The future of CNVs [electronic resource] : sequence based resolution and links to human disease, (part 2 of 2) / Evan Eichler.
Material type:
FilmSeries: Henry Stewart talksBiomedical & life sciences collection. Biomarkers: ; Henry Stewart talksBiomedical & life sciences collection. Copy number variation: Publisher: London : Henry Stewart Talks, 2017Description: 1 online resource (1 streaming video file (31 min.) : color, sound)Other title: Future of CNVs : sequence based resolution and links to human disease. Part 2 | Sequence based resolution and links to human disease 2Subject(s): Biochemical markers | Human genetics | Medical genetics | Nucleotide sequence | Variation (Biology) | Biomarkers | Chromosome Inversion | Chromosomes, Human, Pair 17 -- genetics | DNA Copy Number Variations | Gene Dosage | Genetic Variation -- genetics | Genetics, Medical | Genome, Human | Genomics -- trends | Genotyping Techniques | High-Throughput Nucleotide Sequencing | Molecular Sequence Data | Sequence Analysis, DNA -- methods | Sequence Deletion | Sequence InversionOnline resources: Click here to access online | Series (Copy number variation) | Series (Biomarkers) Animated audio-visual presentation with synchronized narration.
Title from title frames.
Contents: Future discovery of CNVs -- Genotyping -- Inversion and deletion -- 17q21.31 targeted sequencing -- Application of next-generation sequencing technology -- Personalized duplication or CNV map -- Long read sequencing technology -- Single-molecule, real-time detection of structural variation (SMRT-SV) -- Full-spectrum of human genetic variation.
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Mode of access: World Wide Web.