We shared this request example with FAB participants: url_qparams = { "limit": count, "offset": offset, "has_group": "false", "order_by": "-activity", "forecast_type": "binary", "project": tournament_id, "status": "open", "type": "forecast", "include_description": "true", } url = f"{api_info.base_url}/questions/" response = requests.get( url, headers={"Authorization": f"Token {api_info.token}"}, params=url_qparams )

But we don't want to support all these parameters, and the ones relevant are: - order_by - status - project - forecast_type - we ignore this, but assume it's binary - FAB only supports binary for now.

GET /api2/questions/?format=api&offset=3020
HTTP 200 OK
Allow: OPTIONS, GET
Content-Type: application/json
Vary: Accept

{
    "count": 5975,
    "next": "http://www.metaculus.com/api2/questions/?format=api&limit=20&offset=3040",
    "previous": "http://www.metaculus.com/api2/questions/?format=api&limit=20&offset=3000",
    "results": [
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                "title": "Will top institutions participating in the UK’s global AI Safety Summit make concrete and meaningful commitments to advance AI safety?",
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                "description": "*This question was written in partnership with the [Effective Institutions Project](https://effectiveinstitutionsproject.org/).*\n\nThe [UK AI Safety Summit](https://www.gov.uk/government/publications/ai-safety-summit-introduction/ai-safety-summit-introduction-html) is taking place November 1st and 2nd, 2023. [According to Computerworld](https://www.computerworld.com/article/3706051/uk-government-outlines-five-objectives-for-ai-safety-summit.html):\n\n> The five objectives of the UK government’s summit are:\n> \n> - Develop a shared understanding of the risks posed by frontier AI and the need for action\n> - Put forward process for international collaboration on frontier AI safety, including how best to support national and international frameworks\n> - Propose appropriate measures which individual organisations should take to increase frontier AI safety\n> - Identify areas for potential collaboration on AI safety research, including evaluating model capabilities and the development of new standards to support governance\n> - Showcase how ensuring the safe development of AI will enable AI to be used for good globally.\n\nArguably a large part of whether the summit is successful lies in whether or not leading AI labs, and the governments that regulate them, make commitments that they would not have made had the summit not been convened.",
                "resolution_criteria": "The question resolves **Yes** if the UK AI Safety Summit results in a joint declaration or statement, endorsed by at least five of the top institutions cited in Effective Institutions Project’s [AI governance primer](https://effectiveinstitutionsproject.substack.com/i/135267188/the-top-institutions-for-ai-governance) who are also participating parties (nations and/or labs) in the Summit, that includes at least three of the following commitments [proposed by the Future of Life Institute](https://futureoflife.org/wp-content/uploads/2023/09/FLI_AI_Summit_Recommendations.pdf):\n\n* An agreement to reconvene in six months (or less) to work on AI governance\n* A commitment to increase public funding for AI safety research\n* A commitment by signatory nations to develop a national-level AI strategy that contains at least two of the following measures:\n    * Standards for advanced AI, with associated benchmarks and thresholds for dangerous capabilities\n    * Mandatory pre-deployment audits for potentially dangerous AI systems by independent third parties\n    * Monitoring of entities with large-scale AI compute concentrations\n    * Safety protocols to prevent systems with dangerous capabilities from being developed, deployed, or stolen\n    * Restrictions on open source AI based on capability thresholds\n    * Immediate enhancement of cybersecurity standards at leading AI companies\n    * Adaptation of national liability law to AI-specific challenges\n* A post-summit working group with a mandate to develop a blueprint for international AI governance\n* Encouragement of AI labs to share information with the UK Foundation Model Task Force\n\nThe question also resolves **Yes** if no such declaration is issued, but the [Future of Life Institute](https://futureoflife.org/) issues a public statement indicating that the outcomes from the summit have nevertheless exceeded the organization’s expectations.",
                "fine_print": "* A joint declaration or statement endorsed by at least five of the following institutions or official representatives of the institutions attending the Summit is required for resolution:\n\n    * The United States government\n    * The Chinese government\n    * The European Union\n    * OpenAI\n    * Google DeepMind\n    * Anthropic\n    * Alphabet\n    * Microsoft\n    * Amazon\n    * Meta\n\n* A joint statement meeting these criteria must be publicly available before November 10, 2023, or 168 hours following the end of the Summit, whichever is later.\n\n* If the UK AI Summit does not take place before March 1, 2024, this question will resolve as **No**.",
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                "title": "Will the EU AI Act implement regulations on foundation models?",
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                "description": "*This question was written in partnership with the [Effective Institutions Project](https://effectiveinstitutionsproject.org/).*\n\nThe final version of the [EU AI Act](https://artificialintelligenceact.eu/the-act/) is currently being negotiated. This act aims to place significant regulation on the development and use of AI. The proposed language establishes [four levels of risk from AI systems](https://digital-strategy.ec.europa.eu/en/policies/regulatory-framework-ai): minimal, limited, high, and unacceptable. AIs classified as “unacceptable” would be outright prohibited, while the other risk categories would be subject to graduated levels of regulation.\n\nThe AI Act was [originally proposed by the European Commission (EC) in April of 2021](https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:52021PC0206). In December of 2022, the [Council of the European Union](https://en.wikipedia.org/wiki/Council_of_the_European_Union) (the Council) adopted [its “general approach”](https://artificialintelligenceact.eu/wp-content/uploads/2022/12/AIA-%E2%80%93-CZ-%E2%80%93-General-Approach-25-Nov-22.pdf), modifying the Commission’s proposed act to reflect its own position. In June of 2023, the European Parliament (EP) [adopted amendments](https://www.europarl.europa.eu/doceo/document/TA-9-2023-0236_EN.html) to the Commission’s draft, staking its own position. The next stage is known as a “[trilogue](https://eur-lex.europa.eu/EN/legal-content/glossary/trilogue.html)” between the three bodies to reach a provisional agreement on the final text. The Future of Life Institute (FLI) maintains a website with detailed information regarding the AI Act: see [this page](https://artificialintelligenceact.eu/context/) for context and timelines and [this page](https://artificialintelligenceact.eu/documents/) for links to relevant documents.