• 00:00 1.
    index 1
  • 00:11 2.
    Mutation
  • 02:08 3.
    Mutation
  • 03:34 4.
    Nomenclature for RefSeq Accession Number
  • 05:19 5.
    BeadChip Products
  • 06:21 6.
    Characters Used for Describing Seq. Variants
  • 07:16 7.
    Question
  • 08:08 8.
    Characters Used for Describing Seq. Variants
  • 12:11 9.
    Characters Used for Describing Seq. Variants
  • 14:36 10.
    Characters Used for Describing Seq. Variants
  • 17:38 11.
    Examples for Description of Sequence Variants
  • 20:37 12.
    Examples for Description of Sequence Variants
  • 22:12 13.
    Structural Variants
  • 25:32 14.
    Single Nucleotide Polymorphism1
  • 27:17 15.
    Basic Concept of SNPs
  • 27:48 16.
    Single Nucleotide Polymorphism2
  • 29:05 17.
    Phenotype Associated With SNP
  • 29:37 18.
    Mendelian vs. Complex Disease
  • 31:43 19.
    Common Variant vs. Multiple Rare Variant Hypothesis
  • 33:06 20.
    Approaches to Gene Mapping
  • 35:24 21.
    Linkage and Linkage Disequilibrium
  • 37:15 22.
    Association Studies and Linkage Disequilibrium
  • 38:38 23.
    Linkage Disequilibrium1
  • 40:50 24.
    Linkage Disequilibrium2
  • 42:11 25.
    Tag SNP
  • 44:45 26.
    dbSNPhttps://www.ncbi.nlm.nih.gov/snp
  • 45:13 27.
    Genotype-Tissue Expression (GTEx)
  • 46:53 28.
    Summary of Identifying Genetic Variation
  • 48:44 29.
    Haplotype
  • 49:56 30.
    Genome Phasing
  • 51:07 31.
    Loss of Heterozygosity (LOH)
  • 52:32 32.
    Loss of Heterozygosity (LOH)
  • 53:26 33.
    Genome-Wide Association Study (GWAS)
  • 56:02 34.
    Clinical Translation of Findings From Genome-Wide Association Studies
  • 57:06 35.
    Affymetrix Genotyping Assay
  • 59:32 36.
    Illumina Genotyping Beadchip
  • 59:54 37.
    Golden Gate Assay
  • 1:01:54 38.
    Golden Gate Assay
  • 1:02:24 39.
    Infinium II Assay
  • 1:04:07 40.
    Sequenom MassARRAY iPLEX Platform
  • 1:05:04 41.
    Digital PCR
  • 1:05:42 42.
    Pyrosequencing – SNP and Mutation Analysis
  • 1:06:52 43.
    Exome Sequencing
  • 1:09:47 44.
    Data Analysis and Computation
  • 1:11:44 45.
    Resources & Software Tools
  • 1:12:32 46.
    Resources & Software Tools
  • 1:14:53 47.
    Resources & Software Tools
  • 1:15:19 48.
    Question
  • 1:15:58 49.
    Nomenclature of Cytogenetic Band
  • 1:18:54 50.
    Structural Variants
  • 1:19:54 51.
    Influence of Structural Variants on Phenotype
  • 1:21:27 52.
    Mutation
  • 1:24:15 53.
    Nondisjunction
  • 1:25:24 54.
    Question
  • 1:25:29 55.
    Mosaicism
  • 1:26:50 56.
    Chromothripsis / Kataegis
  • 索引
  • 筆記
  • 討論
  • 全螢幕
Genomic approaches to study DNA structure variation (0427)
長度: 1:27:36, 瀏覽: 847, 最近修訂: 2021-05-05
    上一篇 下一篇
    • 00:00 1.
      index 1
    • 00:11 2.
      Mutation
    • 02:08 3.
      Mutation
    • 03:34 4.
      Nomenclature for RefSeq Accession Number
    • 05:19 5.
      BeadChip Products
    • 06:21 6.
      Characters Used for Describing Seq. Variants
    • 07:16 7.
      Question
    • 08:08 8.
      Characters Used for Describing Seq. Variants
    • 12:11 9.
      Characters Used for Describing Seq. Variants
    • 14:36 10.
      Characters Used for Describing Seq. Variants
    • 17:38 11.
      Examples for Description of Sequence Variants
    • 20:37 12.
      Examples for Description of Sequence Variants
    • 22:12 13.
      Structural Variants
    • 25:32 14.
      Single Nucleotide Polymorphism1
    • 27:17 15.
      Basic Concept of SNPs
    • 27:48 16.
      Single Nucleotide Polymorphism2
    • 29:05 17.
      Phenotype Associated With SNP
    • 29:37 18.
      Mendelian vs. Complex Disease
    • 31:43 19.
      Common Variant vs. Multiple Rare Variant Hypothesis
    • 33:06 20.
      Approaches to Gene Mapping
    • 35:24 21.
      Linkage and Linkage Disequilibrium
    • 37:15 22.
      Association Studies and Linkage Disequilibrium
    • 38:38 23.
      Linkage Disequilibrium1
    • 40:50 24.
      Linkage Disequilibrium2
    • 42:11 25.
      Tag SNP
    • 44:45 26.
      dbSNPhttps://www.ncbi.nlm.nih.gov/snp
    • 45:13 27.
      Genotype-Tissue Expression (GTEx)
    • 46:53 28.
      Summary of Identifying Genetic Variation
    • 48:44 29.
      Haplotype
    • 49:56 30.
      Genome Phasing
    • 51:07 31.
      Loss of Heterozygosity (LOH)
    • 52:32 32.
      Loss of Heterozygosity (LOH)
    • 53:26 33.
      Genome-Wide Association Study (GWAS)
    • 56:02 34.
      Clinical Translation of Findings From Genome-Wide Association Studies
    • 57:06 35.
      Affymetrix Genotyping Assay
    • 59:32 36.
      Illumina Genotyping Beadchip
    • 59:54 37.
      Golden Gate Assay
    • 1:01:54 38.
      Golden Gate Assay
    • 1:02:24 39.
      Infinium II Assay
    • 1:04:07 40.
      Sequenom MassARRAY iPLEX Platform
    • 1:05:04 41.
      Digital PCR
    • 1:05:42 42.
      Pyrosequencing – SNP and Mutation Analysis
    • 1:06:52 43.
      Exome Sequencing
    • 1:09:47 44.
      Data Analysis and Computation
    • 1:11:44 45.
      Resources & Software Tools
    • 1:12:32 46.
      Resources & Software Tools
    • 1:14:53 47.
      Resources & Software Tools
    • 1:15:19 48.
      Question
    • 1:15:58 49.
      Nomenclature of Cytogenetic Band
    • 1:18:54 50.
      Structural Variants
    • 1:19:54 51.
      Influence of Structural Variants on Phenotype
    • 1:21:27 52.
      Mutation
    • 1:24:15 53.
      Nondisjunction
    • 1:25:24 54.
      Question
    • 1:25:29 55.
      Mosaicism
    • 1:26:50 56.
      Chromothripsis / Kataegis
    位置
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    3. 2021
    資料夾名稱
    2021
    發表人
    賴亮全
    單位
    賴亮全教授
    建立
    2021-04-27 16:10:11
    最近修訂
    2021-05-05 12:27:40
    長度
    1:27:36

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