Dna Sequencing After the Human Genome Project

Charles R. Cantor Center for Advanced Biotechnology and Departments of Biomedical Engineering, Biology, and Pharmacology and Experimental Therapeutics, Boston University, Boston, MA, 02215, USA

Kai Tang Center for Advanced Biotechnology and Departments of Biomedical Engineering, Biology, and Pharmacology and Experimental Therapeutics, Sequenom, Inc, San Diego

Joel H. Graber Center for Advanced Biotechnology and Departments of Biomedical Engineering, Biology, and Pharmacology and Experimental Therapeutics, Boston University, Boston, MA, 02215, USA

Maryanne Maloney Center for Advanced Biotechnology and Departments of Biomedical Engineering, Biology, and Pharmacology and Experimental Therapeutics, Sequenom, Inc, San Diego

Dong Jing Fu Center for Advanced Biotechnology and Departments of Biomedical Engineering, Biology, and Pharmacology and Experimental Therapeutics, Sequenom, Inc, San Diego

Natalia E. Broude Center for Advanced Biotechnology and Departments of Biomedical Engineering, Biology, and Pharmacology and Experimental Therapeutics, Boston University, Boston, MA, 02215, USA

Fouad Siddiqi Center for Advanced Biotechnology and Departments of Biomedical Engineering, Biology, and Pharmacology and Experimental Therapeutics, Boston University, Boston, MA, 02215, USA

Hubert Koester Department of Chemistry, University of Hamburg

Cassandra L. Smith Center for Advanced Biotechnology and Departments of Biomedical Engineering, Biology, and Pharmacology and Experimental Therapeutics, Boston University, Boston, MA, 02215, USA

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Abstract

In future DNA sequencing, gel electrophoresis, which is particularly effective for de novo sequencing, is likely to be replaced by sequencing by hybridization, mass spectrometry, or combinations of these two methods, which are particularly effective for comparative or diagnostic sequencing.

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Dna Sequencing After the Human Genome Project

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Dna Sequencing After the Human Genome Project

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