Epigenome Editing : Methods and Protocols /

Detalles Bibliográficos
Autor Corporativo: SpringerLink (Online service)
Otros Autores: Jeltsch, Albert. (Editor ), Rots, Marianne G. (Editor )
Formato: eBook
Lenguaje:English
Publicado: New York, NY : Springer New York : Imprint: Humana, 2018.
Edición:1st ed. 2018.
Colección:Methods in Molecular Biology, 1767
Materias:
Tabla de Contenidos:
  • Editing the Epigenome: Overview, Open Questions, and Directions of Future Development
  • Zinc Fingers, TALEs and CRISPR Systems: A Comparison of Tools for Epigenome Editing
  • Designing Epigenome Editors: Considerations of Biochemical and Locus Specificities
  • Generation of TALE-Based Designer Epigenome Modifiers
  • Neuroepigenetic Editing
  • Allele-Specific Epigenome Editing
  • Key to Delivery: The (Epi-)Genome Editing Vector Toolbox
  • CRISPR/dCas9 Switch Systems for Temporal Transcriptional Control
  • Delivery of Designer Epigenome Modifiers into Primary Human T Cells
  • Viral Expression of Epigenome Editing Tools in Rodent Brain Using Stereotaxic Surgery Techniques
  • Stable Expression of Epigenome Editors Via Viral Delivery and Genomic Integration
  • Purified-Protein Delivery to Activate an Epigenetically-Silenced Allele in Mouse Brain
  • Non-Viral Methodology for Efficient Co-Transfection
  • Chromatin Immunoprecipitation in Human and Yeast Cells
  • Chromatin Immunoprecipitation and High Throughput Sequencing (ChIP-Seq): Tips and Tricks Regarding the Laboratory Protocol and Initial Downstream Data Analysis
  • Generation of Whole Genome Bisulfite Sequencing Libraries for Comprehensive DNA Methylome Analysis
  • Approaches for the Analysis and Interpretation of Whole Genome Bisulfite Sequencing Data
  • Whole Genome Bisulfite Sequencing for the Analysis of Genome-Wide DNA Methylation and Hydroxymethylation Patterns at Single-Nucleotide Resolution
  • Locus-Specific DNA Methylation Analysis by Targeted Deep Bisulfite Sequencing
  • DNA Methylation Analysis by Bisulfite Conversion Coupled to Double Multiplexed Amplicon-Based Next-Generation Sequencing (NGS)
  • Cell-to-Cell Transcription Variability as Measured by Single Molecule RNA FISH to Detect Epigenetic State Switching
  • Establishment of Cell Lines Stably Expressing dCas-Fusions to Address Kinetics of Epigenetic Editing
  • Editing of DNA Methylation Using dCas9-Peptide Repeat and scFv-TET1 Catalytic Domain Fusions
  • Chemical Inducible dCas9-Guided Editing of H3K27 Acetylation in Mammalian Cells
  • Screening Regulatory Element Function with CRISPR/Cas9-Based Epigenome Editing.