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The future of CNVs : sequence based resolution and links to human disease, (part 2 of 2) / Evan Eichler.
- Format:
- Video
- Author/Creator:
- Eichler, Evan (University of Washington, USA), Speaker.
- Series:
- Henry Stewart talks. Biomedical & life sciences collection. Biomarkers.
- Henry Stewart talks. Biomedical & life sciences collection. Copy number variation.
- Biomarkers : the path forward to highly sensitive and specific molecular diagnostics, 2056-452X
- Copy number variation : expanding the repertoire of genetic alterations in studies of natural variation and disease, 2056-452X
- Language:
- English
- Subjects (All):
- 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 Inversion.
- Medical Subjects:
- 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 Inversion.
- Genre:
- Video recordings.
- Physical Description:
- 1 online resource (1 streaming video file (31 min.)) : color, sound.
- polychrome
- Other Title:
- Future of CNVs : sequence based resolution and links to human disease. Part 2
- Sequence based resolution and links to human disease 2
- Place of Publication:
- London : Henry Stewart Talks, 2017.
- System Details:
- Mode of access: World Wide Web.
- video file
- Contents:
- 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.
- Notes:
- Animated audio-visual presentation with synchronized narration.
- Title from title frames.
- Publisher Number:
- 4454 Henry Stewart Talks
- Access Restriction:
- Restricted for use by site license.
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