\n\nNotably, the the Council's version would set forth regulations on general-purpose AI (GPAI) systems, such as OpenAI's ChatGPT. The EP’s version would also impose requirements on systems like ChatGPT, which it describes as “foundation models”, and defines as follows:\n\n>‘foundation model’ means an AI system model that is trained on broad data at scale, is designed for generality of output, and can be adapted to a wide range of distinctive tasks;\n\nThe proposed language from the **the Council** does not automatically classify GPAIs as high risk, but does subject GPAIs to a form of the regulations imposed on high risk AI (the implementation of these regulations is to be specified in [implementing acts](https://www.consilium.europa.eu/en/council-eu/decision-making/implementing-and-delegated-acts/#:~:text=An%20implementing%20act%20is%20a%20non%2Dlegislative%20act%20laying%20down%20detailed%20rules%20allowing%20the%20uniform%20implementation%20of%20legally%20binding%20Union%20acts.) adopted after the AI Act enters into force), only allowing an exemption “when the provider has explicitly excluded all high-risk uses in the instructions of use or information accompanying the general purpose AI system”. The regulations would include implementing a risk management system, data governance and management requirements, event logging capabilities, and more. For more detail see Title IA of the the Council's [proposed act](https://artificialintelligenceact.eu/wp-content/uploads/2022/12/AIA-%E2%80%93-CZ-%E2%80%93-General-Approach-25-Nov-22.pdf).\n\nThe **EP**’s amendments would similarly not automatically classify foundation models as high risk, but would impose specific requirements on foundation models. The requirements include identifying, reducing, and mitigating “reasonably foreseeable risks to health, safety, fundamental rights, the environment and democracy and the rule of law” during model development, data governance measures, and more. Specifically for generative AI, the proposed text would also require that the model provider implements means to inform the end user that they are interacting with an AI, implement safeguards against generating content that would violate EU law, and make public a “sufficiently detailed summary” of copyrighted training data used in the model. For more detail see Article 28 b of the EP’s [proposed amendments](https://www.europarl.europa.eu/doceo/document/TA-9-2023-0236_EN.html).\n\nIf interested, see the [World Economic Forum's explainer](https://www.weforum.org/agenda/2023/06/european-union-ai-act-explained/) for more detail and background on the act.\n\nSee also our question \"[When will the EU pass the AI Act?](https://www.metaculus.com/questions/8787/passing-of-the-ai-act/)\".",
                "resolution_criteria": "This question resolves as **Yes** if the final version of the EU AI Act includes requirements on providers of foundation models, as outlined in the European Parliament’s negotiating mandate for the Act in [Article 28b](https://www.europarl.europa.eu/doceo/document/TA-9-2023-0236_EN.html#:~:text=28%20b%20(new)-,Article%2028%20b,-Obligations%20of%20the). Any of the requirements in parts a through g of paragraph 2 and parts a through c in paragraph 4 of Article 28b qualify for the purposes of this question.",
                "fine_print": "* The inclusion of any of the regulations related to foundation models in parts a through g of paragraph 2 and parts a through c in paragraph 4 of Article 28b is sufficient for a **Yes** resolution:\n\n> 1. A provider of a foundation model shall, prior to making it available on the market or putting it into service, ensure that it is compliant with the requirements set out in this Article, regardless of whether it is provided as a standalone model or embedded in an AI system or a product, or provided under free and open source licenses, as a service, as well as other distribution channels. \n\n> 2. For the purpose of paragraph 1, the provider of a foundation model shall: \n\n> (a) demonstrate through appropriate design, testing and analysis the identification, the reduction and mitigation of reasonably foreseeable risks to health, safety, fundamental rights, the environment and democracy and the rule of law prior and throughout development with appropriate methods such as with the involvement of independent experts, as well as the documentation of remaining non-mitigable risks after development \n\n> (b) process and incorporate only datasets that are subject to appropriate data governance measures for foundation models, in particular measures to examine the suitability of the data sources and possible biases and appropriate mitigation \n\n> (c) design and develop the foundation model in order to achieve throughout its lifecycle appropriate levels of performance, predictability, interpretability, corrigibility, safety and cybersecurity assessed through appropriate methods such as model evaluation with the involvement of independent experts, documented analysis, and extensive testing during conceptualisation, design, and development; \n\n>(d) design and develop the foundation model, making use of applicable standards to reduce energy use, resource use and waste, as well as to increase energy efficiency, and the overall efficiency of the system, without prejudice to relevant existing Union and national law. This obligation shall not apply before the standards referred to in Article 40 are published. Foundation models shall be designed with capabilities enabling the measurement and logging of the consumption of energy and resources, and, where technically feasible, other environmental impact the deployment and use of the systems may have over their entire lifecycle; \n\n> (e) draw up extensive technical documentation and intelligible instructions for use, in order to enable the downstream providers to comply with their obligations pursuant to Articles 16 and 28(1);. \n\n> (f) establish a quality management system to ensure and document compliance with this Article, with the possibility to experiment in fulfilling this requirement, \n\n> (g) register that foundation model in the EU database referred to in Article 60, in accordance with the instructions outlined in Annex VIII point C. \n\n> When fulfilling those requirements, the generally acknowledged state of the art shall be taken into account, including as reflected in relevant harmonised standards or common specifications, as well as the latest assessment and measurement methods, reflected in particular in benchmarking guidance and capabilities referred to in Article 58a; \n\n> 3. Providers of foundation models shall, for a period ending 10 years after their foundation models have been placed on the market or put into service, keep the technical documentation referred to in paragraph 2(e) at the disposal of the national competent authorities \n\n> 4. Providers of foundation models used in AI systems specifically intended to generate, with varying levels of autonomy, content such as complex text, images, audio, or video (“generative AI”) and providers who specialise a foundation model into a generative AI system, shall in addition \n\n> a) comply with the transparency obligations outlined in Article 52 (1), \n\n> b) train, and where applicable, design and develop the foundation model in such a way as to ensure adequate safeguards against the generation of content in breach of Union law in line with the generally-acknowledged state of the art, and without prejudice to fundamental rights, including the freedom of expression, \n\n> c) without prejudice to Union or national or Union legislation on copyright, document and make publicly available a sufficiently detailed summary of the use of training data protected under copyright law. \n\n* If changes in wording to the EU Parliament negotiating mandate are made through the European AI Act Trilogues, but the substance of any of the above restrictions is incorporated into the final version of the Act, the question may still resolve **Yes** at the discretion of Metaculus.\n\n* Similarly, if the term “foundational models” is replaced with a different term (for example, general-purpose AI), but the substance of the regulations would still apply to models characterized as “foundational models” by the EU Parliament’s negotiating mandate, the question may also resolve **Yes** at the discretion of Metaculus. Per the text of the negotiating mandate:\n\n>‘foundation model’ means an AI system model that is trained on broad data at scale, is designed for generality of output, and can be adapted to a wide range of distinctive tasks.\n\n* If the EU's AI Act is not enacted before July 1, 2027, this question will resolve as **No**.",
