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=5000
HTTP 200 OK
Allow: GET, OPTIONS
Content-Type: application/json
Vary: Accept

{
    "count": 6400,
    "next": "http://www.metaculus.com/api2/questions/?format=api&limit=20&offset=5020",
    "previous": "http://www.metaculus.com/api2/questions/?format=api&limit=20&offset=4980",
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                "id": 6558,
                "title": "Will a functional Alcubierre drive-like FTL device be demonstrated before 2100?",
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                "resolution_criteria": "[The Alcubierre drive](https://en.wikipedia.org/wiki/Alcubierre_drive) is a speculative warp drive idea based on a solution of Einstein's field equations in general relativity as proposed by Mexican theoretical physicist Miguel Alcubierre, by which a spacecraft could achieve apparent faster-than-light travel if a configurable energy-density field lower than that of vacuum (that is, negative mass) could be created.\n\nRather than exceeding the speed of light within a local reference frame, a spacecraft would traverse distances by contracting space in front of it and expanding space behind it, resulting in effective faster-than-light travel. Objects cannot accelerate to the speed of light within normal spacetime; instead, the Alcubierre drive shifts space around an object so that the object would arrive at its destination more quickly than light would in normal space without breaking any physical laws.\n\nHowever, there are [a number of technical challenges](https://en.wikipedia.org/wiki/Alcubierre_drive#Difficulties) that may mean that it is either extremely difficult or impossible to create a device that functions as Alcubierre described.\n\nAlcubierre's original paper can be read here: [The warp drive: hyper-fast travel within general relativity](https://arxiv.org/abs/gr-qc/0009013)\n\n***Will a functional Alcubierre drive device be demonstrated before 2100?***\n\nThis question will resolve as **Yes** if before January 1, 2100, a credible paper is published in a peer-reviewed journal that details a successful demonstration of a functioning device that works broadly in the manner that Alcubierre described, and that enables a physical object to traverse distances at faster-than-light speeds.\n\nThis demonstration must take place in 'base reality' (i.e. the universe in which the concept was originally proposed, and in which Metaculus users in January 2021 lived) rather than in any kind of simulated reality or alternative physical universe that is created or discovered after February 12, 2021.",
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                "description": "From the Impossible Foods [FAQ](https://faq.impossiblefoods.com/hc/en-us/articles/360019100553-What-is-soy-leghemoglobin-or-heme-),\n\n> Although heme has been consumed every day for hundreds of thousands of years, Impossible Foods discovered that it’s what makes meat taste so meaty.\n\n\nFrom [Food Safety News](https://www.foodsafetynews.com/2021/02/lawsuit-challenges-fda-approval-of-additive-that-makes-impossible-burger-bleed/),\n\n> The Center for Food Safety is challenging the FDA’s approval of a color additive used to make Impossible Foods’ plant-based burger appear to “bleed” like real meat. The advocacy group claims that the FDA’s decision was not based on “convincing evidence” as required by regulation.\n\n> In a brief filed Jan. 28 in the Ninth Circuit U.S. Court of Appeals, the center is specifically challenging the Food and Drug Administration’s 2019 approval of soy leghemoglobin.\n\n> “This includes studies for cancer, reproductive impairment and other adverse effects called for by FDA’s Redbook, the Bible of food and color additive testing. We find this to be all the more troubling because a number of potential adverse effects were detected in a short-term rat trial: disruption of reproductive cycles and reduced uterine weights in females and biomarkers of anemia, reduced clotting ability and kidney problems.”\n\n> The novel “heme” colorant is produced in genetically engineered (GE) yeast and is modeled on a protein found in the roots of soybeans. The ingredient is also referred to as genetically engineered “heme,” soy leghemoglobin. It is the color additive Impossible Foods uses to make its plant-based burger appear to “bleed” as if it were beef. \n\nFrom Wikipedia, the Center for Food Safety [is](https://en.wikipedia.org/wiki/Center_for_Food_Safety),\n\n> a 501c3, U.S. non-profit advocacy organization, based in Washington, D.C. It maintains an office in San Francisco, California. The executive director is Andrew Kimbrell, an attorney. Its stated mission is to protect human health and the environment, focusing on food production technologies such as genetically modified plants and organisms (GMOs). It was founded in 1997.\n\nYou can read the brief filed with the Ninth Circuit U.S. Court of Appeals [here](https://www.centerforfoodsafety.org/files/2021-01-28--ecf-45-cfs-combined-reply-brief_82674.pdf).",
