New High Throughput Technologies for DNA Sequencing and Genomics
- Keith Mitchelson, Capitalbio Corporation, Beijing, China
New High Throughput Technologies for DNA Sequencing and Genomics is the second volume in the Perspectives in Bioanalysis series, which looks at the electroanalytical chemistry of nucleic acids and proteins, development of electrochemical sensors and their application in biomedicine and in the new fields of genomics and proteomics. The authors have expertly formatted the information for a wide variety of readers, including new developments that will inspire students and young scientists to create new tools for science and medicine in the 21st century.
Reviews of complementary developments in Sanger and SBS sequencing chemistries, capillary electrophoresis and microdevice integration, MS sequencing and applications set the framework for the book.
For students and researchers interested in DNA sequencing technology
- Published: February 2007
- Imprint: ELSEVIER
- ISBN: 978-0-444-52223-8
Table of ContentsEnabling Technologies1. Overview: Developments in DNA Sequencing (K.R. Mitchelson et al.).
2. Chip Capillary Electrophoresis and Total Genetic Analysis Systems (Qiang Xiong, Jing Cheng).
3. Comparative Sequence Analysis by MALDI TOF Mass Spectrometry - Utilizing the Known to Discover the New (M. Ehrich et al.).
4. Advances in Dye-Nucleotide Conjugate Chemistry for DNA Sequencing (Shiv Kumar, C.W. Fuller).Sequencing by Synthesis Platforms5. The 454 Life Sciences Picoliter Sequencing System (M. Margulies et al.).
6. An Integrated System for DNA Sequencing by Synthesis (J. Edwards et al.).Single Molecule Sequencing7. Single Molecule Fluorescence Microscopy and its Applications to Single Molecule Sequencing by Cyclic Synthesis (B. Hebert, I. Braslavsky).
8. Rapid DNA Sequencing by Direct Nanoscale Reading of Nucleotide Bases on Individual DNA Chains (J. Weifu Lee, A. Meller).
9. Optical Sequencing of Single DNA Molecules (D.C. Schwartz et al.).Sequencing Validations and Analysis10. Sequencing Aided by Mutagenesis (SAM) Facilitates the De Novo Sequencing of Megabase DNA Fragments by Short Read Lengths (J.M. Keith et al.).
11. Genome Sequencing and Assembly (A. McGrath).
12. Valid Recovery of Nucleic Acid Sequence Information from High Contamination Risk Samples – Ancient DNA and Environmental DNA (G.A. Kowalchuk et al.).