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                "title": "Will the MONUSCO UN peacekeeping mission to the Democratic Republic of the Congo be extended with a military personnel ceiling above 11,000 before January 1, 2024?",
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            "description": "Since 1999, the [United Nations Organization Stabilization Mission in the Democratic Republic of the Congo](https://en.wikipedia.org/wiki/MONUSCO) (MONUSCO) has been active in the Democratic Republic of the Congo (DRC) to aid in stabilizing the region during and after the [Second Congo War](https://en.wikipedia.org/wiki/Second_Congo_War). The original mission was known as the United Nations Organization Mission in Democratic Republic of the Congo (MONUC) until 2010 when it was replaced by MONUSCO. [According to the UN](https://monusco.unmissions.org/en/about):\n\n>The new mission has been authorized to use all necessary means to carry out its mandate relating, among other things, to the protection of civilians, humanitarian personnel and human rights defenders under imminent threat of physical violence and to support the Government of the DRC in its stabilization and peace consolidation efforts.\n\nMONUSCO has been [planning for a withdrawal](https://press.un.org/en/2020/sc14374.doc.htm) from the DRC, however in September of 2023 DRC President Felix-Antoine Tshisekedi [insisted](https://apnews.com/article/congo-peacekeeping-united-nations-85bbfdfa87553d876800dfbdfd6be9b5) that the start of MONUSCO's \"accelerated retreat\" should begin a year sooner, at the end of December 2023. Following Tshisekedi's statement, the UN Security Council \"[expressed its readiness to decide](https://press.un.org/en/2023/sc15443.doc.htm), by the end of this year and as a matter of priority, the future of MONUSCO and its gradual, responsible and sustainable withdrawal, as well as realistic and concrete steps to be taken in that regard.\"\n\nThe UN had [extended the MONUSCO mandate for one year](https://press.un.org/en/2022/sc15152.doc.htm) on December 20, 2022, authorizing a troop ceiling [as follows](https://monusco.unmissions.org/sites/default/files/resolution_2666_2022_0.pdf):\n\n>. . . MONUSCO’s authorised troop ceiling will comprise 13,500\nmilitary personnel, 660 military observers and staff officers, 591 police personnel, and 1,410 personnel of formed police units, and *invites* the Secretariat to consider further reduction of MONUSCO’s level of military deployment, in line with the joint strategy on the progressive and phased drawdown of MONUSCO ([S/2020/1041](https://documents-dds-ny.un.org/doc/UNDOC/GEN/N20/287/47/PDF/N2028747.pdf?OpenElement)).\n\nAn August 2023 Report of the Secretary-General](https://reliefweb.int/report/democratic-republic-congo/options-adapting-configuration-monusco-and-future-united-nations-configuration-country-beyond-current-mandate-mission-report-secretary-general-s2023574-enarruzh) described options for the future of the mission and included the following paragraph:\n\n>As a first step towards the Mission’s full withdrawal, the force would consolidate its presence in the 13 high-risk territories of Ituri, as well as North and South Kivu. This would be accompanied by a rationalization of permanent and temporary bases that would allow the force to reduce its reliance on framework battalions in favour of units that are more fit for purpose in the current context. All units from South Kivu (southern sector) would subsequently be repatriated together with one static framework battalion from North Kivu (central sector) and some specialist units, military observers and staff officers, resulting in a reduction of its current deployed strength from 12,500 to approximately 10,500 military personnel. As the Mission’s focus shifts to North Kivu and Ituri, it would nonetheless retain projection capacity for South Kivu. The generation of heavy artillery and attack helicopters to enable MONUSCO to support FARDC and maintain a credible posture vis-à-vis armed groups, both foreign and Congolese, would remain a priority."
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                "description": "On October 2, 2023, Representative Matt Gaetz [filed a motion to vacate the Office of Speaker of the House of Representatives](https://apnews.com/article/kevin-mccarthy-matt-gaetz-speaker-vacate-congress-e7e5ccc6cf79ccbf5b4a7b73b9d5a3ae) in a bid to oust Kevin McCarthy. The resolution requires a simple majority to pass, and upon passing Kevin McCarthy would be removed from his position. Republicans [hold 221 seats in the House](https://en.wikipedia.org/wiki/United_States_House_of_Representatives) and Democrats hold 212. Assuming all Democrats vote to remove McCarthy, five Republicans would have to vote in favor of the motion to vacate as well for it to pass. According to reporter Jake Sherman, [Matt Gaetz may have the votes against McCarthy](https://twitter.com/JakeSherman/status/1709209301611409498). Sherman [also reports](https://twitter.com/JakeSherman/status/1709200194967904314) that the vote is currently scheduled for 1 PM ET on October 3, 2023.\n\nAccording to [reporting from CNN](https://www.cnn.com/2023/10/03/politics/mccarthy-gaetz-vote-motion-to-vacate/index.html):\n\n>A vote on a resolution to remove the speaker could still be preempted, however, even once it is on track to come to the floor for consideration.\n>\n>For example, when the resolution is called up on the floor, a motion to table – or kill – the resolution could be offered and would be voted on first. That vote would also only require a simple majority to succeed – and if it did succeed then there would not be a vote directly on the resolution to remove the speaker because the resolution would instead be tabled.\n\n*See below for additional background regarding the motion to vacate from [this question](https://www.metaculus.com/questions/18854/gop-calls-speaker-vote-before-october/)*\n\n---\n\n[Kevin McCarthy](https://en.wikipedia.org/wiki/Kevin_McCarthy) was elected Speaker of the US House of Representatives [on January 7, 2023](https://en.wikipedia.org/wiki/2023_Speaker_of_the_United_States_House_of_Representatives_election), after [15 ballots](https://www.metaculus.com/questions/14379/-ballot-rounds-to-elect-us-house-speaker/), the first time since 1923 an election for Speaker required more than one ballot. The contentious election and [concessions to the House Freedom Caucus](https://www.brookings.edu/blog/fixgov/2023/01/10/mccarthy-paid-a-steep-price-for-his-speakership-now-what/) — including rules that allow any member of the House to [call for a vote](https://www.nbcnews.com/politics/congress/speaker-of-the-house-ousted-motion-to-vacate-rcna64902) that would oust the Speaker by simple majority — have weakened his position as Speaker.