Copy number variation in association studies of human disease [electronic resource] / Steven McCarroll.
Material type: FilmSeries: Henry Stewart talksBiomedical & life sciences collection. Copy number variation: Publisher: London : Henry Stewart Talks, 2009Description: 1 online resource (1 streaming video file (41 min.) : color, sound)Subject(s): Gene Dosage | Genetic Predisposition to Disease | Genetic VariationOnline resources: Click here to access online | SeriesAnimated audio-visual presentation with synchonized narration.
Title from title frames.
Contents: Why study CNV in human disease? -- Population genetics of human CNV -- Low copy sequences -- Medium-to-large CNVs -- Inheritance vs. de novo mutation -- Common CNV regions -- Rare and common variants -- Most common CNPs are in LD with SNPs -- Haplotype sharing -- GWAS -- Association frameworks for analyzing CNVs -- Data quality in CNV studies -- Interpreting CNV-disease association findings.
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Mode of access: World Wide Web.