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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.

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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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Genomic variations and chromosomal abnormalities
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Abstract
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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.

1,322 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.
1,322 works in the cohort · of 4,299,418page 13 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 teacher distillation outputs. Candidate is the union; consensus is the intersection.

afffundno abstractunlabeled
DNA methylation episignature in Gabriele-de Vries syndrome
Florian Cherik, Jack Reilly, Jennifer Kerkhof, Michael A. Levy, Haley McConkey, Mouna Barat‐Houari +28 more
2022· article· en· Genetics in Medicine· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
17
citations
affunlabeled
Resources for Genetic Variation Studies
David Serre, Thomas J. Hudson
2006· review· en· Annual Review of Genomics and Human Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · metaepi_narrowconsensus · none
17
citations
fundno affunlabeled
Simple Method for Preparation of Fluor/Hapten-Labeled dUTP
Manjunath Nimmakayalu, Octavian Henegariu, David C. Ward, Patricia Bray‐Ward
2000· article· en· BioTechniques· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
17
citations
affunlabeled
Analphoid 3qter markers
Ikuko Teshima, Erawati V. Bawle, Rosanna Weksberg, Cheryl Shuman, Daniel L. Van Dyke, Stuart Schwartz
2000· article· en· American Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · insufficient_payloadconsensus · none
16
citations
fundno affno abstractunlabeled
A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features – Is cardiac assessment necessary for all patients with 17p13.3 microduplication?
Alvin Chi Chung Ho, Anthony P. Y. Liu, Kin Shing Lun, Wing‐Fai Tang, Kelvin Y.K. Chan, Elizabeth Y.T. Lau +3 more
2012· article· en· European Journal of Medical Genetics· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
16
citations
afffundunlabeled
Rare germline copy number variants (CNVs) and breast cancer risk
Joe Dennis, Jonathan P. Tyrer, Logan C. Walker, Kyriaki Michailidou, Leila Dorling, Manjeet K. Bolla +137 more
2022· article· en· Communications Biology· Biochemistry, Genetics and Molecular Biology
distilled prediction:candidate · noneconsensus · none
15
citations
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