\n\nThe rules for the House of Representatives of the 118th Congress adopt [those of the 117th Congress](https://www.govinfo.gov/content/pkg/GPO-CLERK-RULE-PAMPHLET-117/xml/GPO-CLERK-RULE-PAMPHLET-117.xml) with some amendments. The relevant portion of the rules is Rule IX, the text of which is quoted below. The [amended rules](https://www.congress.gov/bill/118th-congress/house-resolution/5/text) remove subparagraph (3) of clause 2(a) (shown in bold).\n\n>1\\. Questions of privilege shall be, first, those affecting the rights of the House collectively, its safety, dignity, and the integrity of its proceedings; and second, those affecting the rights, reputation, and conduct of Members, Delegates, or the Resident Commissioner, individually, in their representative capacity only.\n>\n>2\\. (a)(1) A resolution reported as a question of the privileges of the House, or offered from the floor by the Majority Leader or the Minority Leader as a question of the privileges of the House, or offered as privileged under clause 1, section 7, article I of the Constitution, shall have precedence of all other questions except motions to adjourn. A resolution offered from the floor by a Member, Delegate, or Resident Commissioner other than the Majority Leader or the Minority Leader as a question of the privileges of the House shall have precedence of all other questions except motions to adjourn only at a time or place, designated by the Speaker, in the legislative schedule within two legislative days after the day on which the proponent announces to the House an intention to offer the resolution and the form of the resolution. Oral announcement of the form of the resolution may be dispensed with by unanimous consent.\n>\n>(2) The time allotted for debate on a resolution offered from the floor as a question of the privileges of the House shall be equally divided between (A) the proponent of the resolution, and (B) the Majority Leader, the Minority Leader, or a designee, as determined by the Speaker.\n>\n>**(3) A resolution causing a vacancy in the Office of Speaker shall not be privileged except if offered by direction of a party caucus or conference.**\n>\n>(b) A question of personal privilege shall have precedence of all other questions except motions to adjourn.",
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            "description": "On October 2, 2023, Representative Matt Gaetz [filed a motion to vacate the Office of Speaker of the House of Representatives](https://apnews.com/article/kevin-mccarthy-matt-gaetz-speaker-vacate-congress-e7e5ccc6cf79ccbf5b4a7b73b9d5a3ae) in a bid to oust Kevin McCarthy. The resolution requires a simple majority to pass, and upon passing Kevin McCarthy would be removed from his position. Republicans [hold 221 seats in the House](https://en.wikipedia.org/wiki/United_States_House_of_Representatives) and Democrats hold 212. Assuming all Democrats vote to remove McCarthy, five Republicans would have to vote in favor of the motion to vacate as well for it to pass. According to reporter Jake Sherman, [Matt Gaetz may have the votes against McCarthy](https://twitter.com/JakeSherman/status/1709209301611409498). Sherman [also reports](https://twitter.com/JakeSherman/status/1709200194967904314) that the vote is currently scheduled for 1 PM ET on October 3, 2023.\n\nAccording to [reporting from CNN](https://www.cnn.com/2023/10/03/politics/mccarthy-gaetz-vote-motion-to-vacate/index.html):\n\n>A vote on a resolution to remove the speaker could still be preempted, however, even once it is on track to come to the floor for consideration.\n>\n>For example, when the resolution is called up on the floor, a motion to table – or kill – the resolution could be offered and would be voted on first. That vote would also only require a simple majority to succeed – and if it did succeed then there would not be a vote directly on the resolution to remove the speaker because the resolution would instead be tabled.\n\n*See below for additional background regarding the motion to vacate from [this question](https://www.metaculus.com/questions/18854/gop-calls-speaker-vote-before-october/)*\n\n---\n\n[Kevin McCarthy](https://en.wikipedia.org/wiki/Kevin_McCarthy) was elected Speaker of the US House of Representatives [on January 7, 2023](https://en.wikipedia.org/wiki/2023_Speaker_of_the_United_States_House_of_Representatives_election), after [15 ballots](https://www.metaculus.com/questions/14379/-ballot-rounds-to-elect-us-house-speaker/), the first time since 1923 an election for Speaker required more than one ballot. The contentious election and [concessions to the House Freedom Caucus](https://www.brookings.edu/blog/fixgov/2023/01/10/mccarthy-paid-a-steep-price-for-his-speakership-now-what/) — including rules that allow any member of the House to [call for a vote](https://www.nbcnews.com/politics/congress/speaker-of-the-house-ousted-motion-to-vacate-rcna64902) that would oust the Speaker by simple majority — have weakened his position as Speaker.\n\nThe rules for the House of Representatives of the 118th Congress adopt [those of the 117th Congress](https://www.govinfo.gov/content/pkg/GPO-CLERK-RULE-PAMPHLET-117/xml/GPO-CLERK-RULE-PAMPHLET-117.xml) with some amendments. The relevant portion of the rules is Rule IX, the text of which is quoted below. The [amended rules](https://www.congress.gov/bill/118th-congress/house-resolution/5/text) remove subparagraph (3) of clause 2(a) (shown in bold).\n\n>1\\. Questions of privilege shall be, first, those affecting the rights of the House collectively, its safety, dignity, and the integrity of its proceedings; and second, those affecting the rights, reputation, and conduct of Members, Delegates, or the Resident Commissioner, individually, in their representative capacity only.\n>\n>2\\. (a)(1) A resolution reported as a question of the privileges of the House, or offered from the floor by the Majority Leader or the Minority Leader as a question of the privileges of the House, or offered as privileged under clause 1, section 7, article I of the Constitution, shall have precedence of all other questions except motions to adjourn. A resolution offered from the floor by a Member, Delegate, or Resident Commissioner other than the Majority Leader or the Minority Leader as a question of the privileges of the House shall have precedence of all other questions except motions to adjourn only at a time or place, designated by the Speaker, in the legislative schedule within two legislative days after the day on which the proponent announces to the House an intention to offer the resolution and the form of the resolution. Oral announcement of the form of the resolution may be dispensed with by unanimous consent.\n>\n>(2) The time allotted for debate on a resolution offered from the floor as a question of the privileges of the House shall be equally divided between (A) the proponent of the resolution, and (B) the Majority Leader, the Minority Leader, or a designee, as determined by the Speaker.\n>\n>**(3) A resolution causing a vacancy in the Office of Speaker shall not be privileged except if offered by direction of a party caucus or conference.**\n>\n>(b) A question of personal privilege shall have precedence of all other questions except motions to adjourn."
