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=3420
HTTP 200 OK
Allow: GET, OPTIONS
Content-Type: application/json
Vary: Accept

{
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    "next": "http://www.metaculus.com/api2/questions/?format=api&limit=20&offset=3440",
    "previous": "http://www.metaculus.com/api2/questions/?format=api&limit=20&offset=3400",
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                "id": 19192,
                "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.",
                "resolution_criteria": "This question will resolve as **Yes** if, after November 15, 2023, and before January 1, 2024, MONUSCO's mission has been renewed or extended with a troop ceiling of 11,000 \"military personnel\" or more.",
                "fine_print": "* Only the troop ceiling for \"military personnel\" will be counted for this question, other personnel such as military observers and staff officers, police personnel, or personnel of formed police units will be immaterial.\n* Actual deployed strength is immaterial to the question, this question only refers to the the authorized troop ceiling on \"military personnel\".\n* If the mandate is not renewed or otherwise extended this question will resolve as **No**.\n* The question will still resolve as **Yes** if the renewal or extension is referred to as something other than a mandate, so long as MONUSCO's mission in the DRC is extended for any period of time with a qualifying troop ceiling.",
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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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                "description": "The [Alignment Research Center](https://www.alignment.org) (ARC) runs a project called [ARC Evals](https://evals.alignment.org) that evaluates AI systems to see if they pose a catastrophic risk to the human species. [Update: [ARC Evals has spun out from ARC](https://metr.org/blog/2023-12-04-metr-announcement/), and has renamed to METR.] As can be seen from [this report](https://evals.alignment.org/blog/2023-08-01-new-report/), ARC has introduced \"methodology for assessing the capacity of LLM agents to acquire resources, create copies of themselves, and adapt to novel challenges they encounter in the wild.\" Also, as noted in the report, OpenAI's GPT-4 and Anthropic's Claude are not currently capable of passing the ARA evaluation.\n\nThis questions aims to determine the likelihood of an AI model passing the autonomous replication and adaptation—ARA—evaluation before 2025, because this would present a worrying development for the capability of an AI model to inflict major harm on human civilization.",
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                "resolution_criteria": "This question will resolve as Yes, if before the first vote cast for the next Indian general election, at least 75% of contesting [Lok Sabha](https://en.wikipedia.org/wiki/Lok_Sabha) candidates from any one of the [Indian National Congress](https://en.wikipedia.org/wiki/Indian_National_Congress), the [Aam Aadmi Party](https://en.wikipedia.org/wiki/Aam_Aadmi_Party), the [Communist Party of India (Marxist)](https://en.wikipedia.org/wiki/Communist_Party_of_India_(Marxist)) the [All India Trinamool Congress](https://en.wikipedia.org/wiki/Trinamool_Congress), the [Janata Dal (United)](https://en.wikipedia.org/wiki/Janata_Dal_(United)) the [Samajwadi Party](https://en.wikipedia.org/wiki/Samajwadi_Party) or the [Dravida Munnetra Kazhagam](https://en.wikipedia.org/wiki/Dravida_Munnetra_Kazhagam) (who are members of these parties as of 01/10/2023), do not contest under the I.N.D.I.A. alliance. If the I.N.D.I.A. factionalizes into 2 or more constituents, with the largest constituent not having at least 25% of contesting Lok Sabha candidates from each of the above parties, this question will also resolve as Yes.",
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                "title": "Before October 1, 2023, will US Senator Bob Menendez announce that he is resigning?",
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                "description": "We recommend forecasters start with this document, [Forecasting Information for a “Focused Research Organization” to Systematically Study Bacteriophage Genes and Their Functions](https://docs.google.com/document/d/18gATtTOlUspz_na5AfNLwZDy2NXdkyvob5PNsqHidXs/edit#heading=h.za66qtpqyic8).\n\n---\n\nFrom the [Federation of American Scientists](https://fas.org/publication/a-focused-research-organization-to-systematically-study-bacteriophage-genes-and-their-functions/):\n\nSystematically sequencing the genome and studying the function of genes from all viruses that infect a set of model bacteria with significant scientific, biotechnological, and human health relevance will enable the development of phage-gene libraries that can in turn enable the faster development of genetic tools for advancing molecular biology.\n\n###Problem Statement\nViruses have been evolving host-modifying factors for billions of years. 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). Our FRO will scale this platform and use it to chemically synthesize and test all non-redundant phage genes from two clinically relevant families of bacteria (Enterobacteria and Mycobacteria) which collectively host ~40% of all isolated phages, allowing us to test a large swathe of phage genetic diversity in a set of model species. The phage-gene library generated from this process will enable us to pursue the following objectives: 1) discover new molecular tools with revolutionary potential (eg. broadly understanding the principles of protein detection in antiviral immunity could yield a generalizable protein-targeting framework without some of the pitfalls of antibodies), 2) develop therapeutic avenues for antimicrobial resistant infections inspired by natural antiviral defense and counter-defense strategies, 3) build an inventory of phage design principles and engineering methods for therapeutic, industrial, and microbiome-directed applications, and 4) gain a complete understanding of interactions between phage and their hosts.\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 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. Moreover, the phage-gene libraries we will create are analogous to small-molecule screening libraries, consisting of 104-105 phage-derived natural products that can be used to find potentiators or suppressors of any cellular stressor of interest. We expect these resources to enable discovery far beyond the scope and timeline of our FRO.",
