{
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   "id": 14,
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   "question": "\"What percentage of glioblastoma patients have alterations in RB pathway genes (CDKN2A, CDK4, RB1)?\"",
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   "id": 64,
   "question": "In TCGA PanCancer Atlas, which recurrent hotspot mutations occur almost exclusively in one cancer type?",
   "category": "Variants & hotspots",
   "track": "analysis",
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   "id": 66,
   "question": "In colorectal cancer do patients with microsatellite instability in the TCGA dataset have a similar prognosis as those in the MSK Gastroenterology 2020 study?",
   "category": "Survival & outcomes",
   "track": "analysis",
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  {
   "id": 76,
   "question": "Are TP53 mutations clinically actionable?",
   "category": "Out of scope",
   "track": "out_of_scope",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
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  {
   "id": 78,
   "question": "what's the best way to put clinical data into cbioportal?",
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   "mismatch": [],
   "a": {
    "expected": 1,
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  {
   "id": 79,
   "question": "Can you please generate a survival curve for colorectal cancer patients based on the expression levels of IMPDH2?",
   "category": "Survival & outcomes",
   "track": "navigation",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
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  {
   "id": 81,
   "question": "tell me about IDH1 mutations in glioma",
   "category": "Alteration frequency",
   "track": "data",
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   "id": 83,
   "question": "Help me rank TCGA cancer studies based on median CD3 expression",
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  {
   "id": 84,
   "question": "Can you analyze thyroid hormone gene expression by diagnosis in the Pediatric Brain Tumor Atlas (PBTA, Provisional) cohort?",
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   "track": "out_of_scope",
   "gradeable": true,
   "mismatch": [],
   "a": {
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  {
   "id": 91,
   "question": "show me a histogram of C228T mutations in the tert promoter across cancer types",
   "category": "Variants & hotspots",
   "track": "navigation",
   "gradeable": true,
   "mismatch": [],
   "a": {
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   "delta": -100.0,
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  {
   "id": 92,
   "question": "what is the most prevalent TP53 mutation in uterine cancer that is not a point mutation",
   "category": "Variants & hotspots",
   "track": "data",
   "gradeable": true,
   "mismatch": [],
   "a": {
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   "b": {
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   "id": 94,
   "question": "There is a heavily discussed driver alteration in MAP2K1 at codon 105 that significantly alters mRNA stability. Please list the expression values for the tumors that have a nucleotide change at this position",
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   "track": "data",
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    "fast_share_all": 100.0,
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    "fast_share_all": 100.0,
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  {
   "id": 96,
   "question": "Is KRAS G12C more aggressive than G12D?",
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   "track": "analysis",
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   "mismatch": [],
   "a": {
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  {
   "id": 108,
   "question": "Can you find a study that I may emulate that has a data_clinical_outcomes.txt file and associated meta file to interogate",
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  {
   "id": 113,
   "question": "In lower grade glioma, are there genes which are overexpressed in any of the molecular subtypes?",
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  {
   "id": 118,
   "question": "In TCGA lower grade glioma, show me IDH1 mRNA expression by IDH1 mutation status.",
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  {
   "id": 134,
   "question": "compare egfr mutations between lung and brain cancer",
   "category": "Alteration frequency",
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   "a": {
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   "b": {
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  {
   "id": 7,
   "question": "What are the top 5 most frequently copy number altered genes in the Osteosarcoma study from TARGET?",
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   "mismatch": [],
   "a": {
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   "delta": 100.0,
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  {
   "id": 22,
   "question": "Do patients with PIK3CA mutations have different overall survival outcomes compared to PIK3CA wild-type patients in breast cancer from the MSK-CHORD Study?",
   "category": "Survival & outcomes",
   "track": "analysis",
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  {
   "id": 69,
   "question": "Which patients have a TP53 G199V mutation? Which are somatic vs germline?",
   "category": "Patient & sample lookup",
   "track": "data",
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    "p90_latency_all": 16.19073629193008,
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    "fast_share_all": 0.0,
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  {
   "id": 70,
   "question": "In MSS colorectal cancer, what is the frequency of BRAF oncogenic mutations (as defined by OncoKB)? Use the 2017 MSK study for this. Can you give me a table of all these mutations, with frequency, count and denominator?",
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  {
   "id": 71,
   "question": "What is the current and future support for storing and analyzing germline variants in cBioPortal, compared to other alternatives?",
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   "track": "out_of_scope",
   "gradeable": true,
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   "id": 72,
   "question": "Is there any study with a polygenic risk score?",
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   "gradeable": true,
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  {
   "id": 75,