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                "title": "Will an LLM pass an ARA evaluation before 2025?",
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            "id": 19104,
            "title": "Will Ukraine have de facto control of the Tokmak railway station on January 1, 2024?",
            "short_title": "Tokmak railway control on Jan 1, 2024",
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                "id": 19104,
                "title": "Will Ukraine have de facto control of the Tokmak railway station on January 1, 2024?",
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                "description": "Tokmak is a city in the Zaporizhzhia Oblast in Ukraine. It has a population of nearly 30,000. At the time of writing, it lies about 20km from the frontlines. The general purportedly leading Ukraine’s counteroffensive has said that liberating Tokmak is \"[the minimum goal](https://www.cnn.com/2023/09/23/europe/ukraine-biggest-counteroffensive-to-come-intl-hnk/index.html)” of the Ukrainian counteroffensive that started in June, 2023.",
                "resolution_criteria": "This question will resolve as Yes if, on January 1, 2024, the Institute for the Study of War's map shows the Velikiy Tokmak railway station in Tokmak ([47.234273433498416, 35.71907485774982](https://maps.app.goo.gl/hXQ4a9me5Pa8HwsF6)) as not under either \"assessed Russian advance\" or \"assessed Russian control\". Notably, the railway station is on the southern end of the town. \n\nIf the ISW ceases to publish this information or changes the naming conventions for the assessed territory, then Metaculus will decide according to information provided by ISW or other credible sources.\n\nIf, at the time of resolution, the Velikiy Tokmak railway station no longer stands at its current location or is fully destroyed, then this question will be resolved based on control of the area where the building was located on the 21st of February 2022, the [latest Google Earth image of the station available](https://earth.google.com/web/search/Velikij+Tokmak,+Zaporizhia+Oblast,+Ukraine/@47.23426725,35.71898701,75.01197177a,56.57951574d,35y,-0h,0t,0r/data=CigiJgokCbv42hx1n0dAESVTG6RZnEdAGR4NbapO30FAITn22SZL1kFAOgMKATA) at the time of writing.",
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                "title": "Before October 1, 2023, will US Senator Bob Menendez announce that he is resigning?",
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Massively parallelizing these assays will involve a highly systematic effort with a tightly coordinated and dedicated team, a substantial initial investment in gene-library synthesis and platform engineering, and long publishing timelines, which are qualities unsuitable for traditional grant funding. For these reasons, an FRO is the ideal (and probably the only viable) structure for this project.\n\n###How This Project Will Benefit Scientific Progress\nParadigm shifts in biology have often started with the humble bacteriophage. With 108-9 prospects across the oldest and most diverse host-pathogen interface in the biosphere, our FRO presents abundant opportunities for making impactful discoveries, and will pioneer a new field of functional metaviromics. 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This wealth of naturally engineered proteins holds the key to unlocking the full potential of the cell. Virus-derived genetic tools have driven most key advances in molecular biology, from recombinant DNA to CRISPR genetic engineering. Although most such transformative discoveries have resulted from the study of bacteriophages (viruses of bacteria), phage research has relied primarily on inferential work rather than systematic approaches to discern the functions of phage genes. With serendipity as the primary engine of discovery, experimental approaches have not kept pace with phage genome sequencing over the past decade. Consequently, the vast majority of phage genetic diversity is still entirely unexplored.\n\n###Project Concept\nWe have built a high throughput screening platform to characterize phage genes and completed a pilot of the entire pipeline, from gene selection through functional screening and mechanistic follow-up (manuscript in preparation and available upon request). 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FRO projects seek to produce transformative new tools, technologies, processes, or datasets that serve as public goods, creating new capabilities for the research community with the goal of accelerating scientific and technological progress more broadly. Crucially, FRO projects are those that often fall between the cracks left by existing research funding sources due to conflicting incentives, processes, mission, or culture. There are likely a large range of project concepts for which agencies could leverage FRO-style entities to achieve their mission and advance scientific progress.\n\nThis project is suited for a FRO-style approach because to achieve our scientific goals, we will need to scale our platform ~10,000-fold from 104-5 assays in the pilot to ~108-9 assays at the FRO. Massively parallelizing these assays will involve a highly systematic effort with a tightly coordinated and dedicated team, a substantial initial investment in gene-library synthesis and platform engineering, and long publishing timelines, which are qualities unsuitable for traditional grant funding. For these reasons, an FRO is the ideal (and probably the only viable) structure for this project.\n\n###How This Project Will Benefit Scientific Progress\nParadigm shifts in biology have often started with the humble bacteriophage. With 108-9 prospects across the oldest and most diverse host-pathogen interface in the biosphere, our FRO presents abundant opportunities for making impactful discoveries, and will pioneer a new field of functional metaviromics. 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                "resolution_criteria": "This question will resolve as **Yes** if, before January 1, 2050, credible sources report that the Russian Federation has placed an order for a US-made weapons system *and* that this order has been approved by the [US Department of State](https://www.state.gov/u-s-arms-sales-and-defense-trade/#:~:text=Sales%20are%20approved%20following%20U.S.,support%20being%20offered%20for%20delivery.), or through whatever other legal means necessary to approve American weapons sales to foreign nations present at that time. Only the order will need to placed to resolve this question as Yes; the weapons system need not actually be delivered to Russia. The weapons system must be purchased directly from the United States, not through a intermediary/third country. Credible sources reporting that the United States has approved providing weapons systems to Russia free of charge will also resolve this question as Yes. If this does not occur before the resolution date, the question resolves as **No**.\n\nFor the purpose of this question, the following are included in the definition of \"weapons system\":\n\n- Tanks\n- Armored fighting vehicles\n- Towed artillery\n- Self-propelled artillery\n- Rocket artillery\n- Surface-to-air missile systems\n- Military radars\n- Fighter and multi-role aircraft\n- Attack/bomber aircraft\n- Military helicopters\n- Combat drones/UCAVs\n- AWACS\n- Aerial refueling aircraft\n- Other aircraft intended solely for military use\n- Aircraft carriers\n- Naval destroyers\n- Cruisers\n- Frigates\n- Corvettes\n- Submarines\n- Guided missiles/launchers\n- Weapons of mass destruction\n- Any ammunition or components made to be used specifically by an American-produced version of the above\n\nMetaculus moderators may use their discretion to determine if a particular American export to Russia falls into the above categories or otherwise has no practical application outside a military setting, such that it must be considered a weapons system.",
