Widespread structural variations in the human genome [electronic resource] / Charles Lee.
Material type:
FilmSeries: Henry Stewart talksBiomedical & life sciences collection. Using bioinformatics in the exploration of genetic diversity : fundamentals and recent advances: Publisher: London : Henry Stewart Talks, 2007Description: 1 online resource (1 streaming video file (59 min.) : color, sound)Subject(s): Computational Biology | Genetics | Genome, Human | Variation (Genetics)Online resources: Click here to access online | Series Animated audio-visual presentation with synchronized narration.
Title from title frames.
Contents: Genetic differences and similarities between normal individuals -- Single Nucleotide Polymorphisms (SNPs) -- Structural variants in the human genome -- Comparative Genomic Hybridization (CGH) -- Clinical genetic diagnostics -- Copy Number Variation (CNV) -- Overlapping -- Large-scale variation -- CNVs in the human genome is probably underestimated -- Fine-scale structural variation of the human genome -- In silico computational strategy -- Holes in the human genome -- Common deletion polymorphisms -- International HapMap Project -- Genotyping failures -- Common/complex diseases -- Gene expression -- Implications of CNVs to genetic diagnostics -- Toward a global CNV map for the human genome -- Copy Number Variation Project -- CNVs in other mammalian species.
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Mode of access: World Wide Web.