Book Volume 838 2012

Genomic Structural Variants

Methods and Protocols

Editors:

ISBN: 978-1-61779-506-0 (Print) 978-1-61779-507-7 (Online)

Table of contents (18 protocols)

  1. Front Matter

    Pages i-xi

  2. No Access

    Protocol

    Pages 1-27

    What Have Studies of Genomic Disorders Taught Us About Our Genome?

  3. No Access

    Protocol

    Pages 29-75

    Microdeletion and Microduplication Syndromes

  4. No Access

    Protocol

    Pages 77-95

    Structural Genomic Variation in Intellectual Disability

  5. No Access

    Protocol

    Pages 97-113

    Copy Number Variation and Psychiatric Disease Risk

  6. No Access

    Protocol

    Pages 115-135

    Detection and Characterization of Copy Number Variation in Autism Spectrum Disorder

  7. No Access

    Protocol

    Pages 137-149

    Structural Variation in Subtelomeres

  8. No Access

    Protocol

    Pages 151-171

    Array-Based Approaches in Prenatal Diagnosis

  9. No Access

    Protocol

    Pages 173-186

    Structural Variation and Its Effect on Expression

  10. No Access

    Protocol

    Pages 187-207

    The Challenges of Studying Complex and Dynamic Regions of the Human Genome

  11. No Access

    Protocol

    Pages 209-223

    Population Genetic Nature of Copy Number Variation

  12. No Access

    Protocol

    Pages 225-248

    Detection and Interpretation of Genomic Structural Variation in Mammals

  13. No Access

    Protocol

    Pages 249-272

    Structural Genetic Variation in the Context of Somatic Mosaicism

  14. No Access

    Protocol

    Pages 273-289

    Online Resources for Genomic Structural Variation

  15. No Access

    Protocol

    Pages 291-310

    Algorithm Implementation for CNV Discovery Using Affymetrix and Illumina SNP Array Data

  16. No Access

    Protocol

    Pages 311-328

    Targeted Screening and Validation of Copy Number Variations

  17. No Access

    Protocol

    Pages 329-341

    High-Resolution Copy Number Profiling by Array CGH Using DNA Isolated from Formalin-Fixed, Paraffin-Embedded Tissues

  18. No Access

    Protocol

    Pages 343-367

    Characterizing and Interpreting Genetic Variation from Personal Genome Sequencing

  19. No Access

    Protocol

    Pages 369-384

    Massively Parallel Sequencing Approaches for Characterization of Structural Variation

  20. Back Matter

    Pages 385-386