山色迤逦皆因我 |心澄如镜,写皆所得|DEX researcher | 穷尽其解

Manchester, England
ALNY我是很看好的,但确实很多东西需要学的太多,导致最近交易策略研究的少了一些。 最近有了一些新的想法,在找一些PHD来合伙帮助我做一些研究,要学的实在太多,我不可能事事专精。 风物长宜放眼量。
这两天卖了ALNY,传奇生物的PUT 看的我心力憔悴。
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这两天卖了ALNY,传奇生物的PUT 看的我心力憔悴。
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快ipo了得搞个大新闻 数学题,生物题都做了,为啥不做物理题
Today we announced the Claude-led discovery of a molecular machine that we suspect could represent a new gene editing mechanism. Its precise function, biotechnological utility (if any), or level of significance is not yet clear, but at minimum it is work I would have been proud to do as a PhD student. The work was done mostly, though not entirely, by Claude: our life sciences team suggested a broad area of research, Claude read through the literature and a bunch of genome data and discovered something interesting, then Claude proposed experiments to verify the discovery and our team carried them out. It’s easy to dismiss this as a one-off or curiosity, but we’ve repeatedly seen a pattern where AI performance in new intellectual domains goes from weak to superhuman in a matter of a few years. In 2023 models struggled to do math at the level of an average high-school student. In 2024 they started to do well on math competitions for the best high-schoolers in the country, in 2025 they started to solve minor open problems, in early 2026 more significant open problems, and in late 2026 they are beginning to solve the top few open problems in all of mathematics. We believe AI for biology is on a similar exponential trend. The main difference between biology and mathematics, of course, is that math can be done purely theoretically, while biology requires experimentation. Some have used this to draw the conclusion that AI’s utility in biology will be limited. We think this is wrong. As we’ve demonstrated today, humans can collaborate with AI to perform the experiments, validate key results in a few weeks and, if necessary, work with the AI to iterate on what they find. Eventually it may even be possible for Claude itself to safely perform the experiments by autonomously controlling lab equipment, with appropriate safeguards in place, but we aren’t doing that today (our lab is also a BSL1/BSL2 facility that doesn't handle materials dangerous to humans). More broadly, biomedical advancement has many stages — from fundamental biology discoveries, to translational research, to drug discovery, clinical trials, and finally the actual delivery of medicines and health care to patients. We are also interested in these later stages, but even simply accelerating the first stage of fundamental biological discoveries has the potential to speed up and broaden the entire pipeline. Improving our understanding of biology and sharpening biologists’ tools can drive forward all of the later stages, for example by identifying new drug targets, finding new therapeutic modalities, allowing for more precise measurement, and speeding up the experimental loop which itself further accelerates our understanding of biology. This will not in itself speed up clinical trial times, but if it succeeds it could greatly increase the number of promising candidates that go into the pipeline — an increase in throughput even though latency remains. In Machines of Loving Grace, I wrote about AI’s potential to “cure most diseases in 5-10 years” — a goal that sounds impossible, but one I believe is just barely possible if AI is applied to every stage of the pipeline. The first step is showing that AI can first help with, and then drive, biological discoveries. Claude’s discovery is the latest in a line of related prior work that goes back decades, beginning with systems like CRISPR, and continuing with discoveries like the bridge recombinase and VIPR in the past few years. Recently, there has been heightened interest in systems based on reverse transcriptase (RT) enzymes, the enzyme underlying the system Claude identified. And most recently, a Stanford team working independently described a novel RT system with an associated non-coding array that is in some ways similar to the one Claude found, though they are distinct systems that evolved independently from each other. I believe that we’re at the very beginning of finding such systems and developing them into powerful tools for biotechnology. I’m proud of the resources Anthropic has invested in accelerating the public benefits of AI through the life sciences, and we’re aiming both to grow our life sciences team and to work with other scientists to extend this approach to a broad range of problems. If you have a proposal for a research collaboration or are interested in joining our life sciences team, please reach out.