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            "description": "The University of Pennsylvania decided to allow undergraduate students to come onto campus. They [announced](https://coronavirus.upenn.edu/announcement/planning-penn%E2%80%99s-spring-2021-semester) this policy in October. Further details on their campus policies for the semester can be found [here](https://coronavirus.upenn.edu/announcement/message-penn-community-0). However, the university has recently reported a [surge](https://coronavirus.upenn.edu/content/dashboard) in cases among the undergraduate. This has led some to reflect on the possibility that the university might close the campus (see [this editorial](https://www.thedp.com/article/2021/02/upenn-compact-violations-covid-philadelphia-partying-ivy-league) from the school's newspaper). Thus, my question is whether the university will declare an Alert Level 4 (sending students home) before May 11 (the final day of the spring semester)."
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                "title": "[Short Fuse] Will SpaceX's SN10 Starship prototype vehicle land successfully?",
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                "resolution_criteria": "SpaceX is currently developing [Starship](https://en.wikipedia.org/wiki/SpaceX_Starship) - a two-stage, reusable launch system intended to one day bring humans to Mars.\n\nOn December 8th 2020, Starship SN8 was the first SpaceX Starship prototype to fly to a height of at least 1 km.\n\nOn Feburary 2nd 2021, Starship SN9 was the second prototype to do so.\n\nBoth SN8 and SN9 failed to land successfully, exploding on impact. \n\nThe cause of SN8's failure is thought to be [fuel tank underpressure](https://twitter.com/elonmusk/status/1336809767574982658), causing oxygen-rich combustion to overheat and destroy one engine.\n\nThe cause of SN9's failure was that one of the two Raptor engines used for the attempted landing failed to re-light for the landing burn.\n\nWhen asked why SN9 did not re-light all three engines, and subsequently shut-off one of them if all three re-lit successfully, Elon Musk responded that [It was foolish of us not to start 3 engines & immediately shut down 1, as 2 are needed to land](https://twitter.com/elonmusk/status/1357422126161145856).\n\nThe Starship SN10 prototype is currently on the launch pad being fitted with Raptor engines, and [is expected to fly soon](https://www.metaculus.com/questions/6340/when-will-the-third-starship-flight-be/).\n\n***Will SpaceX's SN10 Starship prototype vehicle land successfully?***\n\nThis question will resolve positively if the Starship SN10 prototype flies to an altitude of at least 1km and successfully lands.\n\nIf Starship SN10 has not flown yet by the resolution date, this question resolves ambiguous.\n\nIf Starship SN10 is destroyed without flying to an altitude of at least 1km, or if SpaceX announces that it does not intend to fly SN10 after all, then this question resolves negative.\n\nThe landing will be considered successful or unsuccessful if it is described as such by SpaceX or Elon Musk (they do not need to use those exact words), if neither comments on the success of the landing, then by two reliable media sources.",
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                "title": "Will the single-dose Johnson & Johnson SARS-CoV-2 vaccine be issued an emergency use authorization by the US FDA within a week after the 26 February VRBPAC meeting?",
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                "description": "The single-dose adenovirus-vectored vaccine Ad26.COV2.S, which encodes the spike protein of SARS-CoV-2, is currently undergoing [Phase III testing](https://clinicaltrials.gov/ct2/show/NCT04505722) with the support of Johnson & Johnson. This randomized double-blind Phase III trial, known as ENSEMBLE, has enrolled [45,000 adult participants](https://www.jnj.com/innovation/questions-about-johnson-johnson-investigational-covid-19-vaccine) in [multiple countries](https://www.jnj.com/johnson-johnson-initiates-pivotal-global-phase-3-clinical-trial-of-janssens-covid-19-vaccine-candidate). \n\nOn 29 January, Johnson & Johnson [reported interim results](https://www.jnj.com/johnson-johnson-announces-single-shot-janssen-covid-19-vaccine-candidate-met-primary-endpoints-in-interim-analysis-of-its-phase-3-ensemble-trial) from the ENSEMBLE trial, which includes 72% efficacy in the US and 66% overall efficacy against moderate to severe COVID-19.