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4,299,418 works, Canadian by any of four routes.

Every filter state is a URL; the URL is the query; the query is citable via /q/⟨hash⟩. The page, the API and the export parse the same parameters.

The current cohort, streamed from the database: every work column, the machine labels, the provisional scores, and the per-row validation status. Exports are capped at 100,000 rows. Mints a permanent /q/ link for this exact query. The same filters always produce the same link, whoever asks.

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Genomics and Rare Diseases
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Direct Codex and Gemma labels are unvalidated and sparse. Distilled predictions cover the full frame and are also unvalidated. Choose the evidence source explicitly; absence of a direct label is never a negative label.

affaffiliation
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The four routes compose: require the funder route and exclude affiliation to get the funder-only stratum no affiliation-based frame ever sees.

1,801 results · 1 filter active ·
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20002025
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Machine labels · sparse coverage
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An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
1,801 works in the cohort · of 4,299,418page 8 of 37

Labels cover 4 of 1,801 works in this cohort. The rest are unlabeled, which is not a negative label: the label table is sparse today and grows as labeling rounds land.

Distilled predictions cover 1,801 of 1,801 works in this cohort. Predictions are machine_predicted_unvalidated teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundunlabeled
CooVar: Co-occurring variant analyzer
Ismael A. Vergara, Christian Frech, Nansheng Chen
2012· article· en· BMC Research Notes· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
39
citations
affunlabeled
FDA Patient-Focused Drug Development Guidances
Anne T. Berg, Natasha N. Ludwig, Mary Wojnaroski, Chere A. T. Chapman, Rebecca Hommer, Gabrielle Conecker +2 more
2023· article· en· Neurology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
36
citations
affno abstractunlabeled
Inferring compound heterozygosity from large-scale exome sequencing data
Michael H. Guo, Laurent C. Francioli, Sarah L. Stenton, Julia K. Goodrich, Nicholas A. Watts, Moriel Singer‐Berk +221 more
2023· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
35
citations
afffundaboutunlabeled
<i>SETD1B</i>-associated neurodevelopmental disorder
Alexandra Roston, Dan Evans, Harinder Gill, Margaret L. McKinnon, Bertrand Isidor, Benjamin Cogné +8 more
2020· article· en· Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
35
citations
afffundunlabeled
A generalizable pre-clinical research approach for orphan disease therapy
Chandree L. Beaulieu, Mark E. Samuels, Sean Ekins, Christopher R. McMaster, A.M. Edwards, Adrian R. Krainer +4 more
2012· review· en· Orphanet Journal of Rare Diseases· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
34
citations
afffundunlabeled
Rare deleterious germline variants and risk of lung cancer
Yanhong Liu, Jun Xia, James McKay, Spiridon Tsavachidis, Xiangjun Xiao, Margaret R. Spitz +41 more
2021· article· en· npj Precision Oncology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
32
citations

How this was built: Screen · Findings · About