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You need to learn“摸奶来财”
中文感觉是需要学学了
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这个是毋庸置疑的 看接下来几个季度财报端是否带来增量订单。
Is AI actually speeding up drug discovery? According to new McKinsey research, there are early signs that it is: all of these candidates were AI-enabled, with discovery time cut by ~15-80%. (Incredibly bullish)
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如果你开始相信
艾德生物挺好的,市场的顾虑是老板太老,代际传承怎么处理。 但实际上这个价格是偏低的,公司基本面没有任何问题,国药集团溢价购买,渠道应该还会放量。 在精准医疗叠加ai的大浪潮下持续看好。
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RT @mdzzi: @_wmoon 因为我有一颗无比坚信AI能改变当前制药和诊断的信心。 所以现在我把大部分的仓位和时间逐帧去研究我手里的每一个标的。 我喜欢赔率高,充满冒险的,没有回头路的赛道。管线就是人类冒险者的游戏,要么赢,要么输。
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SDGR确定性的三支箭: 第一支:2027 年第一季度FDA 对 Zasocitinib(TAK-279)做出最终上市批准裁决,若正式获批,这将是全球首款完全由计算机第一性原理/物理模拟辅助设计诞生的重磅商业化新药。获批将直接触发武田 20 亿美元里程碑池中的监管批准分红款项流向薛定谔,并开启 2027 年上半年商业化销售后的全球销售里程碑与特许权提成。 第二支:自研临床管线对外授权,作为全资自研的先导小分子,SGR-1505 已获得 FDA 授予的快速通道和孤儿药资格,且在华氏巨球蛋白血症(WM)等耐药 B 细胞淋巴瘤中展现了突破性单药活性。公司正在完成其临床 I 期的完整数据包。 其中管理层已明确表态将在完成 I 期后将其商业化权利整体对外授权转让。市场正密切盯防其与跨国制药巨头(MNC)签署独家授权协议的落地,潜在的大额不可退还预付款。 第三支:Bunsen 智能体平台全面铺开与计算毒理学商业化。继百时美施贵宝之后,观察是否有第二家跨国制药巨头宣布全公司规模化采购 Bunsen平台。其中公司指引在 2026 年内完成 50 余个核心抗靶标毒理学模拟的客户测试并正式商业化,这有望直接为下半年的软件合同客单价带来增量。 当前价格反应的是第一支箭,带来的涨幅,我认为今年还有两支箭没有落地,拭目以待。
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最近老有人微信私我,问卖飞HYPE,LIT,BP,PURR怎么看。 我能怎么看?我想说的是我认知水平只允许我持有这么久,我看到的是每一次我都能赶上,从一个辍学为生计犯愁的学生,到现在可以放松体验人生的跃迁。 我明白自己耐以生存的技巧从来不是老鼠仓,不是做项目,不是讨好他人,不是跟单。而是属于我的第一性原理:靠脑子吃饭,靠认知赚钱。
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艾德生物挺好的,市场的顾虑是老板太老,代际传承怎么处理。 但实际上这个价格是偏低的,公司基本面没有任何问题,国药集团溢价购买,渠道应该还会放量。 在精准医疗叠加ai的大浪潮下持续看好。
不是一个东西,买艾德是因为市场更多顾虑的是管理层换代的事 英矽智能太贵了,需要兑现的东西太多了,稍有不慎就是暴跌。
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做减法。
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三根大阳线,打爆所有偏见。
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在被某只消费股给打坠机后 我的账户今年第一次超过一月,迎来新高。 感谢TEMPUS SDGR
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SDGR,真正要看的是 Bunsen。管理层说这是公司近 20 年新产品里客户兴趣最强的一档,抢的是药企新增 AI/自动化预算,不是侵占自己家旧软件业务,其中BMS 已经大规模部署。 9月14日 Mo­r­g­an St­a­n­l­ey He­a­l­t­h­c­a­re Co­n­f­e­r­e­n­ce 的管理层交流出现了几个能改变软件业务估值预期的信息:软件 ACV 同比增长27%;Ho­s­t­ed So­f­t­w­a­re 占比已经达到 47%,云迁移速度快于原计划。 SDGR现在的涨幅是前菜,还有管线的历史包裹,以及bunsen年底业绩的第一考。(大摩原文放评论区。)
Sdgr这几天涨也不是瞎涨。 Za­s­o­c­i­t­i­n­ib(TAK-279,扎索替尼,原NDI-034858)武田NDA了。 目前AI制药唯一通过三期的药物,由SD­GR薛定谔FEP+自由能微扰AI分子模拟,计算筛选得到分子。希望你懂我意思
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我是纯粹的社交孤儿。 币圈数得上来深交的朋友就那么一两个,我更多的朋友是爬山,无畏契约,打网球,以及读书时代的朋友。(值得一提的是在这期间认识了一位屠宰场朋友,深夜杀完牛和我一起打瓦真是快哉快哉) 掺杂了利益之后,似乎感情总是有那么些杂质,我只能钟情山水,活在方圆之内。
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Sdgr这几天涨也不是瞎涨。 Za­s­o­c­i­t­i­n­ib(TAK-279,扎索替尼,原NDI-034858)武田NDA了。 目前AI制药唯一通过三期的药物,由SD­GR薛定谔FEP+自由能微扰AI分子模拟,计算筛选得到分子。希望你懂我意思
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雨崩已经走了两天。 香格里拉的滴滴师傅跟我聊《消失的地平线》,聊詹姆斯希尔顿从来没有到过中国。我很惊诧,师傅懂这么多。 下雨,天气不是很好,神山隐翳,突然把康伟见到的秘境带入到这十分相似。 想过很多问题,也想写很多东西,答案没有头绪,写出来也反复删改。 留给我的是路上沉重的呼吸。
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在某个角落签下我对人生的注解:山色迤逦皆因我。
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