Book Cover
Streaming video
Author Carter, Nigel P., (The Wellcome Trust Sanger Institute, UK), speaker

Title Array comparative genomic hybridisation to characterise copy number variation in the human genome / Nigel P. Carter
Published London : Henry Stewart Talks, 2009
Online access available from:
Henry Stewart Talks: Biomedical & Life Sciences Lectures    View Resource Record  

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Description 1 online resource (1 streaming video file (17 min.) : color, sound)
Series 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
Contents 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
Notes Animated audio-visual presentation with synchonized narration
Title from title frames
Mode of access: World Wide Web
System requirements: Browser compatibility: updated Mozilla Firefox, Google Chrome, Safari or Internet Explorer 8+. Browser settings: enable JavaScript, enable cookies from the Henry Stewart Talks site. Required Desktop Browser plugins & viewers: Updated Adobe Flash Player & Adobe Acrobat Reader. Mobile device & operating system versions: Android v4.0+, iPhone 4+ (iOS v6.x+), iPad 2+ (iOS v6.x+), BlackBerry OS v7.0+, Windows Phone v6.5.1+
Subject Gene Dosage.
Genetic Variation.
Genome, Human.
Oligonucleotide Array Sequence Analysis.
Genre/Form Video recordings.
Form Streaming video
Other Titles Array comparative genomic hybridization to characterize copy number variation in the human genome