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                "title": "Assuming the human molecular monitoring FRO is funded by 2025, will the milestone of developing a 100-analyte device for in situ monitoring be achieved before 2031?",
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                "description": "We recommend forecasters start with this document, [Forecasting Information for a “Focused Research Organization” to Develop a Modular and Scalable Platform for Human Molecular Monitoring](https://docs.google.com/document/d/1EJH6XDEOCbgQOTd8SaAHYglfq9h6GqNFlIlOroMaLWo/edit?usp=sharing).\n\n---\n\nFrom the [Federation of American Scientists](https://fas.org/publication/a-focused-research-organization-to-characterize-antibodies-through-open-science/):\n\nWearable health electronics are now ubiquitous, but continuous molecular monitoring is only widely available for glucose. Decades of research have expanded continuous monitoring to other molecules, but these techniques are restricted to research labs and remain disconnected from daily human use. We propose a platform to translate and distribute these emerging technologies, enabling the mapping of the time-varying human metabolome and the design of closed-loop devices for personalized health.\n\n###Problem Statement\nHumans are the best model organisms for humans, yet we have few tools to study human biochemistry in situ and in real time. The Human Metabolome Database lists ~20,000 detected compounds, of which only ~3,000 have been quantified. Even fewer of these biomolecules have been studied with time resolution in longitudinal human studies. \n\nCardiovascular, metabolic/endocrine and drug pharmacokinetic phenomena are driven by biomolecules varying on the time scale of seconds to minutes to hours, impacting behavior and well-being on similar time scales. Currently, the only way to measure these molecules is through laboratory testing, which is obtrusive to daily life. Moreover, laboratory testing cannot be conducted at the frequency necessary to capture all of these variations. \n\nIn contrast, wearable monitors are user-friendly and enable continuous measurements at the correct time scale. These monitors require specially engineered biosensors, since there are a limited number of naturally-occurring enzymes that generate continuous, time-varying electrical signals like those used by continuous glucose monitors, which are currently the only commercially available device of this kind. However, most labs that pioneer biosensing strategies do not develop human-compatible devices and vice versa, creating a chasm between these two areas of research and development.\n\n###Project Concept\nThis project aims to achieve minimally invasive continuous monitoring of 100+ analytes in the human body and deliver devices to researchers. This project will develop a medical device testbed that can use the myriad biosensing strategies pursued by academic labs to develop devices for human experiments. Our technical approach combines synthetic ion channels and conformational switches coupled with a CMOS array to assess many analytes in parallel. We already have access to customized fabrication techniques, and the cost and barriers in designing and manufacturing proteins and silicon sensors are trending downwards.\n\nThe project will progress through four interdependent stages:\n\nSurvey and prioritize metabolic, hormone, and immune targets that provide the greatest explanatory power for well-being. Select biosensor and transduction systems reported in the literature to interface with our platform.\nDevelop an integrated circuit functionalized with biosensors for parallel multi-analyte sensing packaged in a wearable form factor. Test devices in humans to validate against conventional blood sample analyses.\nSpecify and share validated devices in bulk to catalyze large-scale human field research.\nCurate a time-varying human metabolome.\n\n<a href=\"https://fas.org/wp-content/uploads/2023/08/Screen-Shot-2023-08-31-at-9.18.31-AM.png\">4 stages</a>\n\n###What Is A Focused Research Organization? \nFocused Research Organizations (FROs) are time-limited mission-focused research teams organized like a startup to tackle a specific mid-scale science or technology challenge. FRO projects seek to produce transformative new tools, technologies, processes, or datasets that serve as public goods, creating new capabilities for the research community with the goal of accelerating scientific and technological progress more broadly. Crucially, FRO projects are those that often fall between the cracks left by existing research funding sources due to conflicting incentives, processes, mission, or culture. There are likely a large range of project concepts for which agencies could leverage FRO-style entities to achieve their mission and advance scientific progress.\n\nThis project suits a FRO-style model because the four research stages require tight feedback loops and standardization and the medical device industry is not incentivized to pursue this kind of research. Private companies typically focus on a handful of molecules most relevant to diabetes care, taking advantage of proven biosensors and predictable insurance reimbursement. A stand-alone, non-profit institute is best suited to standardize and derisk experiments on molecular monitoring to catalyze the formation of a consortium of experimenters. Just as the nonprofit AddGene has standardized and democratized access to genetic material, we seek to develop the analog institution for medical devices.\n\n###How This Project Will Benefit Scientific Progress \nHuman physiology is currently a poorly explored, high-dimensional space, and scientific labs lack the tools to measure human biochemistry over time. The devices developed through this project will first help scientists study specific questions in domains such as disease etiology, human behavior, and drug discovery. Study validity will be enhanced by providing additional molecular time courses which will clarify the relationships between conditions, specific biomarkers, and interventions. Next, these studies will enable the development of a human molecular atlas, similar to the Human Metabolome Database but with time resolution. This database could act as a powerful tool for developing nuanced models of human physiology to uncover previously overlooked phenomena. Finally, similar devices will ultimately become accessible as consumer health products, enabling the next generation of personalized health.",
                "resolution_criteria": "This question resolves **Yes** if—before Jan 1, 2031—the following conditions are true:\n\n1. This FRO is funded at ≥$50M, according to reporting from the Federation of American Scientists\n\n2. The Federation of American Scientists says that the following milestone has been achieved:\n\n**Milestone 2: Develop a 100-analyte device for in situ monitoring**\n\nThe question can resolve **Yes** whether or not the milestone has been achieved by the proposed FRO to [develop a platform for human molecular monitoring](https://fas.org/publication/fro-scalable-molecular-monitoring/).",