   "question": "How many patients have a shallow deletion for SMARCA4 in the POG study?",
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   "a": {
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   "b": {
    "expected": 1,
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  {
   "id": 77,
   "question": "can you show me the minerva viewer for the ohsu htan sample",
   "category": "Patient & sample lookup",
   "track": "navigation",
   "gradeable": true,
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   "a": {
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    "p90_latency_all": 23.082301249960437,
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   "b": {
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  {
   "id": 80,
   "question": "Is there a cohort of NSCLC patient samples that have Kras mutations, wild-type p53, and high expression levels of c-Myc?",
   "category": "Patient & sample lookup",
   "track": "data",
   "gradeable": true,
   "mismatch": [],
   "a": {
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   "b": {
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  {
   "id": 82,
   "question": "How many GLASS patients developed hypermutation after TMZ treatment?",
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   "a": {
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  {
   "id": 85,
   "question": "generate a oncoprint of kras, stk11, keap1, tp53 alterations stratified by smoking status in lung adenocarcinoma from the mskcc clincogenomic sequencing cohort. Please only select oncogenic somatic alterations and remove samples with unknown smoking status",
   "category": "Alteration frequency",
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   "id": 88,
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   "id": 89,
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   "question": "Can you help me write a production-ready Python script using Bokeh to build an interactive clinicogenomic dashboard to analyzing the MSK-CHORD dataset? I have some specific requirements I can give you",
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  {
   "id": 100,
   "question": "How many samples are there that have any of these mutations in SEPHS1: p.Arg371Trp, p.Arg371Gln, p.Arg371Gly?",
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   "track": "data",
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   "id": 101,
   "question": "List the top 20 mutated genes in study nbl_msk_2023.",
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  {
   "id": 103,
   "question": "in salivary cancer (adenoid cystic carcinoma), what are the expected drivers ? Classify them by actionability. What about BCOR mutations, either somatic or germline ?",
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   "track": "data",
   "gradeable": true,
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  {
   "id": 104,
   "question": "write me python code that can query the timeline files for msk-chord",
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   "track": "out_of_scope",
   "gradeable": true,
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    "expected": 1,
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  {
   "id": 105,
   "question": "list the portal studies for pediatric cancers that were published in the last 5 years",
   "category": "Study discovery",
   "track": "data",
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  {
   "id": 106,
   "question": "Which studies have RNA expression for renal cancer?",
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    "expected": 1,
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  {
   "id": 110,
   "question": "Can you explore the difference in mutation frequency between left-sided and right-sided CRC?",
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   "track": "analysis",
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   "a": {
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  {
   "id": 111,
   "question": "can you show me a study with longitudinal data and a patient that has multiple samples over time?",
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   "track": "navigation",
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   "b": {
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   "id": 136,
   "question": "In the TCGA Breast Cancer study, do TP53 mutations and high MYC expression co-occur or are they mutually exclusive?",
   "category": "Co-occurrence & exclusivity",
   "track": "analysis",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
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    "fast_share_all": 0.0,
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    "tool_error_rate": 10.0,
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   "b": {
    "expected": 1,
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  {
   "id": 138,
   "question": "show me all KRAS mutations in colorectal cancer that are not at position 12",
   "category": "Variants & hotspots",
   "track": "navigation",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
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    "fast_share_all": 0.0,
    "mean_llm_calls": 9,
    "median_llm_calls": 9,
    "mean_tool_rounds": 0,
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   "b": {
    "expected": 1,
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    "p90_latency_all": 25.829602333018556,
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    "fast_share_all": 0.0,
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   },
   "delta": 0.0,
   "latency_delta": -3.9749054999556392,
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  {
   "id": 139,
   "question": "show me cholangio with idh1 mutations other than r132",
   "category": "Variants & hotspots",
   "track": "navigation",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
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    "unexpected": 0,
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    "attempt_rate": 100.0,
    "pass_rate": 0.0,
    "median_latency": 51.75310091697611,
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    "fast_share_all": 0.0,
    "mean_llm_calls": 17,
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    "tool_error_rate": 0.0,
    "cost_per_answer": 0.1289756,
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   "b": {
    "expected": 1,
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    "p90_latency_all": 26.742988584097475,
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    "mean_llm_calls": 9,
