Carter, Nigel P.,

Array comparative genomic hybridisation to characterise copy number variation in the human genome [electronic resource] / Array comparative genomic hybridization to characterize copy number variation in the human genome Nigel P. Carter. - London : Henry Stewart Talks, 2009. - 1 online resource (1 streaming video file (17 min.) : color, sound). - Copy number variation : expanding the repertoire of genetic alterations in studies of natural variation and disease, 2056-452X . - Henry Stewart talks. Biomedical & life sciences collection. Copy number variation. .

Animated audio-visual presentation with synchonized narration. Title from title frames.

Contents: Array Comparative Hybridization (array-CGH) and measurement of copy number -- Development of array-CGH technology from convention CGH on metaphase chromosomes -- Initial use for identifying copy number changes in tumors -- Identification of normal copy number variation -- Increasing resolution of array-CGH reveals the scope, complexity and importance of normal copy number variation.

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Mode of access: World Wide Web.

2146 Henry Stewart Talks


Gene Dosage.
Genetic Variation.
Genome, Human.
Oligonucleotide Array Sequence Analysis.
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