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Chromoanagenesis: Methods and Protocols [Kõva köide]

  • Formaat: Hardback, 664 pages, kõrgus x laius: 254x178 mm, 140 Illustrations, color; 9 Illustrations, black and white; IX, 664 p. 149 illus., 140 illus. in color., 1 Hardback
  • Sari: Methods in Molecular Biology 2968
  • Ilmumisaeg: 24-Sep-2025
  • Kirjastus: Springer-Verlag New York Inc.
  • ISBN-10: 1071647490
  • ISBN-13: 9781071647493
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  • Formaat: Hardback, 664 pages, kõrgus x laius: 254x178 mm, 140 Illustrations, color; 9 Illustrations, black and white; IX, 664 p. 149 illus., 140 illus. in color., 1 Hardback
  • Sari: Methods in Molecular Biology 2968
  • Ilmumisaeg: 24-Sep-2025
  • Kirjastus: Springer-Verlag New York Inc.
  • ISBN-10: 1071647490
  • ISBN-13: 9781071647493

This extensive volume explores the phenomena of chaotic genomic rearrangements, known as chromoanagenesis, their formation mechanisms, and the state-of-the-art techniques used to detect them. The book delves into the potential impact of chromoanagenesis on cancers and congenital diseases, as well as its broader implications for genomic evolution and human health through a variety of cutting-edge methodologies. Written for the highly successful Methods in Molecular Biology series, most chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step and readily reproducible laboratory protocols, and tips for troubleshooting and avoiding known pitfalls.

 

Authoritative and comprehensive, Chromoanagenesis: Methods and Protocols serves as an ideal guide to the mechanisms and consequences of chromoanagenesis and a resource for researchers and clinicians seeking to explore the cutting-edge techniques and models used to study this phenomenon.

Chromothripsis.- Chromoanasynthesis.- Chromoplexy.- Chromoanagenesis and
Beyond: Catastrophic Events Shaping the Genome.- Performing SABER-FISH on
Chromosome Spreads in Fixed Tissue Culture Cells and in Tissues.- Genomic
Detection and Delineation of Chromoanasynthesis by Mate-Pair Sequencing.-
Detection of Complex Genomic Rearrangements Using Short-Read Whole Genome
Sequencing in C. elegans.- Hybrid Sequencing Characterization of Complex
Chromosomal Rearrangements.- Combination of Long-Read Sequencing and Hi-C
Technology to Identify Chromoanagenesis Events in Cancer.- Identification and
Characterization of Chromothripsis by Optical Genome Mapping.- Exploring
Chromoanagenesis with DAFCA (Dam Assisted Fluorescent Tagging of Chromatin
Accessibility): Integrating Chromatin Accessibility and Optical Genome
Mapping for Enhanced Structural Variant Detection.- Leveraging Hi-C Data to
Detect Chromosomal Reorganizations.- Chromoanagenesis Detection in Chronic
Lymphocytic Leukemia.- Application and Prospects of Long Read Sequencers for
Preimplantation Genetic Testing for Structural Rearrangements.- Visual
Inspection of Sequencing Data for Diagnosis: Practical Guide to Structural
Variant Analysis Using Integrative Genomics Viewer (IGV).- Artificial
Intelligence and Chromothripsis.- Machine Learning for Detecting and
Analyzing Chromoanagenesis Events.- ISCN and Chromoanagenesis.- Structural
and Mechanistic Diversity of Constitutional Chromoanagenesis.-
Chromoanagenesis in Multiple Myeloma: A Comprehensive Overview.- Origin and
Fate of Micronuclei on the Road to Chromoanagenesis.- The Fate of
Micronuclei.- Transgenerational Tracking of Chromosomes from Micronuclei.-
Investigating Nuclear Envelope Assembly on Mis-Segregated Chromosomes.-
Transcription-Replication Conflicts and Incomplete Replication as a Cause of
Micronuclei-Driven Chromoanagenesis.- DNA Damage, Telomere and Centromere
Dysfunction in Chromothripsis Rearrangements.- Incomplete Trisomic Rescue by
Chromothripsis Leads to Small Supernumerary Marker Chromosomes.- Oligopaint
FISH to Study Chromosomal Architecture and Structural Variations.- Single
Molecule Studies with AFM and High-Speed AFM: From Nucleosomes to
Chromosomes.- Multifocal Genomic Reconstruction Leading to Germline
Structural Variants.- Sperm DNA Fragmentation as a Marker of Chromoanagenesis
Occurrence during Spermatogenesis.- Isolation of Germ Cell Populations from
Mouse Testis by Flow Cytometry.- The Chromatin Configuration Promotes
Constitutional Chromosomal Rearrangements in Post-Meiotic Sperm.-
Recql5-Deficient Mice as a Model for Studying Chromoanagenesis Phenomena.-
Computational Modeling of Chromoanagenesis- or Chromothripsis-Induced SNPs in
Anti-Apoptotic Genes: Their Impact on Protein Structure and Function.-
Chromosomal Instability and Chromoanagenesis as Forces for Genomic
Evolution.- The Evolutionary Potential of Chromoanagenesis.