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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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venuejournal
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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 32 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. The Gemma side is a direct model label for every work (title-only); the Codex side is a distilled, calibrated classifier. Candidate is the union; consensus is the intersection.

venueno affno abstractunlabeled
10.1016/s1541-9800(13)70036-x
2000· article· en· Time to knit· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · insufficient_payloadconsensus · insufficient_payload
0
citations
venueno affno abstractunlabeled
10.1016/s0246-0378(19)30424-5
2000· article· en· Time to knit· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · insufficient_payloadconsensus · insufficient_payload
0
citations
fundno affunlabeled
Refinement of genetic variants needs attention
Omar Abdelwahab, Davoud Torkamaneh
2024· preprint· en· arXiv (Cornell University)· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
0
citations
affno abstractunlabeled
UNC93B1 Deficiency
Henry Y. Lu, Stuart E. Turvey
2018· book-chapter· en· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
0
citations
affno abstractunlabeled
Genetische Diagnostik
Karl Martin Klein, Philipp S. Reif
2020· book-chapter· de· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
0
citations
fundno affunlabeled
10 years of research on rare diseases
Thierry Damerval
2023· other· fr· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · bibliometricsconsensus · none
0
citations
venueno affunlabeled
P.053 Biallelic SCN1A variants with divergent epilepsy phenotypes
Rebecca D. Pentz, R Hough, Chumei Li, Mark A. Tarnopolsky, Kevin Jones, Rajesh Ramachandran Nair +1 more
2025· article· en· Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
0
citations

How this was built: Screen · Findings · About