Protocols in Human Molecular Genetics

Front Cover
Springer Science & Business Media, Feb 3, 2008 - Medical - 472 pages
Extraordinary advances have been made in the field of human molecular genetics during the past five years. The ability to amplify a specific region ofDNA a millionfold in a few hours using the polymerase chain reaction has led to the rapid identification of mutations in human disease and of DNA sequence polymorphisms on every human chro- some. DNA fragments of up to 1 megabase in length can now be resolved by pulsed-field gel electrophoresis to create long-range physical maps of important regions of the genome, and can be cloned in the form of yeast artificial chromosomes. The discovery of highly variable "minisatellite" DNA sequences has led to the development of DNA fingerprinting. The application of these techniques to the study of the human genome has culminated in major advances such as the cloning of the cystic fibrosis gene, the construction of genetic linkage maps of each human chro- some, the mapping of many genes responsible for human inherited d- orders, genetic fingerprinting of forensic specimens, and the detection of mutations involved in the development of human tumors. Although many of the new techniques in molecular genetics can be learned relatively easily, it is often difficult for a researcher to obtain all of the relevant information necessary for getting up a technique and applying it successfully. The information available in the research lite- ture often lacks the depth of description that the new user requires.

From inside the book

Contents

Direct DNA Sequencing of Complementary DNA Amplified by
9
Direct Sequencing of PCRAmplified DNA Peter M Green
21
Rapid DNA Sequence Analysis Using Fluorescent Labels
29
Detection of Mutations in DNA and RNA by Chemical Cleavage
39
Rapid Methods for Detection of Polymorphic Markers in Genomic
51
The Analysis of Point Mutations Using Synthetic Oligonucleotide
69
Detection of Mutations by the Amplification Refractory Mutation
77
Automated Gene Detection Using the Oligonucleotide Ligation
85
Yeast ArtificialChromosome YAC Cloning Systems Michele Ramsay
197
Gene Targeting for Somatic Cell Manipulation Julia R Dorin
223
In Situ Hybridization of Chromosomes Kong H Choo Ruth M Brown
233
Methodology and Its Applications
255
DNA Fingerprinting and Forensic Medicine Karen M Sullivan
273
The Detection of Point Mutations in Hemoglobin Defects Using
287
Detection of Gene Deletions Using Multiplex Polymerase
299
Application of PulsedField Gel Electrophoresis to Genetic Diagnosis
313

Detection of Point Mutations by DenaturingGradient
95
The Detection and Mapping of Point Mutations by RNase
111
Discontinuous Polyacrylamide Gel Electrophoresis of
123
Extraction and Enzymatic Amplification of DNA from Paraffin
133
The Use of the Polymerase Chain Reaction in the Mapping
141
An Update Michael R Evans Andrew L Bertera
147
The Detection of Specific DNA Sequences by Enhanced
159
PulsedField Gel Electrophoresis Johan T den Dunnen
169
Cloning from Gels Following PulseField Gel Electrophoresis
183
Molecular Diagnostics of Cancer Bryan D Young
327
The Detection of Latent Virus Infection by Polymerase Chain
347
Mapping Inherited Diseases by Linkage Analysis Martin Farrall
365
Diagnosis of Genetic Disorders with Linked DNA Markers
389
Software for Genetic Linkage Analysis Stephen P Bryant
403
Creating Animal Models of Genetic Diseases Robert P Erickson
419
Ethical Implications
437
Appendix
457
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