Title Statements
- Full title :Disease Gene Identification : Methods and Protocols / edited by Johanna K. DiStefano.
Summary
This volume presents detailed laboratory procedures in an easy to follow format that can be carried out with success by investigators lacking previous exposure to a specific research method. Chapter guide readers through the application of molecular approaches to disease gene identification and overviews, and case studies are also presented. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, Disease Gene Identification: Methods and Protocols, Second Edition aims to help with the identification and characterization of many more disease-related genes and provide novel, and effective strategies for disease treatment and prevention.
Read More ↓Edition Statements
- Publication Date:2018.
- Edition:2nd ed. 2018
Publication Statements
- Publisher(s):Humana Press, Imprint, Springer New York
- Place of Publication:New York, NY
- Language:eng
- Publication Date:2018.
The Physical Object
- Description:1 online resource (x, 400 pages 63 illustrations, 50 illustrations in color.) : : online resource
Edition Identifiers
- ISBN:9781493974719, 1493974718
- DOI:10.1007/978-1-4939-7471-9
- oclc:on1034540593
- LC Classification:QH431
- Dewey Decimal:611.01816
Table of Contents
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 E…
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