• 00:11 1.
    index 1
  • 01:57 2.
    Mutation
  • 01:25 3.
    Mutation
  • 01:45 4.
    Nomenclature for RefSeq Accession Number
  • 01:02 5.
    BeadChip Products
  • 00:54 6.
    Characters Used for Describing Seq. Variants
  • 00:52 7.
    Question
  • 04:02 8.
    Characters Used for Describing Seq. Variants
  • 02:25 9.
    Characters Used for Describing Seq. Variants
  • 03:01 10.
    Characters Used for Describing Seq. Variants
  • 02:59 11.
    Examples for Description of Sequence Variants
  • 01:34 12.
    Examples for Description of Sequence Variants
  • 03:20 13.
    Structural Variants
  • 01:44 14.
    Single Nucleotide Polymorphism1
  • 00:31 15.
    Basic Concept of SNPs
  • 01:17 16.
    Single Nucleotide Polymorphism2
  • 00:31 17.
    Phenotype Associated With SNP
  • 02:05 18.
    Mendelian vs. Complex Disease
  • 01:23 19.
    Common Variant vs. Multiple Rare Variant Hypothesis
  • 02:17 20.
    Approaches to Gene Mapping
  • 01:50 21.
    Linkage and Linkage Disequilibrium
  • 01:23 22.
    Association Studies and Linkage Disequilibrium
  • 02:12 23.
    Linkage Disequilibrium1
  • 01:20 24.
    Linkage Disequilibrium2
  • 02:33 25.
    Tag SNP
  • 00:28 26.
    dbSNPhttps://www.ncbi.nlm.nih.gov/snp
  • 01:40 27.
    Genotype-Tissue Expression (GTEx)
  • 01:51 28.
    Summary of Identifying Genetic Variation
  • 01:11 29.
    Haplotype
  • 01:10 30.
    Genome Phasing
  • 01:25 31.
    Loss of Heterozygosity (LOH)
  • 00:53 32.
    Loss of Heterozygosity (LOH)
  • 02:36 33.
    Genome-Wide Association Study (GWAS)
  • 01:04 34.
    Clinical Translation of Findings From Genome-Wide Association Studies
  • 02:26 35.
    Affymetrix Genotyping Assay
  • 00:21 36.
    Illumina Genotyping Beadchip
  • 02:00 37.
    Golden Gate Assay
  • 00:29 38.
    Golden Gate Assay
  • 01:43 39.
    Infinium II Assay
  • 00:57 40.
    Sequenom MassARRAY iPLEX Platform
  • 00:38 41.
    Digital PCR
  • 01:09 42.
    Pyrosequencing – SNP and Mutation Analysis
  • 02:54 43.
    Exome Sequencing
  • 01:56 44.
    Data Analysis and Computation
  • 00:48 45.
    Resources & Software Tools
  • 02:20 46.
    Resources & Software Tools
  • 00:26 47.
    Resources & Software Tools
  • 00:38 48.
    Question
  • 02:56 49.
    Nomenclature of Cytogenetic Band
  • 00:59 50.
    Structural Variants
  • 01:32 51.
    Influence of Structural Variants on Phenotype
  • 02:48 52.
    Mutation
  • 01:09 53.
    Nondisjunction
  • 00:04 54.
    Question
  • 01:20 55.
    Mosaicism
  • 00:45 56.
    Chromothripsis / Kataegis
  • Index
  • Notes
  • Comment
  • Fullscreen
Genomic approaches to study DNA structure variation (0427)
Duration: 1:27:36, Browse: 582, Last Updated: 2021-05-05
    • 00:11 1.
      index 1
    • 01:57 2.
      Mutation
    • 01:25 3.
      Mutation
    • 01:45 4.
      Nomenclature for RefSeq Accession Number
    • 01:02 5.
      BeadChip Products
    • 00:54 6.
      Characters Used for Describing Seq. Variants
    • 00:52 7.
      Question
    • 04:02 8.
      Characters Used for Describing Seq. Variants
    • 02:25 9.
      Characters Used for Describing Seq. Variants
    • 03:01 10.
      Characters Used for Describing Seq. Variants
    • 02:59 11.
      Examples for Description of Sequence Variants
    • 01:34 12.
      Examples for Description of Sequence Variants
    • 03:20 13.
      Structural Variants
    • 01:44 14.
      Single Nucleotide Polymorphism1
    • 00:31 15.
      Basic Concept of SNPs
    • 01:17 16.
      Single Nucleotide Polymorphism2
    • 00:31 17.
      Phenotype Associated With SNP
    • 02:05 18.
      Mendelian vs. Complex Disease
    • 01:23 19.
      Common Variant vs. Multiple Rare Variant Hypothesis
    • 02:17 20.
      Approaches to Gene Mapping
    • 01:50 21.
      Linkage and Linkage Disequilibrium
    • 01:23 22.
      Association Studies and Linkage Disequilibrium
    • 02:12 23.
      Linkage Disequilibrium1
    • 01:20 24.
      Linkage Disequilibrium2
    • 02:33 25.
      Tag SNP
    • 00:28 26.
      dbSNPhttps://www.ncbi.nlm.nih.gov/snp
    • 01:40 27.
      Genotype-Tissue Expression (GTEx)
    • 01:51 28.
      Summary of Identifying Genetic Variation
    • 01:11 29.
      Haplotype
    • 01:10 30.
      Genome Phasing
    • 01:25 31.
      Loss of Heterozygosity (LOH)
    • 00:53 32.
      Loss of Heterozygosity (LOH)
    • 02:36 33.
      Genome-Wide Association Study (GWAS)
    • 01:04 34.
      Clinical Translation of Findings From Genome-Wide Association Studies
    • 02:26 35.
      Affymetrix Genotyping Assay
    • 00:21 36.
      Illumina Genotyping Beadchip
    • 02:00 37.
      Golden Gate Assay
    • 00:29 38.
      Golden Gate Assay
    • 01:43 39.
      Infinium II Assay
    • 00:57 40.
      Sequenom MassARRAY iPLEX Platform
    • 00:38 41.
      Digital PCR
    • 01:09 42.
      Pyrosequencing – SNP and Mutation Analysis
    • 02:54 43.
      Exome Sequencing
    • 01:56 44.
      Data Analysis and Computation
    • 00:48 45.
      Resources & Software Tools
    • 02:20 46.
      Resources & Software Tools
    • 00:26 47.
      Resources & Software Tools
    • 00:38 48.
      Question
    • 02:56 49.
      Nomenclature of Cytogenetic Band
    • 00:59 50.
      Structural Variants
    • 01:32 51.
      Influence of Structural Variants on Phenotype
    • 02:48 52.
      Mutation
    • 01:09 53.
      Nondisjunction
    • 00:04 54.
      Question
    • 01:20 55.
      Mosaicism
    • 00:45 56.
      Chromothripsis / Kataegis
    Location
    Folder name
    2021
    Author
    賴亮全
    Branch
    賴亮全教授
    Created
    2021-04-27 16:10:11
    Last Updated
    2021-05-05 12:27:40
    Browse
    582
    Duration
    1:27:36