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   },
   "delta": 0.0,
   "latency_delta": -25.010112332878634,
   "verdict": "same"
  },
  {
   "id": 140,
   "question": "what's the frequency of different idh1 mutations in glioma vs cholangio vs chndrosarcoma? Give me a link to compare the frequency of the specific IDH1 mutations in those cancer types.",
   "category": "Variants & hotspots",
   "track": "navigation",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
    "completed": 1,
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    "eligible": 1,
    "unexpected": 0,
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    "median_latency": 62.84515754203312,
    "p90_latency": 62.84515754203312,
    "median_latency_all": 62.84515754203312,
    "p90_latency_all": 62.84515754203312,
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    "fast_share_all": 0.0,
    "mean_llm_calls": 12,
    "median_llm_calls": 12,
    "mean_tool_rounds": 0,
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   "b": {
    "expected": 1,
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    "p90_latency": 42.9717679170426,
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    "p90_latency_all": 42.9717679170426,
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    "routed_to": [],
    "icons": "✗"
   },
   "delta": 0.0,
   "latency_delta": -19.873389624990523,
   "verdict": "same"
  },
  {
   "id": 141,
   "question": "is there a relatinoship between mgmt methylation and idh1 mutation in glioma?",
   "category": "Expression & multi-omics",
   "track": "analysis",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
    "completed": 1,
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    "unexpected": 0,
    "recall": 100.0,
    "precision": 100.0,
    "attempt_rate": 100.0,
    "pass_rate": 100.0,
    "median_latency": 111.15956991701387,
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    "fast_share_all": 0.0,
    "mean_llm_calls": 29,
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    "routed_to": [],
    "icons": "✓"
   },
   "b": {
    "expected": 1,
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   "delta": 0.0,
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  },
  {
   "id": 142,
   "question": "Give me an OncoPrint for RTK genes in lung cancer, limited to driver events.",
   "category": "Alteration frequency",
   "track": "navigation",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
    "completed": 1,
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    "unexpected": 0,
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    "attempt_rate": 100.0,
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    "fast_share_all": 0.0,
    "mean_llm_calls": 3,
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    "tool_error_rate": 0.0,
    "cost_per_answer": 0.019287150000000003,
    "latency_stdev": null,
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    "icons": "✗"
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   "b": {
    "expected": 1,
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    "p90_latency": 12.55894554196857,
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    "p90_latency_all": 12.55894554196857,
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   },
   "delta": 0.0,
   "latency_delta": 0.30862587597221136,
   "verdict": "same"
  },
  {
   "id": 143,
   "question": "show me P135L mutations in $p14^{ARF}$",
   "category": "Variants & hotspots",
   "track": "navigation",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
    "completed": 1,
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    "passes": 1,
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    "eligible": 1,
    "unexpected": 0,
    "recall": 100.0,
    "precision": 100.0,
    "attempt_rate": 100.0,
    "pass_rate": 100.0,
    "median_latency": 17.65531670791097,
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    "median_latency_all": 17.65531670791097,
    "p90_latency_all": 17.65531670791097,
    "fast_share": 0.0,
    "fast_share_all": 0.0,
    "mean_llm_calls": 5,
    "median_llm_calls": 5,
    "mean_tool_rounds": 0,
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    "failed_handoffs": 0,
    "tool_error_rate": 0.0,
    "cost_per_answer": 0.04190215,
    "latency_stdev": null,
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    "flaky": false,
    "routed_to": [],
    "icons": "✓"
   },
   "b": {
    "expected": 1,
    "completed": 1,
    "failed": 0,
    "missing": 0,
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    "unexpected": 0,
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    "precision": 100.0,
    "attempt_rate": 100.0,
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    "median_latency": 32.01869891700335,
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    "p90_latency_all": 32.01869891700335,
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    "cost_per_answer": 0.053001150000000004,
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   },
   "delta": 0.0,
   "latency_delta": 14.363382209092379,
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  },
  {
   "id": 144,
   "question": "are lung carcinosarcomas associated with BRIP1 mutations?",
   "category": "Alteration frequency",
   "track": "navigation",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
    "completed": 1,
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    "unexpected": 0,
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    "attempt_rate": 100.0,
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    "mean_llm_calls": 18,
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    "tool_error_rate": 4.761904761904762,
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   "b": {
    "expected": 1,
    "completed": 1,
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    "p90_latency_all": 16.331552208168432,
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   "delta": 0.0,
   "latency_delta": -60.63461299985647,
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  },
  {
   "id": 145,
   "question": "Which genes are enriched for mutations between NSCLC vs squamous cell carcinoma?",
   "category": "Alteration frequency",
   "track": "analysis",
   "gradeable": true,
   "mismatch": [],
   "a": {
    "expected": 1,
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   "b": {
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   "delta": 0.0,
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 "question_verdicts": {
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  "worse": 27,
  "same": 104
 }
}