\n\nOn 4 February, Johnson & Johnson [announced](https://www.janssen.com/johnson-johnson-announces-submission-application-us-fda-emergency-use-authorization-its) that it had submitted an application to the U.S. Food and Drug Administration (FDA) requesting [Emergency Use Authorization (EUA)](https://www.fda.gov/vaccines-blood-biologics/vaccines/emergency-use-authorization-vaccines-explained) Later on 4 February, the FDA [scheduled a meeting](https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-announces-advisory-committee-meeting-discuss-janssen-biotech-incs?utm_medium=email&utm_source=govdelivery) of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) for 26 February 2021. The purpose of the VRBPAC meeting is to have a [\"public discussion ... about the data submitted in support of safety and effectiveness of Janssen Biotech Inc.’s COVID-19 vaccine ... help ensure that the public has a clear understanding of the scientific data and information that FDA will evaluate in order to make a decision about whether to authorize this vaccine.\"](https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-announces-advisory-committee-meeting-discuss-janssen-biotech-incs?utm_medium=email&utm_source=govdelivery)\n\nFor the two SARS-CoV-2 vaccines for which the FDA has already issued EUAs, the EUA was issued the day after the VRBPAC meeting. The VRBPAC meeting on the Pfizer-BioNTech vaccine occurred on [10 December 2020](https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-december-10-2020-meeting-announcement) and the FDA issued an EUA for it on [11 December](https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine). The VRBPAC meeting on the Moderna vaccine occurred on [17 December 2020](https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-december-17-2020-meeting-announcement) and the FDA issued an EUA for it on [18 December](https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/moderna-covid-19-vaccine).",
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            "description": "The single-dose adenovirus-vectored vaccine Ad26.COV2.S, which encodes the spike protein of SARS-CoV-2, is currently undergoing [Phase III testing](https://clinicaltrials.gov/ct2/show/NCT04505722) with the support of Johnson & Johnson. This randomized double-blind Phase III trial, known as ENSEMBLE, has enrolled [45,000 adult participants](https://www.jnj.com/innovation/questions-about-johnson-johnson-investigational-covid-19-vaccine) in [multiple countries](https://www.jnj.com/johnson-johnson-initiates-pivotal-global-phase-3-clinical-trial-of-janssens-covid-19-vaccine-candidate). \n\nOn 29 January, Johnson & Johnson [reported interim results](https://www.jnj.com/johnson-johnson-announces-single-shot-janssen-covid-19-vaccine-candidate-met-primary-endpoints-in-interim-analysis-of-its-phase-3-ensemble-trial) from the ENSEMBLE trial, which includes 72% efficacy in the US and 66% overall efficacy against moderate to severe COVID-19.\n\nOn 4 February, Johnson & Johnson [announced](https://www.janssen.com/johnson-johnson-announces-submission-application-us-fda-emergency-use-authorization-its) that it had submitted an application to the U.S. Food and Drug Administration (FDA) requesting [Emergency Use Authorization (EUA)](https://www.fda.gov/vaccines-blood-biologics/vaccines/emergency-use-authorization-vaccines-explained) Later on 4 February, the FDA [scheduled a meeting](https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-announces-advisory-committee-meeting-discuss-janssen-biotech-incs?utm_medium=email&utm_source=govdelivery) of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) for 26 February 2021. The purpose of the VRBPAC meeting is to have a [\"public discussion ... about the data submitted in support of safety and effectiveness of Janssen Biotech Inc.’s COVID-19 vaccine ... help ensure that the public has a clear understanding of the scientific data and information that FDA will evaluate in order to make a decision about whether to authorize this vaccine.\"](https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-announces-advisory-committee-meeting-discuss-janssen-biotech-incs?utm_medium=email&utm_source=govdelivery)\n\nFor the two SARS-CoV-2 vaccines for which the FDA has already issued EUAs, the EUA was issued the day after the VRBPAC meeting. The VRBPAC meeting on the Pfizer-BioNTech vaccine occurred on [10 December 2020](https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-december-10-2020-meeting-announcement) and the FDA issued an EUA for it on [11 December](https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/pfizer-biontech-covid-19-vaccine). The VRBPAC meeting on the Moderna vaccine occurred on [17 December 2020](https://www.fda.gov/advisory-committees/advisory-committee-calendar/vaccines-and-related-biological-products-advisory-committee-december-17-2020-meeting-announcement) and the FDA issued an EUA for it on [18 December](https://www.fda.gov/emergency-preparedness-and-response/coronavirus-disease-2019-covid-19/moderna-covid-19-vaccine)."
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                "title": "Will there be adversarial use of consumer genomic data before 2030?",
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                "description": "Genetic sequencing has gotten cheaper by [several orders of magnitude](https://www.genome.gov/about-genomics/fact-sheets/Sequencing-Human-Genome-cost) in the past several decades. [Over 1 million Americans](https://phys.org/news/2018-10-people-dna-sequenced-theyve-privacy.html) have already had their DNA sequenced through direct-to-consumer products like those offered by 23AndMe, Ancestry, etc.\n\n[Many concerns](https://www.washingtonpost.com/health/dna-tests-privacy-risks/2020/09/11/6a783a34-d73b-11ea-9c3b-dfc394c03988_story.html) have been raised about possible harms. While it is illegal in the United States to use genomics data to set health insurance rates or discriminate for employment, there are related other uses not covered (other types of insurance or discrimination) as well as more speculative ideas. For example, if an adversary had access to your genetic data, they might be able to forge evidence tying you to a particular crime, or might be able to fool a biometric identification system.\n\nNote: I am using \"DNA data\", \"genomics data\", \"genetic data\" interchangeably here, but I am not an expert. Please help clarify if this is incorrect.",
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                "description": "*What would a Trump administration look like? A Harris administration? What would be dramatically different, and what would be the same? Learn more in the [2024 Electoral Consequences series](https://www.metaculus.com/project/us-conditionals/).*\n\nEvery 4 years, the United States elects a president with its unique system of [the Electoral College](https://en.wikipedia.org/wiki/United_States_Electoral_College).  A candidate must secure 270 or more electoral college votes out of 538, or be [selected by Congress](https://www.youtube.com/watch?v=sHEDXzOfENI) if no candidate receives more than 269 votes.\n\nThe [2020 election](https://en.wikipedia.org/wiki/2020_United_States_presidential_election) ended with President Donald Trump losing his run for a second term.  He immediately and repeatedly made claims the election was rigged and fraudulent, which led to the [January 6 storming of the Capitol](https://en.wikipedia.org/wiki/2021_storming_of_the_United_States_Capitol).  Ultimately, the votes were confirmed by Congress and Joe Biden was inaugurated on January 20, 2021.\n\nBiden faces several challenges entering his presidency, including the [COVID-19 pandemic](https://ourworldindata.org/coronavirus) and [an unemployment rate](https://www.bls.gov/charts/employment-situation/civilian-unemployment-rate.htm) of 6.7%, with a [narrow majority](https://en.wikipedia.org/wiki/117th_United_States_Congress) in Congress to pass legislation.  Biden began his presidency with a [historically high disapproval rating](https://projects.fivethirtyeight.com/biden-approval-rating/) of 35%, indicating that we are in a period of high partisanship and [highly competitive elections](https://fivethirtyeight.com/features/why-a-biden-blowout-didnt-happen-and-why-a-2024-blowout-is-unlikely-too/).  On the other hand, politicians generally have an incumbency advantage, which could mean a likely victory for Biden.",
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