minos sits upstream. If the genomic data layer is wrong, everything downstream is compromised. @theminos_ai is not a DeSci play. It is the data layer every serious genomics model will eventually have to touch. That is a very different thing.
English
9
8
59
8.3K
Mamad Ahangari
Mamad Ahangari@centrum_blue·
Appreciate the post @sobczak_mariusz . You’re seeing the bigger picture. The further upstream you go in genomics, the more technical the work becomes: variant calling, truth sets, benchmarking, validation and so on. But that’s exactly where the leverage is. Downstream AI only works if the signal underneath is real. That’s why SN107 starts at this layer. Bittensor is the only place where “is this variant call correct?” can become an economic signal at scale. It’s not that genomics needs crypto. It’s that building this foundational layer needs an incentive mechanism, and Bittensor already has one... and OpenAI stepping into genomics just compresses the timeline.
English
1
2
4
198
Mamad Ahangari retweetledi
Jeremy
Jeremy@jeremyli__·
Excited to share GeneBench, a genomics eval I've developed w/ @OpenAI that measures whether current models can execute realistic end-to-end scientific analyses where good scientific judgement is required. tl;dr they’re getting close, but aren’t quite there yet
Jeremy tweet media
OpenAI@OpenAI

Introducing GPT-5.5 A new class of intelligence for real work and powering agents, built to understand complex goals, use tools, check its work, and carry more tasks through to completion. It marks a new way of getting computer work done. Now available in ChatGPT and Codex.

English
6
26
128
32K
Mamad Ahangari
Mamad Ahangari@centrum_blue·
@const_reborn We’ve already stored more than 1 TB of synthetic genomes on Hippius for @theminos_ai and we’re just getting started. This dataset will keep growing month after month. Only possible on bittensor.
Mamad Ahangari tweet media
English
5
4
36
1.8K
Mamad Ahangari retweetledi
Alex Strudwick Young
Alex Strudwick Young@AlexTISYoung·
I'll be going live on @tbpn today at around 1140 pacific to discuss the polygenic embryo testing industry and related topics. Tune in @tbpn.
English
1
12
52
3.2K
Mamad Ahangari retweetledi
William J. Greenleaf
William J. Greenleaf@WJGreenleaf·
Our Human Multiomic Development Atlas paper is out in Nature today! A heart-felt "thank you" to all co-authors for their tireless work on this complex yet exciting project! Congrats all! nature.com/articles/s4158…
English
6
99
356
22.1K
Mamad Ahangari
Mamad Ahangari@centrum_blue·
I saw this yesterday and thought it was cool. I probably would’ve loved this a year ago though. I do wonder how necessary it really is at this point. I’m working on a large batch of sumstats for a project, including PGC on Figshare that are annoying to access manually. This time, I just asked Claude Code to create a manifest for the latest PGC sumstats and download them for me.
English
2
0
6
271