Disease Gene Identification : Methods and Protocols /
| Autor Corporativo: | |
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| Otros Autores: | |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
New York, NY :
Springer New York : Imprint: Humana,
2018.
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| Edición: | 2nd ed. 2018. |
| Colección: | Methods in Molecular Biology,
1706 |
| Materias: |
Tabla de Contenidos:
- Identification of Disease Susceptibility Alleles in the Next Generation Sequencing Era
- Induced Pluripotent Stem Cells in Disease Modeling and Gene Identification
- Development of Targeted Therapies Based on Gene Modification
- What can we Learn about Human Disease from the Nematode C. elegans?
- Microbiome Sequencing Methods for Studying Human Diseases
- The Emerging Role of Long Noncoding RNAs in Human Disease
- Identification of Disease-related Genes using a Genome-wide Association Study Approach
- Whole Genome Library Construction for Next Generation Sequencing
- Whole Exome Library Construction for Next Generation Sequencing
- Optimized Methodology for the Generation of RNA-sequencing Libraries from Low-input Starting Material: Enabling Analysis of Specialized Cell Types and Clinical Samples
- Using C1 to Generate Single-cell Full-length cDNA Libraries for mRNA Sequencing
- MiSeq: A Next Generation Sequencing Platform for Genomic Analysis
- Methods for CpG Methylation Array Profiling via Bisulfite Conversion
- miRNA Quantification Method using Quantitative Polymerase Chain Reaction in Conjunction with the Cq Method
- Lentiviral
- mediated CRISPR
- cas9 Gene Editing of Primary Human Airway Epithelial Cells
- RNA Interference to Knockdown Gene Expression
- Using Luciferase Reporter Assays to Identify Functional Variants at Disease-associated Loci
- Physiologic Interpretation of GWAS Signals for type 2 Diabetes
- Identification of Genes for Hereditary Hemochromatosis
- Identification of Driver Mutations in Rare Cancers: The Role of SMARCA4 in Small Cell Carcinoma of the Ovary, Hypercalcemic Type (SCCOHT)
- The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression.