Bioinformatics in otolaryngology research. Part two: other high-throughput platforms in genomics and epigenetics

J Laryngol Otol. 2014 Nov;128(11):942-7. doi: 10.1017/S0022215114002011. Epub 2014 Sep 17.

Abstract

Objectives: This second segment of the two-part review summarises several modern high-throughput methods in genomics, epigenetics and molecular biology. Many principles from nucleotide sequencing and transcriptomics can be applied to other high-throughput molecular biology techniques. Specifically, this manuscript reviews: array comparative genome hybridisation; single nucleotide polymorphism arrays; microarray technology, used to study epigenetics; and methodology applied in proteomics. Finally, the review describes current methods for the integration of multiple molecular biology platforms.

Conclusion: Progress in treating human disease in general will require close collaboration with experts in bioinformatics. Improved understanding, by clinicians and physician-scientists in our field, of the concepts presented in both parts of this review will advance diagnosis and therapy for diseases of the head and neck.

Publication types

  • Review

MeSH terms

  • Computational Biology / methods*
  • Epigenomics / methods*
  • Genomics / methods*
  • High-Throughput Nucleotide Sequencing / methods
  • Humans
  • Oligonucleotide Array Sequence Analysis
  • Otolaryngology / methods*
  • Otorhinolaryngologic Diseases / diagnosis
  • Otorhinolaryngologic Diseases / genetics
  • Polymorphism, Single Nucleotide
  • Proteomics