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Origins and functional impact of copy number variation in the human genome
Why is this work in the frame?
A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.
Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.
Abstract
No abstract. This is not a gap in this database — OpenAlex has none either. 23.3% of the frame is in this state, and the screen finds HALF as much metaresearch here, so the absence is a measured bias rather than a missing field.
The record
- Venue
- Nature
- Topic
- Genomic variations and chromosomal abnormalities
- Field
- Biochemistry, Genetics and Molecular Biology
- Canadian institutions
- University of TorontoHospital for Sick Children
- Funders
- National Human Genome Research InstituteCanadian Institutes of Health ResearchNational Institute of General Medical SciencesNederlandse Organisatie voor Wetenschappelijk OnderzoekWellcome Trust
- Keywords
- Copy-number variationGeneticsBiologyInternational HapMap ProjectHuman genomeSingle-nucleotide polymorphismLinkage disequilibriumGenomeGenome-wide association study1000 Genomes ProjectStructural variationLocus (genetics)GenomicsGenotypeGene
- Has abstract in OpenAlex
- no