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We propose a platform to translate and distribute these emerging technologies, enabling the mapping of the time-varying human metabolome and the design of closed-loop devices for personalized health.\n\n###Problem Statement\nHumans are the best model organisms for humans, yet we have few tools to study human biochemistry in situ and in real time. The Human Metabolome Database lists ~20,000 detected compounds, of which only ~3,000 have been quantified. Even fewer of these biomolecules have been studied with time resolution in longitudinal human studies. \n\nCardiovascular, metabolic/endocrine and drug pharmacokinetic phenomena are driven by biomolecules varying on the time scale of seconds to minutes to hours, impacting behavior and well-being on similar time scales. Currently, the only way to measure these molecules is through laboratory testing, which is obtrusive to daily life. Moreover, laboratory testing cannot be conducted at the frequency necessary to capture all of these variations. \n\nIn contrast, wearable monitors are user-friendly and enable continuous measurements at the correct time scale. These monitors require specially engineered biosensors, since there are a limited number of naturally-occurring enzymes that generate continuous, time-varying electrical signals like those used by continuous glucose monitors, which are currently the only commercially available device of this kind. However, most labs that pioneer biosensing strategies do not develop human-compatible devices and vice versa, creating a chasm between these two areas of research and development.\n\n###Project Concept\nThis project aims to achieve minimally invasive continuous monitoring of 100+ analytes in the human body and deliver devices to researchers. This project will develop a medical device testbed that can use the myriad biosensing strategies pursued by academic labs to develop devices for human experiments. Our technical approach combines synthetic ion channels and conformational switches coupled with a CMOS array to assess many analytes in parallel. We already have access to customized fabrication techniques, and the cost and barriers in designing and manufacturing proteins and silicon sensors are trending downwards.\n\nThe project will progress through four interdependent stages:\n\nSurvey and prioritize metabolic, hormone, and immune targets that provide the greatest explanatory power for well-being. Select biosensor and transduction systems reported in the literature to interface with our platform.\nDevelop an integrated circuit functionalized with biosensors for parallel multi-analyte sensing packaged in a wearable form factor. Test devices in humans to validate against conventional blood sample analyses.\nSpecify and share validated devices in bulk to catalyze large-scale human field research.\nCurate a time-varying human metabolome.\n\n<a href=\"https://fas.org/wp-content/uploads/2023/08/Screen-Shot-2023-08-31-at-9.18.31-AM.png\">4 stages</a>\n\n###What Is A Focused Research Organization? \nFocused Research Organizations (FROs) are time-limited mission-focused research teams organized like a startup to tackle a specific mid-scale science or technology challenge. FRO projects seek to produce transformative new tools, technologies, processes, or datasets that serve as public goods, creating new capabilities for the research community with the goal of accelerating scientific and technological progress more broadly. Crucially, FRO projects are those that often fall between the cracks left by existing research funding sources due to conflicting incentives, processes, mission, or culture. There are likely a large range of project concepts for which agencies could leverage FRO-style entities to achieve their mission and advance scientific progress.\n\nThis project suits a FRO-style model because the four research stages require tight feedback loops and standardization and the medical device industry is not incentivized to pursue this kind of research. Private companies typically focus on a handful of molecules most relevant to diabetes care, taking advantage of proven biosensors and predictable insurance reimbursement. A stand-alone, non-profit institute is best suited to standardize and derisk experiments on molecular monitoring to catalyze the formation of a consortium of experimenters. Just as the nonprofit AddGene has standardized and democratized access to genetic material, we seek to develop the analog institution for medical devices.\n\n###How This Project Will Benefit Scientific Progress \nHuman physiology is currently a poorly explored, high-dimensional space, and scientific labs lack the tools to measure human biochemistry over time. The devices developed through this project will first help scientists study specific questions in domains such as disease etiology, human behavior, and drug discovery. Study validity will be enhanced by providing additional molecular time courses which will clarify the relationships between conditions, specific biomarkers, and interventions. Next, these studies will enable the development of a human molecular atlas, similar to the Human Metabolome Database but with time resolution. This database could act as a powerful tool for developing nuanced models of human physiology to uncover previously overlooked phenomena. Finally, similar devices will ultimately become accessible as consumer health products, enabling the next generation of personalized health."
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We propose a platform to translate and distribute these emerging technologies, enabling the mapping of the time-varying human metabolome and the design of closed-loop devices for personalized health.\n\n###Problem Statement\nHumans are the best model organisms for humans, yet we have few tools to study human biochemistry in situ and in real time. The Human Metabolome Database lists ~20,000 detected compounds, of which only ~3,000 have been quantified. Even fewer of these biomolecules have been studied with time resolution in longitudinal human studies. \n\nCardiovascular, metabolic/endocrine and drug pharmacokinetic phenomena are driven by biomolecules varying on the time scale of seconds to minutes to hours, impacting behavior and well-being on similar time scales. Currently, the only way to measure these molecules is through laboratory testing, which is obtrusive to daily life. Moreover, laboratory testing cannot be conducted at the frequency necessary to capture all of these variations. \n\nIn contrast, wearable monitors are user-friendly and enable continuous measurements at the correct time scale. These monitors require specially engineered biosensors, since there are a limited number of naturally-occurring enzymes that generate continuous, time-varying electrical signals like those used by continuous glucose monitors, which are currently the only commercially available device of this kind. However, most labs that pioneer biosensing strategies do not develop human-compatible devices and vice versa, creating a chasm between these two areas of research and development.\n\n###Project Concept\nThis project aims to achieve minimally invasive continuous monitoring of 100+ analytes in the human body and deliver devices to researchers. This project will develop a medical device testbed that can use the myriad biosensing strategies pursued by academic labs to develop devices for human experiments. Our technical approach combines synthetic ion channels and conformational switches coupled with a CMOS array to assess many analytes in parallel. We already have access to customized fabrication techniques, and the cost and barriers in designing and manufacturing proteins and silicon sensors are trending downwards.\n\nThe project will progress through four interdependent stages:\n\nSurvey and prioritize metabolic, hormone, and immune targets that provide the greatest explanatory power for well-being. Select biosensor and transduction systems reported in the literature to interface with our platform.\nDevelop an integrated circuit functionalized with biosensors for parallel multi-analyte sensing packaged in a wearable form factor. Test devices in humans to validate against conventional blood sample analyses.\nSpecify and share validated devices in bulk to catalyze large-scale human field research.\nCurate a time-varying human metabolome.\n\n<a href=\"https://fas.org/wp-content/uploads/2023/08/Screen-Shot-2023-08-31-at-9.18.31-AM.png\">4 stages</a>\n\n###What Is A Focused Research Organization? \nFocused Research Organizations (FROs) are time-limited mission-focused research teams organized like a startup to tackle a specific mid-scale science or technology challenge. FRO projects seek to produce transformative new tools, technologies, processes, or datasets that serve as public goods, creating new capabilities for the research community with the goal of accelerating scientific and technological progress more broadly. Crucially, FRO projects are those that often fall between the cracks left by existing research funding sources due to conflicting incentives, processes, mission, or culture. There are likely a large range of project concepts for which agencies could leverage FRO-style entities to achieve their mission and advance scientific progress.