Abstract
The advent of next generation sequencing technologies has opened new possibilities in the analysis of human disease. In this review we present the main next-generation sequencing technologies, with their major contributions and possible applications to the study of the genetic etiology of complex diseases.
Copyright © 2011 Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Chromosome Mapping / methods
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Chromosome Mapping / trends*
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Genetic Diseases, Inborn / diagnosis
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Genetic Diseases, Inborn / genetics*
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Genetic Diseases, Inborn / physiopathology
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Genetic Predisposition to Disease / genetics*
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Genotyping Techniques / methods
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Genotyping Techniques / trends
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Humans
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Sequence Analysis, DNA / methods
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Sequence Analysis, DNA / trends