MétaCan
Menu
Cohort builder

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.

Search term
Author
Year range
Sort
Language
Type
Field
Venue
Topic
Genomic variations and chromosomal abnormalities
Retraction
Abstract
Evidence source
Study design
Label agreement
Label status

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
fundfunder
venuejournal
aboutaboutness

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

1,322 results · 1 filter active ·
Results by year
20002025
Publication date
Categories
Machine labels · sparse coverage
Evidence
Language
Type
Citations
An unlabeled work is unknown, not a negative. Label coverage is reported on every query.
1,322 works in the cohort · of 4,299,418page 18 of 27

Labels cover 3 of 1,322 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 1,322 of 1,322 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.

affunlabeled
Phenotypic manifestation in a child with 46,X,der(X)t(X;1)(q24;q31.1)
Kelly A. Collins, Patrice Eydoux, Alessandra M.V. Duncan, June Ortenberg, Kenneth Silver, Vazken M. Der Kaloustian
2000· article· en· American Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
5
citations
affunlabeled
Microarray CGH
Ben Beheshti, Paul C. Park, Ilan Braude, Jeremy A. Squire
2003· article· en· Molecular Cytogenetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
5
citations
affunlabeled
Human chromosome mapping of single copy genes
Barbara Beatty, Stephen W. Scherer
2002· book-chapter· en· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
5
citations
affunlabeled
Array CGH in Brain Tumors
Gayatry Mohapatra, Julia Sharma, Stephen Yip
2013· article· en· Methods in molecular biology· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
5
citations
affno abstractunlabeled
A note on the single genotype resolution problem
Hao Lin, Ze-Feng Zhang, Qiangfeng Cliff Zhang, Dongbo Bu, Ming Li
2004· article· en· Journal of Computer Science and Technology· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
5
citations
affunlabeled
Bioinformatics in Neurosurgery
Michael D. Taylor, Todd G. Mainprize, James T. Rutka
2003· article· en· Neurosurgery· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
5
citations
afffundunlabeled
Human copy number variants are enriched in regions of low mappability
Jean Monlong, Patrick Cossette, Caroline Meloche, Guy A. Rouleau, Simon Girard, Guillaume Bourque
2015· preprint· en· bioRxiv (Cold Spring Harbor Laboratory)· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
4
citations
venueno affno abstractunlabeled
Ocular manifestations in Koolen–de Vries syndrome: an international study
D. Shalev, David A. Koolen, Bert de Vries, Sharon Blum Meirovitch, Jean‐Louis Mandel, Pauline Burger +3 more
2023· article· en· Canadian Journal of Ophthalmology· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
4
citations
affno abstractunlabeled
Genetic mechanisms of neurodevelopmental disorders
Ping Yee Billie Au, Alison Eaton, David A. Dyment
2020· book-chapter· en· Handbook of clinical neurology· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
4
citations
affno abstractunlabeled
Trisomy of Chromosome 10 in Two Cases of Ovarian Carcinoma
Jia‐Chi Wang, Anne‐Marie Mes‐Masson, Patricia N. Tonin, Diane Provencher, Patrice Eydoux
2000· article· en· Cancer Genetics and Cytogenetics· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
4
citations
affunlabeled
Duplication 2p16 is associated with perisylvian polymicrogyria
Dina Amrom, Annapurna Poduri, Jennifer S. Goldman, Bernard Dan, Nicolas Deconinck, Bruno Pichon +5 more
2019· article· en· American Journal of Medical Genetics Part A· Biochemistry, Genetics and Molecular Biology
machine prediction:candidate · noneconsensus · none
4
citations

How this was built: Screen · Findings · About