\n\nThis project suits a FRO-style model because the four research stages require tight feedback loops and standardization and the medical device industry is not incentivized to pursue this kind of research. Private companies typically focus on a handful of molecules most relevant to diabetes care, taking advantage of proven biosensors and predictable insurance reimbursement. A stand-alone, non-profit institute is best suited to standardize and derisk experiments on molecular monitoring to catalyze the formation of a consortium of experimenters. Just as the nonprofit AddGene has standardized and democratized access to genetic material, we seek to develop the analog institution for medical devices.\n\n###How This Project Will Benefit Scientific Progress \nHuman physiology is currently a poorly explored, high-dimensional space, and scientific labs lack the tools to measure human biochemistry over time. The devices developed through this project will first help scientists study specific questions in domains such as disease etiology, human behavior, and drug discovery. Study validity will be enhanced by providing additional molecular time courses which will clarify the relationships between conditions, specific biomarkers, and interventions. Next, these studies will enable the development of a human molecular atlas, similar to the Human Metabolome Database but with time resolution. This database could act as a powerful tool for developing nuanced models of human physiology to uncover previously overlooked phenomena. Finally, similar devices will ultimately become accessible as consumer health products, enabling the next generation of personalized health.",
                "resolution_criteria": "This question resolves **Yes** if—before Jan 1, 2031—the following conditions are true:\n\n1. This FRO is funded at ≥$50M, according to reporting from the Federation of American Scientists\n\n2. The Federation of American Scientists says that the following milestone has been achieved:\n\n**Milestone 1: Develop a 10-analyte device for in situ monitoring **\n\nThe question can resolve **Yes** whether or not the milestone has been achieved by the proposed FRO to [develop a platform for human molecular monitoring](https://fas.org/publication/fro-scalable-molecular-monitoring/).",
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We propose a platform to translate and distribute these emerging technologies, enabling the mapping of the time-varying human metabolome and the design of closed-loop devices for personalized health.\n\n###Problem Statement\nHumans are the best model organisms for humans, yet we have few tools to study human biochemistry in situ and in real time. The Human Metabolome Database lists ~20,000 detected compounds, of which only ~3,000 have been quantified. Even fewer of these biomolecules have been studied with time resolution in longitudinal human studies. \n\nCardiovascular, metabolic/endocrine and drug pharmacokinetic phenomena are driven by biomolecules varying on the time scale of seconds to minutes to hours, impacting behavior and well-being on similar time scales. Currently, the only way to measure these molecules is through laboratory testing, which is obtrusive to daily life. Moreover, laboratory testing cannot be conducted at the frequency necessary to capture all of these variations. \n\nIn contrast, wearable monitors are user-friendly and enable continuous measurements at the correct time scale. These monitors require specially engineered biosensors, since there are a limited number of naturally-occurring enzymes that generate continuous, time-varying electrical signals like those used by continuous glucose monitors, which are currently the only commercially available device of this kind. However, most labs that pioneer biosensing strategies do not develop human-compatible devices and vice versa, creating a chasm between these two areas of research and development.\n\n###Project Concept\nThis project aims to achieve minimally invasive continuous monitoring of 100+ analytes in the human body and deliver devices to researchers. This project will develop a medical device testbed that can use the myriad biosensing strategies pursued by academic labs to develop devices for human experiments. Our technical approach combines synthetic ion channels and conformational switches coupled with a CMOS array to assess many analytes in parallel. We already have access to customized fabrication techniques, and the cost and barriers in designing and manufacturing proteins and silicon sensors are trending downwards.\n\nThe project will progress through four interdependent stages:\n\nSurvey and prioritize metabolic, hormone, and immune targets that provide the greatest explanatory power for well-being. Select biosensor and transduction systems reported in the literature to interface with our platform.\nDevelop an integrated circuit functionalized with biosensors for parallel multi-analyte sensing packaged in a wearable form factor. Test devices in humans to validate against conventional blood sample analyses.\nSpecify and share validated devices in bulk to catalyze large-scale human field research.\nCurate a time-varying human metabolome.\n\n<a href=\"https://fas.org/wp-content/uploads/2023/08/Screen-Shot-2023-08-31-at-9.18.31-AM.png\">4 stages</a>\n\n###What Is A Focused Research Organization? \nFocused Research Organizations (FROs) are time-limited mission-focused research teams organized like a startup to tackle a specific mid-scale science or technology challenge. FRO projects seek to produce transformative new tools, technologies, processes, or datasets that serve as public goods, creating new capabilities for the research community with the goal of accelerating scientific and technological progress more broadly. Crucially, FRO projects are those that often fall between the cracks left by existing research funding sources due to conflicting incentives, processes, mission, or culture. There are likely a large range of project concepts for which agencies could leverage FRO-style entities to achieve their mission and advance scientific progress.\n\nThis project suits a FRO-style model because the four research stages require tight feedback loops and standardization and the medical device industry is not incentivized to pursue this kind of research. Private companies typically focus on a handful of molecules most relevant to diabetes care, taking advantage of proven biosensors and predictable insurance reimbursement. A stand-alone, non-profit institute is best suited to standardize and derisk experiments on molecular monitoring to catalyze the formation of a consortium of experimenters. Just as the nonprofit AddGene has standardized and democratized access to genetic material, we seek to develop the analog institution for medical devices.\n\n###How This Project Will Benefit Scientific Progress \nHuman physiology is currently a poorly explored, high-dimensional space, and scientific labs lack the tools to measure human biochemistry over time. The devices developed through this project will first help scientists study specific questions in domains such as disease etiology, human behavior, and drug discovery. Study validity will be enhanced by providing additional molecular time courses which will clarify the relationships between conditions, specific biomarkers, and interventions. Next, these studies will enable the development of a human molecular atlas, similar to the Human Metabolome Database but with time resolution. This database could act as a powerful tool for developing nuanced models of human physiology to uncover previously overlooked phenomena. Finally, similar devices will ultimately become accessible as consumer health products, enabling the next generation of personalized health."
        }
    ]
}