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Sequence Alignment

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Computational Genome Analysis
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Abstract

Much of biology is based on recognition of shared characters among organisms, extending from shared biochemical pathways among eukaryotes to shared skeletal structures among tetrapods. The advent of protein and nucleic acid sequencing in molecular biology made possible comparison of organisms in terms of their DNA or the proteins that DNA encodes. These comparisons are important for a number of reasons. First, they can be used to establish evolutionary relationships among organisms using methods analogous to those employed for anatomical characters. Second, comparison may allow identification of functionally conserved sequences (e.g., DNA sequences controlling gene expression). Finally, such comparisons between humans and other species may identify corresponding genes in model organisms, which can be genetically manipulated to develop models for human diseases.

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References

  • Smith TF, Waterman MS (1981) The identification of common molecular subsequences. Journal of Molecular Biology 147:195–197.

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  • Thompson JD, Higgins DG, Gibson TJ (1994) CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Research 22:4673–4680.

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© 2005 Springer Science+Business Media, Inc.

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(2005). Sequence Alignment. In: Computational Genome Analysis. Springer, New York, NY. https://doi.org/10.1007/0-387-28807-4_6

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  • DOI: https://doi.org/10.1007/0-387-28807-4_6

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-0-387-98785-9

  • Online ISBN: 978-0-387-28807-9

  • eBook Packages: Computer ScienceComputer Science (R0)

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