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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). Our FRO will scale this platform and use it to chemically synthesize and test all non-redundant phage genes from two clinically relevant families of bacteria (Enterobacteria and Mycobacteria) which collectively host ~40% of all isolated phages, allowing us to test a large swathe of phage genetic diversity in a set of model species. The phage-gene library generated from this process will enable us to pursue the following objectives: 1) discover new molecular tools with revolutionary potential (eg. broadly understanding the principles of protein detection in antiviral immunity could yield a generalizable protein-targeting framework without some of the pitfalls of antibodies), 2) develop therapeutic avenues for antimicrobial resistant infections inspired by natural antiviral defense and counter-defense strategies, 3) build an inventory of phage design principles and engineering methods for therapeutic, industrial, and microbiome-directed applications, and 4) gain a complete understanding of interactions between phage and their hosts.\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 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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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). Our FRO will scale this platform and use it to chemically synthesize and test all non-redundant phage genes from two clinically relevant families of bacteria (Enterobacteria and Mycobacteria) which collectively host ~40% of all isolated phages, allowing us to test a large swathe of phage genetic diversity in a set of model species. The phage-gene library generated from this process will enable us to pursue the following objectives: 1) discover new molecular tools with revolutionary potential (eg. broadly understanding the principles of protein detection in antiviral immunity could yield a generalizable protein-targeting framework without some of the pitfalls of antibodies), 2) develop therapeutic avenues for antimicrobial resistant infections inspired by natural antiviral defense and counter-defense strategies, 3) build an inventory of phage design principles and engineering methods for therapeutic, industrial, and microbiome-directed applications, and 4) gain a complete understanding of interactions between phage and their hosts.\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 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. Moreover, the phage-gene libraries we will create are analogous to small-molecule screening libraries, consisting of 104-105 phage-derived natural products that can be used to find potentiators or suppressors of any cellular stressor of interest. We expect these resources to enable discovery far beyond the scope and timeline of our FRO."
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            "id": 19055,
            "title": "Will Russia purchase an American weapons system before 2050?",
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                "title": "Will Russia purchase an American weapons system before 2050?",
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                "description": "Weapons sales from one country to another are often a useful indicator of positive geopolitical ties between those two nations. The logic behind this is that nations won't export weapons to other countries which visibly seek to compete with them militarily. For example, European NATO states make [extensive purchases](https://www.statista.com/statistics/248552/us-arms-exports-by-country/) of American weapons due to the United States's dominant position in the alliance. Likewise, Russian-allied countries such as Belarus and Kazakhstan [rely heavily](https://www.statista.com/statistics/1102702/countries-where-russia-is-a-major-arms-supplier/) on weapons imports from Russia to maintain their armed forces. \n\nIn the context of Russian-American relations, Russia purchasing American weapons systems would indicate the United States' strategic interests aligning more with those of Russia than they currently do, and vice versa. Moreover, it would indicate improvements in geopolitical ties between these two countries. This could occur as a result of changes in the political landscape of either country, external threats posed to both nations, or a number of other things.",
                "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.",
                "fine_print": "If the United States or Russian Federation cease to exist in their current form prior to the resolution date (as determined by Metaculus moderators), this question will resolve as **Ambiguous**.",
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            "description": "Weapons sales from one country to another are often a useful indicator of positive geopolitical ties between those two nations. The logic behind this is that nations won't export weapons to other countries which visibly seek to compete with them militarily. For example, European NATO states make [extensive purchases](https://www.statista.com/statistics/248552/us-arms-exports-by-country/) of American weapons due to the United States's dominant position in the alliance. Likewise, Russian-allied countries such as Belarus and Kazakhstan [rely heavily](https://www.statista.com/statistics/1102702/countries-where-russia-is-a-major-arms-supplier/) on weapons imports from Russia to maintain their armed forces. \n\nIn the context of Russian-American relations, Russia purchasing American weapons systems would indicate the United States' strategic interests aligning more with those of Russia than they currently do, and vice versa. Moreover, it would indicate improvements in geopolitical ties between these two countries. This could occur as a result of changes in the political landscape of either country, external threats posed to both nations, or a number of other things."
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            "id": 19038,
            "title": "By December 31st, 2028, will it be considered best practice in clinical psychology to incorporate AI tools in the diagnostic process?",
            "short_title": "AI: Best Practice in Psychology by 2028",
            "url_title": "AI: Best Practice in Psychology by 2028",
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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 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. 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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. 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                "title": "Assuming the human molecular monitoring FRO is funded by 2025, will the milestone of developing a 10-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 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. 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Finally, similar devices will ultimately become accessible as consumer health products, enabling the next generation of personalized health."
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