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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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Nature Genetics
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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.

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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.

943 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.
943 works in the cohort · of 4,299,418page 1 of 19

Labels cover 4 of 943 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 943 of 943 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.

afffundno abstractunlabeled
A reference panel of 64,976 haplotypes for genotype imputation
Richard Durbin, Klaudia Walter, Yang Luo, Shane McCarthy, Nicole Soranzo, Jeffrey C. Barrett +72 more
2016· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
3,273
citations
affno abstractunlabeled
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
Marianne Abifadel, Mathilde Varret, Jean‐Pierre Rabès, Delphine Allard, Khadija Ouguerram, Martine Devillers +20 more
2003· article· en· Nature Genetics· Medicine
machine prediction:candidate · noneconsensus · none
3,011
citations
affno abstractunlabeled
Detection of large-scale variation in the human genome
A. John Iafrate, Lars Feuk, Miguel N. Rivera, Marc Listewnik, Patricia K. Donahoe, Ying Qi +2 more
2004· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
2,910
citations
affno abstractunlabeled
The genome of the mesopolyploid crop species Brassica rapa
Xiaowu Wang, Hanzhong Wang, Jun Wang, Rifei Sun, Jian Wu, Shengyi Liu +102 more
2011· article· en· Nature Genetics· Agricultural and Biological Sciences
machine prediction:candidate · noneconsensus · none
2,205
citations
affno abstractunlabeled
High-resolution haplotype structure in the human genome
Mark J. Daly, John D. Rioux, S. F. Schaffner, Thomas J. Hudson, Eric S. Lander
2001· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
1,724
citations
afffundno abstractunlabeled
An atlas of genetic influences on human blood metabolites
So–Youn Shin, Eric B. Fauman, Ann-Kristin Petersen, Jan Krumsiek, Rita Santos, Jie Huang +29 more
2014· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
1,645
citations
fundno affno abstractunlabeled
A copy number variation morbidity map of developmental delay
Gregory M. Cooper, Bradley P. Coe, Santhosh Girirajan, Jill A. Rosenfeld, Tiffany Vu, Carl Baker +20 more
2011· article· en· Nature Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
1,404
citations
fundno affno abstractunlabeled
Most genetic risk for autism resides with common variation
Trent Gaugler, Lambertus Klei, Stephan Sanders, Corneliu Bodea, Arthur P. Goldberg, Ann B. Lee +13 more
2014· article· en· Nature Genetics· Neuroscience
machine prediction:candidate · noneconsensus · none
1,286
citations

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